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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2007-01-23 13:54:27 UTC

Update Date

2022-03-07 02:49:29 UTC

HMDB ID

HMDB0005811

Secondary Accession Numbers

HMDB05811

Metabolite Identification

Common Name

Eriocitrin

Description

Eriocitrin, also known as eriodictioside, belongs to the class of organic compounds known as phenylnaphthalenes. Phenylnaphthalenes are compounds containing a phenylnaphthalene skeleton, which consists of a naphthalene bound to a phenyl group. Based on a literature review a significant number of articles have been published on Eriocitrin.

Structure

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

Untitled Document-2
  Mrv0541 02231220302D          

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 17 31  1  6  0  0  0
 14 43  1  6  0  0  0
M  END

HMDB0005811
     RDKit          3D
Eriocitrin
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M  END

Untitled Document-2
  Mrv0541 02231220302D          

 43 47  0  0  0  0            999 V2000
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   -6.2690   -1.3980    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5532   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4111   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2690    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8401    2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4111    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2690    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9822   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3013   -0.0498    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  1  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12  7  1  0  0  0  0
  7 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16  8  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 17  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 23  1  0  0  0  0
 14  4  1  1  0  0  0
 16 29  2  0  0  0  0
  9 30  1  0  0  0  0
 11 31  1  0  0  0  0
 32 33  1  0  0  0  0
  6 34  1  0  0  0  0
  1 35  1  0  0  0  0
 18 36  1  1  0  0  0
 20 37  1  1  0  0  0
 24 33  1  1  0  0  0
 27 38  1  1  0  0  0
 28 39  1  6  0  0  0
 23 40  1  6  0  0  0
 26 41  1  6  0  0  0
 21 32  1  6  0  0  0
 19 42  1  6  0  0  0
 17 31  1  6  0  0  0
 14 43  1  6  0  0  0
M  END
> <DATABASE_ID>
HMDB0005811

> <DATABASE_NAME>
hmdb

> <SMILES>
[H][C@]1(CC(=O)C2=C(C1)C=C(O[C@@H]1O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O)[C@@H](O)[C@H]3O)[C@@H](O)[C@H](O)[C@H]1O)C=C2O)C1=CC=C(O)C(O)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C27H32O15/c28-13-2-1-9(5-14(13)29)10-3-11-4-12(7-16(31)18(11)15(30)6-10)40-27-24(37)20(33)19(32)17(41-27)8-39-26-23(36)21(34)22(35)25(38)42-26/h1-2,4-5,7,10,17,19-29,31-38H,3,6,8H2/t10-,17+,19+,20-,21+,22+,23+,24+,25+,26+,27+/m0/s1

> <INCHI_KEY>
AZXIAVOSESIQNG-SCXABSQUSA-N

> <FORMULA>
C27H32O15

> <MOLECULAR_WEIGHT>
596.534

> <EXACT_MASS>
596.174120354

> <JCHEM_ACCEPTOR_COUNT>
15

> <JCHEM_AVERAGE_POLARIZABILITY>
56.24164140059887

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
10

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3S)-3-(3,4-dihydroxyphenyl)-8-hydroxy-6-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-({[(2R,3R,4R,5R,6R)-3,4,5,6-tetrahydroxyoxan-2-yl]oxy}methyl)oxan-2-yl]oxy}-1,2,3,4-tetrahydronaphthalen-1-one

> <ALOGPS_LOGP>
-0.62

> <JCHEM_LOGP>
-0.635106287999999

> <ALOGPS_LOGS>
-2.16

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.958266588271163

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.14400953756334

> <JCHEM_PKA_STRONGEST_BASIC>
-3.711459377301378

> <JCHEM_POLAR_SURFACE_AREA>
256.28999999999996

> <JCHEM_REFRACTIVITY>
136.51899999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.14e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
eriodictyol 7-O-rutinoside

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0005811
     RDKit          3D
Eriocitrin
 74 78  0  0  0  0  0  0  0  0999 V2000
    5.5851    3.5986   -0.7309 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4992    2.4176   -0.2984 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6275    1.6695    0.2632 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5968    0.2653   -0.3027 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.7099   -0.4963    0.3097 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7173   -1.0520   -0.4567 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7154   -1.7443    0.1873 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7460   -1.9024    1.5630 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7594   -2.6041    2.2053 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.7183   -1.3307    2.2974 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7216   -1.4726    3.6830 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7159   -0.6399    1.6947 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3049   -0.4380    0.0221 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1108    0.4236   -0.2174 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9022   -0.1831   -0.2825 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7102    0.5387   -0.5051 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5126   -0.1285   -0.5617 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7156    0.4787   -0.7751 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5596    0.0782    0.2658 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8351    0.5549    0.1546 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.8974   -0.5330    0.2726 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1410    0.0819    0.1431 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1878   -0.8110    0.2339 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.8622   -0.8154   -0.9857 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0450   -1.5587   -0.9129 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.8111   -2.8595   -0.4699 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0695   -0.9263   -0.0118 C   0  0  2  0  0  0  0  0  0  0  0  0
  -10.1506   -0.4133   -0.6899 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3613    0.1445    0.8015 C   0  0  1  0  0  0  0  0  0  0  0  0
   -9.1663    0.5055    1.8783 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1151   -0.5185    1.3787 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.5263   -1.7389    1.9372 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1013    1.3829   -1.0620 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7296    2.7202   -0.8964 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5509    0.7859   -2.3324 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5240    0.1475   -3.0814 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3696   -0.1221   -2.0396 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5020   -0.0839   -3.1093 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7893    1.8899   -0.6582 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0426    2.5090   -0.5895 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1589    3.8747   -0.7401 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1929    1.7778   -0.3705 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6123    2.0948    0.0470 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4744    1.5633    1.3617 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7476    0.2819   -1.4008 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6850   -0.9235   -1.5287 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.5157   -2.1857   -0.4223 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.4881   -3.0031    1.6209 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.4595   -1.9847    4.1607 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9257   -0.2059    2.3150 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2780   -0.8196    1.0603 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2611   -1.3537   -0.6330 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8029   -1.2604   -0.1645 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6990    1.5598   -0.9018 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0143    1.2269    1.0454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8036   -1.1002    1.2112 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7177   -1.2397   -0.5634 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7324   -1.8272    0.3933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4663   -1.6124   -1.9215 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3388   -3.4094   -1.1218 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4578   -1.6634    0.7359 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1691    0.5698   -0.5296 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0736    1.0135    0.1802 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6647    1.3378    1.7186 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6979    0.1579    2.1261 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0237   -1.6067    2.7799 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2231    1.4084   -1.1977 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4057    3.2222   -0.3706 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1575    1.6291   -2.9420 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2099   -0.7398   -3.4331 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6831   -1.1629   -1.8368 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3921   -0.4015   -2.8530 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9586    2.5426   -0.8313 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3221    4.4194   -0.9009 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 10 12  2  0
  4 13  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 17 18  1  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
 24 25  1  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
 27 29  1  0
 29 30  1  0
 29 31  1  0
 31 32  1  0
 20 33  1  0
 33 34  1  0
 33 35  1  0
 35 36  1  0
 35 37  1  0
 37 38  1  0
 16 39  2  0
 39 40  1  0
 40 41  1  0
 40 42  2  0
 42  2  1  0
 12  5  1  0
 42 14  1  0
 37 18  1  0
 31 23  1  0
  3 43  1  0
  3 44  1  0
  4 45  1  6
  6 46  1  0
  7 47  1  0
  9 48  1  0
 11 49  1  0
 12 50  1  0
 13 51  1  0
 13 52  1  0
 15 53  1  0
 18 54  1  6
 20 55  1  1
 21 56  1  0
 21 57  1  0
 23 58  1  1
 25 59  1  6
 26 60  1  0
 27 61  1  1
 28 62  1  0
 29 63  1  6
 30 64  1  0
 31 65  1  1
 32 66  1  0
 33 67  1  6
 34 68  1  0
 35 69  1  6
 36 70  1  0
 37 71  1  1
 38 72  1  0
 39 73  1  0
 41 74  1  0
M  END

HEADER    PROTEIN                                 23-FEB-12   NONE
TITLE     NULL                                                        
COMPND    MOLECULE: Untitled Document-2                               
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-FEB-12         0                                  
HETATM    1  C   UNK     0     -10.185  -2.342   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -9.196  -3.522   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -7.679  -3.255   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -7.152  -1.807   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -8.142  -0.628   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -9.659  -0.895   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.968  -1.540   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.968  -3.080   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.635  -3.850   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.301  -3.080   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.301  -1.540   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.635  -0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -4.302  -0.770   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -5.636  -1.540   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -5.636  -3.080   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -4.302  -3.850   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.366  -1.540   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.366  -3.080   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.700  -3.850   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.034  -3.080   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.034  -1.540   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       3.700  -0.770   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       7.701   3.080   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       7.701   1.540   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       9.035   0.770   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      10.368   1.540   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      10.368   3.080   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       9.035   3.850   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -4.302  -5.390   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      -1.635  -5.390   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       1.033  -0.770   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       6.367  -0.770   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       6.367   0.770   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0     -10.649   0.285   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0     -11.702  -2.610   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0       1.033  -3.850   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0       6.367  -3.850   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0      11.702   3.850   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0       9.035   5.390   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0       6.367   3.850   0.000  0.00  0.00           O+0
HETATM   41  O   UNK     0      11.702   0.770   0.000  0.00  0.00           O+0
HETATM   42  O   UNK     0       3.700  -5.390   0.000  0.00  0.00           O+0
HETATM   43  H   UNK     0      -6.162  -0.093   0.000  0.00  0.00           H+0
CONECT    1    2    6   35                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   14                                                  
CONECT    5    4    6                                                       
CONECT    6    5    1   34                                                  
CONECT    7    8   12   13                                                  
CONECT    8    7    9   16                                                  
CONECT    9    8   10   30                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   31                                                  
CONECT   12   11    7                                                       
CONECT   13    7   14                                                       
CONECT   14   13   15    4   43                                             
CONECT   15   14   16                                                       
CONECT   16   15    8   29                                                  
CONECT   17   18   22   31                                                  
CONECT   18   17   19   36                                                  
CONECT   19   18   20   42                                                  
CONECT   20   19   21   37                                                  
CONECT   21   20   22   32                                                  
CONECT   22   21   17                                                       
CONECT   23   24   28   40                                                  
CONECT   24   23   25   33                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   41                                                  
CONECT   27   26   28   38                                                  
CONECT   28   27   23   39                                                  
CONECT   29   16                                                            
CONECT   30    9                                                            
CONECT   31   11   17                                                       
CONECT   32   33   21                                                       
CONECT   33   32   24                                                       
CONECT   34    6                                                            
CONECT   35    1                                                            
CONECT   36   18                                                            
CONECT   37   20                                                            
CONECT   38   27                                                            
CONECT   39   28                                                            
CONECT   40   23                                                            
CONECT   41   26                                                            
CONECT   42   19                                                            
CONECT   43   14                                                            
MASTER        0    0    0    0    0    0    0    0   43    0   94    0
END

COMPND    HMDB0005811
HETATM    1  O1  UNL     1       5.585   3.599  -0.731  1.00  0.00           O  
HETATM    2  C1  UNL     1       5.499   2.418  -0.298  1.00  0.00           C  
HETATM    3  C2  UNL     1       6.627   1.670   0.263  1.00  0.00           C  
HETATM    4  C3  UNL     1       6.597   0.265  -0.303  1.00  0.00           C  
HETATM    5  C4  UNL     1       7.710  -0.496   0.310  1.00  0.00           C  
HETATM    6  C5  UNL     1       8.717  -1.052  -0.457  1.00  0.00           C  
HETATM    7  C6  UNL     1       9.715  -1.744   0.187  1.00  0.00           C  
HETATM    8  C7  UNL     1       9.746  -1.902   1.563  1.00  0.00           C  
HETATM    9  O2  UNL     1      10.759  -2.604   2.205  1.00  0.00           O  
HETATM   10  C8  UNL     1       8.718  -1.331   2.297  1.00  0.00           C  
HETATM   11  O3  UNL     1       8.722  -1.473   3.683  1.00  0.00           O  
HETATM   12  C9  UNL     1       7.716  -0.640   1.695  1.00  0.00           C  
HETATM   13  C10 UNL     1       5.305  -0.438   0.022  1.00  0.00           C  
HETATM   14  C11 UNL     1       4.111   0.424  -0.217  1.00  0.00           C  
HETATM   15  C12 UNL     1       2.902  -0.183  -0.282  1.00  0.00           C  
HETATM   16  C13 UNL     1       1.710   0.539  -0.505  1.00  0.00           C  
HETATM   17  O4  UNL     1       0.513  -0.129  -0.562  1.00  0.00           O  
HETATM   18  C14 UNL     1      -0.716   0.479  -0.775  1.00  0.00           C  
HETATM   19  O5  UNL     1      -1.560   0.078   0.266  1.00  0.00           O  
HETATM   20  C15 UNL     1      -2.835   0.555   0.155  1.00  0.00           C  
HETATM   21  C16 UNL     1      -3.897  -0.533   0.273  1.00  0.00           C  
HETATM   22  O6  UNL     1      -5.141   0.082   0.143  1.00  0.00           O  
HETATM   23  C17 UNL     1      -6.188  -0.811   0.234  1.00  0.00           C  
HETATM   24  O7  UNL     1      -6.862  -0.815  -0.986  1.00  0.00           O  
HETATM   25  C18 UNL     1      -8.045  -1.559  -0.913  1.00  0.00           C  
HETATM   26  O8  UNL     1      -7.811  -2.860  -0.470  1.00  0.00           O  
HETATM   27  C19 UNL     1      -9.069  -0.926  -0.012  1.00  0.00           C  
HETATM   28  O9  UNL     1     -10.151  -0.413  -0.690  1.00  0.00           O  
HETATM   29  C20 UNL     1      -8.361   0.144   0.802  1.00  0.00           C  
HETATM   30  O10 UNL     1      -9.166   0.505   1.878  1.00  0.00           O  
HETATM   31  C21 UNL     1      -7.115  -0.519   1.379  1.00  0.00           C  
HETATM   32  O11 UNL     1      -7.526  -1.739   1.937  1.00  0.00           O  
HETATM   33  C22 UNL     1      -3.101   1.383  -1.062  1.00  0.00           C  
HETATM   34  O12 UNL     1      -2.730   2.720  -0.896  1.00  0.00           O  
HETATM   35  C23 UNL     1      -2.551   0.786  -2.332  1.00  0.00           C  
HETATM   36  O13 UNL     1      -3.524   0.148  -3.081  1.00  0.00           O  
HETATM   37  C24 UNL     1      -1.370  -0.122  -2.040  1.00  0.00           C  
HETATM   38  O14 UNL     1      -0.502  -0.084  -3.109  1.00  0.00           O  
HETATM   39  C25 UNL     1       1.789   1.890  -0.658  1.00  0.00           C  
HETATM   40  C26 UNL     1       3.043   2.509  -0.590  1.00  0.00           C  
HETATM   41  O15 UNL     1       3.159   3.875  -0.740  1.00  0.00           O  
HETATM   42  C27 UNL     1       4.193   1.778  -0.371  1.00  0.00           C  
HETATM   43  H1  UNL     1       7.612   2.095   0.047  1.00  0.00           H  
HETATM   44  H2  UNL     1       6.474   1.563   1.362  1.00  0.00           H  
HETATM   45  H3  UNL     1       6.748   0.282  -1.401  1.00  0.00           H  
HETATM   46  H4  UNL     1       8.685  -0.924  -1.529  1.00  0.00           H  
HETATM   47  H5  UNL     1      10.516  -2.186  -0.422  1.00  0.00           H  
HETATM   48  H6  UNL     1      11.488  -3.003   1.621  1.00  0.00           H  
HETATM   49  H7  UNL     1       9.460  -1.985   4.161  1.00  0.00           H  
HETATM   50  H8  UNL     1       6.926  -0.206   2.315  1.00  0.00           H  
HETATM   51  H9  UNL     1       5.278  -0.820   1.060  1.00  0.00           H  
HETATM   52  H10 UNL     1       5.261  -1.354  -0.633  1.00  0.00           H  
HETATM   53  H11 UNL     1       2.803  -1.260  -0.164  1.00  0.00           H  
HETATM   54  H12 UNL     1      -0.699   1.560  -0.902  1.00  0.00           H  
HETATM   55  H13 UNL     1      -3.014   1.227   1.045  1.00  0.00           H  
HETATM   56  H14 UNL     1      -3.804  -1.100   1.211  1.00  0.00           H  
HETATM   57  H15 UNL     1      -3.718  -1.240  -0.563  1.00  0.00           H  
HETATM   58  H16 UNL     1      -5.732  -1.827   0.393  1.00  0.00           H  
HETATM   59  H17 UNL     1      -8.466  -1.612  -1.922  1.00  0.00           H  
HETATM   60  H18 UNL     1      -7.339  -3.409  -1.122  1.00  0.00           H  
HETATM   61  H19 UNL     1      -9.458  -1.663   0.736  1.00  0.00           H  
HETATM   62  H20 UNL     1     -10.169   0.570  -0.530  1.00  0.00           H  
HETATM   63  H21 UNL     1      -8.074   1.013   0.180  1.00  0.00           H  
HETATM   64  H22 UNL     1      -9.665   1.338   1.719  1.00  0.00           H  
HETATM   65  H23 UNL     1      -6.698   0.158   2.126  1.00  0.00           H  
HETATM   66  H24 UNL     1      -8.024  -1.607   2.780  1.00  0.00           H  
HETATM   67  H25 UNL     1      -4.223   1.408  -1.198  1.00  0.00           H  
HETATM   68  H26 UNL     1      -3.406   3.222  -0.371  1.00  0.00           H  
HETATM   69  H27 UNL     1      -2.158   1.629  -2.942  1.00  0.00           H  
HETATM   70  H28 UNL     1      -3.210  -0.740  -3.433  1.00  0.00           H  
HETATM   71  H29 UNL     1      -1.683  -1.163  -1.837  1.00  0.00           H  
HETATM   72  H30 UNL     1       0.392  -0.402  -2.853  1.00  0.00           H  
HETATM   73  H31 UNL     1       0.959   2.543  -0.831  1.00  0.00           H  
HETATM   74  H32 UNL     1       2.322   4.419  -0.901  1.00  0.00           H  
CONECT    1    2    2
CONECT    2    3   42
CONECT    3    4   43   44
CONECT    4    5   13   45
CONECT    5    6    6   12
CONECT    6    7   46
CONECT    7    8    8   47
CONECT    8    9   10
CONECT    9   48
CONECT   10   11   12   12
CONECT   11   49
CONECT   12   50
CONECT   13   14   51   52
CONECT   14   15   15   42
CONECT   15   16   53
CONECT   16   17   39   39
CONECT   17   18
CONECT   18   19   37   54
CONECT   19   20
CONECT   20   21   33   55
CONECT   21   22   56   57
CONECT   22   23
CONECT   23   24   31   58
CONECT   24   25
CONECT   25   26   27   59
CONECT   26   60
CONECT   27   28   29   61
CONECT   28   62
CONECT   29   30   31   63
CONECT   30   64
CONECT   31   32   65
CONECT   32   66
CONECT   33   34   35   67
CONECT   34   68
CONECT   35   36   37   69
CONECT   36   70
CONECT   37   38   71
CONECT   38   72
CONECT   39   40   73
CONECT   40   41   42   42
CONECT   41   74
END

HMDB0005811
     RDKit          3D
Eriocitrin
 74 78  0  0  0  0  0  0  0  0999 V2000
    5.5851    3.5986   -0.7309 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4992    2.4176   -0.2984 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6275    1.6695    0.2632 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5968    0.2653   -0.3027 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.7099   -0.4963    0.3097 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7173   -1.0520   -0.4567 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7154   -1.7443    0.1873 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7460   -1.9024    1.5630 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7594   -2.6041    2.2053 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.7183   -1.3307    2.2974 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7216   -1.4726    3.6830 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7159   -0.6399    1.6947 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3049   -0.4380    0.0221 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1108    0.4236   -0.2174 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9022   -0.1831   -0.2825 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7102    0.5387   -0.5051 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5126   -0.1285   -0.5617 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7156    0.4787   -0.7751 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5596    0.0782    0.2658 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8351    0.5549    0.1546 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.8974   -0.5330    0.2726 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1410    0.0819    0.1431 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1878   -0.8110    0.2339 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.8622   -0.8154   -0.9857 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0450   -1.5587   -0.9129 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.8111   -2.8595   -0.4699 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0695   -0.9263   -0.0118 C   0  0  2  0  0  0  0  0  0  0  0  0
  -10.1506   -0.4133   -0.6899 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3613    0.1445    0.8015 C   0  0  1  0  0  0  0  0  0  0  0  0
   -9.1663    0.5055    1.8783 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1151   -0.5185    1.3787 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.5263   -1.7389    1.9372 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1013    1.3829   -1.0620 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7296    2.7202   -0.8964 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5509    0.7859   -2.3324 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5240    0.1475   -3.0814 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3696   -0.1221   -2.0396 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5020   -0.0839   -3.1093 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7893    1.8899   -0.6582 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0426    2.5090   -0.5895 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1589    3.8747   -0.7401 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1929    1.7778   -0.3705 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6123    2.0948    0.0470 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4744    1.5633    1.3617 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7476    0.2819   -1.4008 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6850   -0.9235   -1.5287 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.5157   -2.1857   -0.4223 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.4881   -3.0031    1.6209 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.4595   -1.9847    4.1607 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9257   -0.2059    2.3150 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2780   -0.8196    1.0603 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2611   -1.3537   -0.6330 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8029   -1.2604   -0.1645 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6990    1.5598   -0.9018 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0143    1.2269    1.0454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8036   -1.1002    1.2112 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7177   -1.2397   -0.5634 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7324   -1.8272    0.3933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4663   -1.6124   -1.9215 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3388   -3.4094   -1.1218 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4578   -1.6634    0.7359 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1691    0.5698   -0.5296 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0736    1.0135    0.1802 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6647    1.3378    1.7186 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6979    0.1579    2.1261 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0237   -1.6067    2.7799 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2231    1.4084   -1.1977 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4057    3.2222   -0.3706 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1575    1.6291   -2.9420 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2099   -0.7398   -3.4331 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6831   -1.1629   -1.8368 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3921   -0.4015   -2.8530 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9586    2.5426   -0.8313 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3221    4.4194   -0.9009 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 10 12  2  0
  4 13  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 17 18  1  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
 24 25  1  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
 27 29  1  0
 29 30  1  0
 29 31  1  0
 31 32  1  0
 20 33  1  0
 33 34  1  0
 33 35  1  0
 35 36  1  0
 35 37  1  0
 37 38  1  0
 16 39  2  0
 39 40  1  0
 40 41  1  0
 40 42  2  0
 42  2  1  0
 12  5  1  0
 42 14  1  0
 37 18  1  0
 31 23  1  0
  3 43  1  0
  3 44  1  0
  4 45  1  6
  6 46  1  0
  7 47  1  0
  9 48  1  0
 11 49  1  0
 12 50  1  0
 13 51  1  0
 13 52  1  0
 15 53  1  0
 18 54  1  6
 20 55  1  1
 21 56  1  0
 21 57  1  0
 23 58  1  1
 25 59  1  6
 26 60  1  0
 27 61  1  1
 28 62  1  0
 29 63  1  6
 30 64  1  0
 31 65  1  1
 32 66  1  0
 33 67  1  6
 34 68  1  0
 35 69  1  6
 36 70  1  0
 37 71  1  1
 38 72  1  0
 39 73  1  0
 41 74  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
Eriodictioside	HMDB
Eriodictyol 7-O-rutinoside	HMDB

Chemical Formula

C₂₇H₃₂O₁₅

Average Molecular Weight

596.534

Monoisotopic Molecular Weight

596.174120354

IUPAC Name

(3S)-3-(3,4-dihydroxyphenyl)-8-hydroxy-6-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-({[(2R,3R,4R,5R,6R)-3,4,5,6-tetrahydroxyoxan-2-yl]oxy}methyl)oxan-2-yl]oxy}-1,2,3,4-tetrahydronaphthalen-1-one

Traditional Name

eriodictyol 7-O-rutinoside

CAS Registry Number

13463-28-0

SMILES

[H][C@]1(CC(=O)C2=C(C1)C=C(O[C@@H]1O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O)[C@@H](O)[C@H]3O)[C@@H](O)[C@H](O)[C@H]1O)C=C2O)C1=CC=C(O)C(O)=C1

InChI Identifier

InChI=1S/C27H32O15/c28-13-2-1-9(5-14(13)29)10-3-11-4-12(7-16(31)18(11)15(30)6-10)40-27-24(37)20(33)19(32)17(41-27)8-39-26-23(36)21(34)22(35)25(38)42-26/h1-2,4-5,7,10,17,19-29,31-38H,3,6,8H2/t10-,17+,19+,20-,21+,22+,23+,24+,25+,26+,27+/m0/s1

InChI Key

AZXIAVOSESIQNG-SCXABSQUSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenylnaphthalenes. Phenylnaphthalenes are compounds containing a phenylnaphthalene skeleton, which consists of a naphthalene bound to a phenyl group.

Kingdom

Super Class

Class

Sub Class

Direct Parent

Alternative Parents

Substituents

Phenylnaphthalene
Phenolic glycoside
Disaccharide
Glycosyl compound
O-glycosyl compound
Tetralin
Catechol
Aryl alkyl ketone
Aryl ketone
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Monocyclic benzene moiety
Oxane
Vinylogous acid
Secondary alcohol
Hemiacetal
Ketone
Acetal
Oxacycle
Organoheterocyclic compound
Polyol
Hydrocarbon derivative
Organic oxide
Alcohol
Organic oxygen compound
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Not Available

Lemon (FooDB: FOOD00054)
Lime (FooDB: FOOD00053)

Milk and milk product

Unfermented milk

Milk (Cow) (FooDB: FOOD00618)

Process

Not Available

Role

Not Available

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	956.90 °C. @ 760.00 mm Hg (est)	The Good Scents Company Information System
Water Solubility	4787 mg/L @ 25 °C (est)	The Good Scents Company Information System
LogP	1.470 (est)	The Good Scents Company Information System

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	4.14 g/L	ALOGPS
logP	-0.62	ALOGPS
logP	-0.64	ChemAxon
logS	-2.2	ALOGPS
pKa (Strongest Acidic)	9.14	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	15	ChemAxon
Hydrogen Donor Count	10	ChemAxon
Polar Surface Area	256.29 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	136.52 m³·mol⁻¹	ChemAxon
Polarizability	56.24 Å³	ChemAxon
Number of Rings	5	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]+	220.341	30932474
DeepCCS	[M-H]-	218.446	30932474
DeepCCS	[M-2H]-	252.461	30932474
DeepCCS	[M+Na]+	226.482	30932474
AllCCS	[M+H]+	229.3	32859911
AllCCS	[M+H-H2O]+	228.2	32859911
AllCCS	[M+NH4]+	230.3	32859911
AllCCS	[M+Na]+	230.6	32859911
AllCCS	[M-H]-	222.3	32859911
AllCCS	[M+Na-2H]-	224.4	32859911
AllCCS	[M+HCOO]-	227.0	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Eriocitrin	[H][C@]1(CC(=O)C2=C(C1)C=C(O[C@@H]1O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O)[C@@H](O)[C@H]3O)[C@@H](O)[C@H](O)[C@H]1O)C=C2O)C1=CC=C(O)C(O)=C1	5540.2	Standard polar	33892256
Eriocitrin	[H][C@]1(CC(=O)C2=C(C1)C=C(O[C@@H]1O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O)[C@@H](O)[C@H]3O)[C@@H](O)[C@H](O)[C@H]1O)C=C2O)C1=CC=C(O)C(O)=C1	4935.0	Standard non polar	33892256
Eriocitrin	[H][C@]1(CC(=O)C2=C(C1)C=C(O[C@@H]1O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O)[C@@H](O)[C@H]3O)[C@@H](O)[C@H](O)[C@H]1O)C=C2O)C1=CC=C(O)C(O)=C1	5452.8	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Eriocitrin,1TMS,isomer #1	C[Si](C)(C)O[C@@H]1O[C@@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5183.6	Semi standard non polar	33892256
Eriocitrin,1TMS,isomer #10	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)=CC=C1O	5175.7	Semi standard non polar	33892256
Eriocitrin,1TMS,isomer #2	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)[C@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O)[C@@H](O)[C@@H]2O)O[C@H]1O	5181.1	Semi standard non polar	33892256
Eriocitrin,1TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](O)O[C@@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O)[C@@H](O)[C@@H]2O)[C@@H]1O	5167.5	Semi standard non polar	33892256
Eriocitrin,1TMS,isomer #4	C[Si](C)(C)O[C@H]1[C@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O)[C@@H](O)[C@@H]2O)O[C@@H](O)[C@H](O)[C@H]1O	5187.7	Semi standard non polar	33892256
Eriocitrin,1TMS,isomer #5	C[Si](C)(C)O[C@@H]1[C@@H](CO[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O)O[C@@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)[C@H](O)[C@H]1O	5199.8	Semi standard non polar	33892256
Eriocitrin,1TMS,isomer #6	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@H](CO[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O)[C@H]1O	5182.7	Semi standard non polar	33892256
Eriocitrin,1TMS,isomer #7	C[Si](C)(C)O[C@H]1[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@H](CO[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O)[C@@H](O)[C@@H]1O	5188.9	Semi standard non polar	33892256
Eriocitrin,1TMS,isomer #8	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O)[C@@H](O)[C@H]3O)[C@@H](O)[C@H](O)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	5154.0	Semi standard non polar	33892256
Eriocitrin,1TMS,isomer #9	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)C=C1O	5171.8	Semi standard non polar	33892256
Eriocitrin,2TMS,isomer #1	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]3O)[C@@H](O)[C@H](O)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	5073.1	Semi standard non polar	33892256
Eriocitrin,2TMS,isomer #10	C[Si](C)(C)O[C@H]1[C@@H](O)[C@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O)[C@@H](O)[C@@H]2O)O[C@@H](O)[C@@H]1O[Si](C)(C)C	5102.7	Semi standard non polar	33892256
Eriocitrin,2TMS,isomer #11	C[Si](C)(C)O[C@H]1[C@H](O)O[C@@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@@H]1O	5106.7	Semi standard non polar	33892256
Eriocitrin,2TMS,isomer #12	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O)[C@@H](O)[C@H](O)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	5084.0	Semi standard non polar	33892256
Eriocitrin,2TMS,isomer #13	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)C=C1O	5062.7	Semi standard non polar	33892256
Eriocitrin,2TMS,isomer #14	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)=CC=C1O	5073.3	Semi standard non polar	33892256
Eriocitrin,2TMS,isomer #15	C[Si](C)(C)O[C@H]1[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@H](CO[C@@H]2O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)[C@@H](O)[C@@H]1O	5109.8	Semi standard non polar	33892256
Eriocitrin,2TMS,isomer #16	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@H](CO[C@@H]2O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)[C@H]1O	5090.5	Semi standard non polar	33892256
Eriocitrin,2TMS,isomer #17	C[Si](C)(C)O[C@@H]1[C@@H](CO[C@@H]2O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)O[C@@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)[C@H](O)[C@H]1O	5113.1	Semi standard non polar	33892256
Eriocitrin,2TMS,isomer #18	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O)[C@@H](O)[C@H](O)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	5068.7	Semi standard non polar	33892256
Eriocitrin,2TMS,isomer #19	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)C=C1O	5034.4	Semi standard non polar	33892256
Eriocitrin,2TMS,isomer #2	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)C=C1O	5086.8	Semi standard non polar	33892256
Eriocitrin,2TMS,isomer #20	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)=CC=C1O	5047.4	Semi standard non polar	33892256
Eriocitrin,2TMS,isomer #21	C[Si](C)(C)O[C@H]1[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@H](CO[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)[C@@H](O)[C@@H]1O	5098.8	Semi standard non polar	33892256
Eriocitrin,2TMS,isomer #22	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@H](CO[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)[C@H]1O	5074.3	Semi standard non polar	33892256
Eriocitrin,2TMS,isomer #23	C[Si](C)(C)O[C@@H]1[C@@H](CO[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)[C@H](O)[C@H]1O	5101.7	Semi standard non polar	33892256
Eriocitrin,2TMS,isomer #24	C[Si](C)(C)O[C@H]1[C@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O)[C@@H](O)[C@@H]2O)O[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	5117.3	Semi standard non polar	33892256
Eriocitrin,2TMS,isomer #25	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	5082.6	Semi standard non polar	33892256
Eriocitrin,2TMS,isomer #26	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)C=C1O	5047.9	Semi standard non polar	33892256
Eriocitrin,2TMS,isomer #27	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)=CC=C1O	5059.7	Semi standard non polar	33892256
Eriocitrin,2TMS,isomer #28	C[Si](C)(C)O[C@H]1[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@H](CO[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@@H](O)[C@@H]1O	5109.8	Semi standard non polar	33892256
Eriocitrin,2TMS,isomer #29	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@H](CO[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@H]1O	5088.3	Semi standard non polar	33892256
Eriocitrin,2TMS,isomer #3	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)=CC=C1O	5100.3	Semi standard non polar	33892256
Eriocitrin,2TMS,isomer #30	C[Si](C)(C)O[C@@H]1[C@@H](CO[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)[C@H](O)[C@H]1O	5113.1	Semi standard non polar	33892256
Eriocitrin,2TMS,isomer #31	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O)[C@@H](O)[C@H]3O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	5096.9	Semi standard non polar	33892256
Eriocitrin,2TMS,isomer #32	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C=C3C2)C=C1O	5074.9	Semi standard non polar	33892256
Eriocitrin,2TMS,isomer #33	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C=C3C2)=CC=C1O	5088.5	Semi standard non polar	33892256
Eriocitrin,2TMS,isomer #34	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@@H]1CO[C@@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@H]1O	5125.1	Semi standard non polar	33892256
Eriocitrin,2TMS,isomer #35	C[Si](C)(C)O[C@@H]1[C@@H](CO[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O)O[C@@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)[C@H](O)[C@H]1O[Si](C)(C)C	5122.0	Semi standard non polar	33892256
Eriocitrin,2TMS,isomer #36	C[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C)[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@H](CO[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O)[C@H]1O	5115.4	Semi standard non polar	33892256
Eriocitrin,2TMS,isomer #37	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O)[C@@H](O)[C@H]3O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	5071.3	Semi standard non polar	33892256
Eriocitrin,2TMS,isomer #38	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3C2)C=C1O	5032.8	Semi standard non polar	33892256
Eriocitrin,2TMS,isomer #39	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3C2)=CC=C1O	5047.4	Semi standard non polar	33892256
Eriocitrin,2TMS,isomer #4	C[Si](C)(C)O[C@@H]1O[C@@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5101.8	Semi standard non polar	33892256
Eriocitrin,2TMS,isomer #40	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O)[C@@H](O)[C@H]3O)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	5091.6	Semi standard non polar	33892256
Eriocitrin,2TMS,isomer #41	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3C2)C=C1O	5050.5	Semi standard non polar	33892256
Eriocitrin,2TMS,isomer #42	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3C2)=CC=C1O	5063.8	Semi standard non polar	33892256
Eriocitrin,2TMS,isomer #43	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3O[Si](C)(C)C)C2)C=C1O	5055.9	Semi standard non polar	33892256
Eriocitrin,2TMS,isomer #44	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3O[Si](C)(C)C)C2)=CC=C1O	5071.6	Semi standard non polar	33892256
Eriocitrin,2TMS,isomer #45	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)C=C1O[Si](C)(C)C	5096.9	Semi standard non polar	33892256
Eriocitrin,2TMS,isomer #5	C[Si](C)(C)O[C@@H]1O[C@@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5078.1	Semi standard non polar	33892256
Eriocitrin,2TMS,isomer #6	C[Si](C)(C)O[C@@H]1O[C@@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5106.2	Semi standard non polar	33892256
Eriocitrin,2TMS,isomer #7	C[Si](C)(C)O[C@@H]1O[C@@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	5096.1	Semi standard non polar	33892256
Eriocitrin,2TMS,isomer #8	C[Si](C)(C)O[C@@H]1O[C@@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	5090.2	Semi standard non polar	33892256
Eriocitrin,2TMS,isomer #9	C[Si](C)(C)O[C@@H]1O[C@@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	5104.3	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #1	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O)[C@@H](O)[C@H](O)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4974.6	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #10	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)C=C1O	4956.5	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #100	C[Si](C)(C)O[C@H]1[C@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]1O	4995.4	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #101	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O)[C@@H](O)[C@H]3O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4989.7	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #102	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O)[C@@H](O)[C@H]3O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	5003.1	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #103	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C=C3O[Si](C)(C)C)C2)C=C1O	4964.8	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #104	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C=C3O[Si](C)(C)C)C2)=CC=C1O	4977.5	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #105	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3C2)C=C1O	4949.8	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #106	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3C2)C=C1O	4965.7	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #107	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C=C3C2)C=C1O[Si](C)(C)C	5027.0	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #108	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3C2)=CC=C1O	4956.3	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #109	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3C2)=CC=C1O	4966.3	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #11	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)C=C1O	4965.2	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #110	C[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C)[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@H](CO[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O)[C@H]1O[Si](C)(C)C	5036.2	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #111	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O)[C@@H](O)[C@H]3O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4995.9	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #112	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C=C3C2)C=C1O	4952.9	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #113	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C=C3C2)=CC=C1O	4961.7	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #114	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3O[Si](C)(C)C)C2)C=C1O	4929.9	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #115	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3O[Si](C)(C)C)C2)=CC=C1O	4947.7	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #116	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3C2)C=C1O[Si](C)(C)C	4993.7	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #117	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3O[Si](C)(C)C)C2)C=C1O	4963.0	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #118	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3O[Si](C)(C)C)C2)=CC=C1O	4980.7	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #119	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3C2)C=C1O[Si](C)(C)C	5019.6	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #12	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C=C3C2)C=C1O	4974.7	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #120	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3O[Si](C)(C)C)C2)C=C1O[Si](C)(C)C	5010.2	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #13	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3C2)C=C1O	4937.7	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #14	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3C2)C=C1O	4968.0	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #15	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)C=C1O[Si](C)(C)C	5038.0	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #16	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)=CC=C1O	4986.7	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #17	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)=CC=C1O	4967.6	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #18	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)=CC=C1O	4973.8	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #19	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C=C3C2)=CC=C1O	4975.8	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #2	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O)[C@@H](O)[C@H](O)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4964.8	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #20	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3C2)=CC=C1O	4948.8	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #21	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3C2)=CC=C1O	4973.0	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #22	C[Si](C)(C)O[C@@H]1O[C@@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	4976.2	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #23	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@@H]1CO[C@@H]1O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]1O	4988.9	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #24	C[Si](C)(C)O[C@@H]1O[C@@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4981.0	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #25	C[Si](C)(C)O[C@@H]1O[C@@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4976.6	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #26	C[Si](C)(C)O[C@@H]1O[C@@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4995.0	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #27	C[Si](C)(C)O[C@@H]1O[C@@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4976.6	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #28	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@H](CO[C@@H]2O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@H]1O	4945.3	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #29	C[Si](C)(C)O[C@@H]1O[C@@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4943.4	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #3	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4964.4	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #30	C[Si](C)(C)O[C@@H]1O[C@@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4956.4	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #31	C[Si](C)(C)O[C@@H]1[C@@H](CO[C@@H]2O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)[C@H](O)[C@H]1O	4977.6	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #32	C[Si](C)(C)O[C@@H]1O[C@@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4972.2	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #33	C[Si](C)(C)O[C@@H]1O[C@@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4986.8	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #34	C[Si](C)(C)O[C@@H]1O[C@@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4984.0	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #35	C[Si](C)(C)O[C@@H]1O[C@@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4984.2	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #36	C[Si](C)(C)O[C@@H]1O[C@@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4984.2	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #37	C[Si](C)(C)O[C@H]1[C@H](O)O[C@@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	5015.9	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #38	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O)[C@@H](O)[C@H](O)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4985.3	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #39	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)C=C1O	4928.8	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #4	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]3O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4968.0	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #40	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)=CC=C1O	4947.0	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #41	C[Si](C)(C)O[C@H]1[C@@H](O)[C@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]2O)O[C@@H](O)[C@@H]1O[Si](C)(C)C	4996.8	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #42	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@H](CO[C@@H]2O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O)[C@H]1O	4957.0	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #43	C[Si](C)(C)O[C@@H]1[C@@H](CO[C@@H]2O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)[C@H](O)[C@H]1O	4991.3	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #44	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4993.9	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #45	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)C=C1O	4934.3	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #46	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)=CC=C1O	4951.1	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #47	C[Si](C)(C)O[C@H]1[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@H](CO[C@@H]2O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@@H](O)[C@@H]1O	5002.0	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #48	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@H](CO[C@@H]2O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@H]1O	4970.1	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #49	C[Si](C)(C)O[C@@H]1[C@@H](CO[C@@H]2O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)[C@H](O)[C@H]1O	4999.1	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #5	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]3O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4949.1	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #50	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4995.0	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #51	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4969.9	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #52	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	5004.1	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #53	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3O[Si](C)(C)C)C2)C=C1O	4961.7	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #54	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3O[Si](C)(C)C)C2)=CC=C1O	4975.3	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #55	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C=C3C2)C=C1O	4945.4	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #56	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3C2)C=C1O	4910.2	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #57	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3C2)C=C1O	4939.6	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #58	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)C=C1O[Si](C)(C)C	5023.8	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #59	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C=C3C2)=CC=C1O	4948.8	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #6	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]3O)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4975.4	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #60	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3C2)=CC=C1O	4919.3	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #61	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3C2)=CC=C1O	4946.7	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #62	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@@H]1CO[C@@H]1O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O	5009.5	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #63	C[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C)[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@H](CO[C@@H]2O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)[C@H]1O	4995.2	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #64	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)[C@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)O[C@H]1O	4997.8	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #65	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4994.3	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #66	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4977.3	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #67	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4951.1	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #68	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4987.6	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #69	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3O[Si](C)(C)C)C2)C=C1O	4933.7	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #7	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3O[Si](C)(C)C)C2)C=C1O	4983.7	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #70	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3O[Si](C)(C)C)C2)=CC=C1O	4952.9	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #71	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)C=C1O	4944.6	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #72	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C=C3C2)C=C1O	4922.3	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #73	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3C2)C=C1O	4884.9	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #74	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3C2)C=C1O	4915.5	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #75	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)C=C1O[Si](C)(C)C	4995.1	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #76	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)=CC=C1O	4954.8	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #77	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C=C3C2)=CC=C1O	4929.5	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #78	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3C2)=CC=C1O	4900.0	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #79	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3C2)=CC=C1O	4928.4	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #8	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3O[Si](C)(C)C)C2)=CC=C1O	5003.6	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #80	C[Si](C)(C)O[C@H]1[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@H](CO[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H](O)[C@@H]1O	5013.5	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #81	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@@H]1CO[C@@H]1O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O	4992.9	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #82	C[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C)[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@H](CO[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)[C@H]1O	4977.5	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #83	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@H](CO[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@H]1O	4974.0	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #84	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](O)O[C@@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H]1O	4980.6	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #85	C[Si](C)(C)O[C@@H]1[C@@H](CO[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[C@@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)[C@H](O)[C@H]1O	5007.1	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #86	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4987.9	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #87	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4967.8	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #88	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4998.1	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #89	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]4O)C=C3O[Si](C)(C)C)C2)C=C1O	4952.5	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #9	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)C=C1O	4979.5	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #90	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]4O)C=C3O[Si](C)(C)C)C2)=CC=C1O	4971.6	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #91	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C=C3C2)C=C1O	4934.9	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #92	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3C2)C=C1O	4898.4	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #93	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3C2)C=C1O	4934.8	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #94	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)C=C1O[Si](C)(C)C	5011.5	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #95	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C=C3C2)=CC=C1O	4938.8	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #96	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3C2)=CC=C1O	4911.6	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #97	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3C2)=CC=C1O	4941.7	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #98	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@@H]1CO[C@@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C	5006.7	Semi standard non polar	33892256
Eriocitrin,3TMS,isomer #99	C[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C)[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@H](CO[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@H]1O	4993.8	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #1	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O)[C@@H](O)[C@H](O)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4891.7	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #10	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4844.9	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #100	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C=C3C2)=CC=C1O	4841.9	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #101	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3C2)=CC=C1O	4808.3	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #102	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3C2)=CC=C1O	4842.0	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #103	C[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C)[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@H](CO[C@@H]2O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O)[C@H]1O	4901.5	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #104	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@@H]1CO[C@@H]1O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O	4915.7	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #105	C[Si](C)(C)O[C@H]1[C@@H](O)[C@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)O[C@@H](O)[C@@H]1O[Si](C)(C)C	4900.3	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #106	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4914.5	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #107	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4880.6	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #108	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4926.2	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #109	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]4O)C=C3O[Si](C)(C)C)C2)C=C1O	4835.7	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #11	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4886.7	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #110	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]4O)C=C3O[Si](C)(C)C)C2)=CC=C1O	4864.5	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #111	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C=C3C2)C=C1O	4833.2	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #112	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3C2)C=C1O	4804.6	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #113	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3C2)C=C1O	4831.5	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #114	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)C=C1O[Si](C)(C)C	4898.7	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #115	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C=C3C2)=CC=C1O	4849.0	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #116	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3C2)=CC=C1O	4819.0	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #117	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3C2)=CC=C1O	4848.6	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #118	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@@H]1CO[C@@H]1O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C	4927.1	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #119	C[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C)[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@H](CO[C@@H]2O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@H]1O	4912.7	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #12	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3O[Si](C)(C)C)C2)C=C1O	4833.2	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #120	C[Si](C)(C)O[C@H]1[C@H](O)O[C@@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O	4910.6	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #121	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4906.8	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #122	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4922.0	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #123	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C=C3O[Si](C)(C)C)C2)C=C1O	4841.1	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #124	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C=C3O[Si](C)(C)C)C2)=CC=C1O	4869.9	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #125	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4914.1	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #126	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3O[Si](C)(C)C)C2)C=C1O	4819.4	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #127	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3O[Si](C)(C)C)C2)=CC=C1O	4846.3	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #128	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3O[Si](C)(C)C)C2)C=C1O	4838.3	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #129	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3O[Si](C)(C)C)C2)=CC=C1O	4866.3	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #13	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3O[Si](C)(C)C)C2)=CC=C1O	4862.6	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #130	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3O[Si](C)(C)C)C2)C=C1O[Si](C)(C)C	4904.9	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #131	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3C2)C=C1O	4835.1	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #132	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3C2)C=C1O	4842.8	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #133	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C=C3C2)C=C1O[Si](C)(C)C	4901.8	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #134	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C=C3C2)C=C1O	4828.9	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #135	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3C2)C=C1O[Si](C)(C)C	4876.2	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #136	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3C2)C=C1O[Si](C)(C)C	4903.2	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #137	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3C2)=CC=C1O	4853.0	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #138	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3C2)=CC=C1O	4857.6	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #139	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C=C3C2)=CC=C1O	4847.9	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #14	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4892.4	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #140	C[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C)[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@H](CO[C@@H]2O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)[C@H]1O[Si](C)(C)C	4948.3	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #141	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4920.4	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #142	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4886.0	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #143	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4931.5	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #144	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]4O)C=C3O[Si](C)(C)C)C2)C=C1O	4841.2	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #145	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]4O)C=C3O[Si](C)(C)C)C2)=CC=C1O	4871.5	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #146	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4887.3	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #147	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4901.8	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #148	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C=C3O[Si](C)(C)C)C2)C=C1O	4822.1	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #149	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C=C3O[Si](C)(C)C)C2)=CC=C1O	4851.1	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #15	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4857.9	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #150	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4894.1	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #151	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3O[Si](C)(C)C)C2)C=C1O	4800.2	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #152	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3O[Si](C)(C)C)C2)=CC=C1O	4826.2	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #153	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3O[Si](C)(C)C)C2)C=C1O	4821.3	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #154	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3O[Si](C)(C)C)C2)=CC=C1O	4850.0	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #155	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3O[Si](C)(C)C)C2)C=C1O[Si](C)(C)C	4886.1	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #156	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C=C3C2)C=C1O	4837.5	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #157	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3C2)C=C1O	4804.5	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #158	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3C2)C=C1O	4838.6	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #159	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)C=C1O[Si](C)(C)C	4910.4	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #16	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4898.2	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #160	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3C2)C=C1O	4817.0	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #161	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3C2)C=C1O	4824.9	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #162	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C=C3C2)C=C1O[Si](C)(C)C	4884.2	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #163	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C=C3C2)C=C1O	4811.6	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #164	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3C2)C=C1O[Si](C)(C)C	4859.8	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #165	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3C2)C=C1O[Si](C)(C)C	4886.2	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #166	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C=C3C2)=CC=C1O	4858.4	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #167	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3C2)=CC=C1O	4823.0	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #168	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3C2)=CC=C1O	4859.5	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #169	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3C2)=CC=C1O	4836.9	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #17	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]4O)C=C3O[Si](C)(C)C)C2)C=C1O	4844.8	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #170	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3C2)=CC=C1O	4842.3	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #171	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C=C3C2)=CC=C1O	4831.9	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #172	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@@H]1CO[C@@H]1O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4933.9	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #173	C[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C)[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@H](CO[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@H]1O	4921.6	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #174	C[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C)[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@H](CO[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)[C@H]1O[Si](C)(C)C	4929.5	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #175	C[Si](C)(C)O[C@@H]1[C@@H](CO[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[C@@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)[C@H](O)[C@H]1O[Si](C)(C)C	4920.5	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #176	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4915.5	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #177	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4926.4	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #178	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C=C3O[Si](C)(C)C)C2)C=C1O	4838.3	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #179	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C=C3O[Si](C)(C)C)C2)=CC=C1O	4865.8	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #18	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]4O)C=C3O[Si](C)(C)C)C2)=CC=C1O	4874.9	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #180	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4923.7	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #181	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3O[Si](C)(C)C)C2)C=C1O	4816.5	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #182	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3O[Si](C)(C)C)C2)=CC=C1O	4843.6	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #183	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3O[Si](C)(C)C)C2)C=C1O	4840.6	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #184	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3O[Si](C)(C)C)C2)=CC=C1O	4872.1	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #185	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]4O)C=C3O[Si](C)(C)C)C2)C=C1O[Si](C)(C)C	4905.3	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #186	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3C2)C=C1O	4834.9	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #187	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3C2)C=C1O	4841.9	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #188	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C=C3C2)C=C1O[Si](C)(C)C	4900.7	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #189	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C=C3C2)C=C1O	4831.0	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #19	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]3O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4884.9	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #190	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3C2)C=C1O[Si](C)(C)C	4875.0	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #191	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3C2)C=C1O[Si](C)(C)C	4904.9	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #192	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3C2)=CC=C1O	4857.0	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #193	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3C2)=CC=C1O	4860.7	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #194	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C=C3C2)=CC=C1O	4853.2	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #195	C[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C)[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@H](CO[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4949.1	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #196	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O)[C@@H](O)[C@H]3O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4948.6	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #197	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3O[Si](C)(C)C)C2)C=C1O	4850.3	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #198	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3O[Si](C)(C)C)C2)=CC=C1O	4878.7	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #199	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3O[Si](C)(C)C)C2)C=C1O	4850.6	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #2	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4892.3	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #20	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]3O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4896.2	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #200	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3O[Si](C)(C)C)C2)=CC=C1O	4876.8	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #201	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C=C3O[Si](C)(C)C)C2)C=C1O[Si](C)(C)C	4909.4	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #202	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C=C3C2)C=C1O	4890.5	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #203	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3C2)C=C1O[Si](C)(C)C	4915.4	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #204	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3C2)C=C1O[Si](C)(C)C	4918.5	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #205	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C=C3C2)=CC=C1O	4912.1	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #206	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C=C3O[Si](C)(C)C)C2)C=C1O	4845.5	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #207	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C=C3O[Si](C)(C)C)C2)=CC=C1O	4875.6	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #208	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C=C3C2)C=C1O[Si](C)(C)C	4913.3	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #209	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3O[Si](C)(C)C)C2)C=C1O[Si](C)(C)C	4887.0	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #21	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C=C3O[Si](C)(C)C)C2)C=C1O	4849.2	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #210	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3O[Si](C)(C)C)C2)C=C1O[Si](C)(C)C	4911.5	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #22	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C=C3O[Si](C)(C)C)C2)=CC=C1O	4877.8	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #23	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]3O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4889.6	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #24	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3O[Si](C)(C)C)C2)C=C1O	4827.2	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #25	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3O[Si](C)(C)C)C2)=CC=C1O	4853.0	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #26	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3O[Si](C)(C)C)C2)C=C1O	4845.0	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #27	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3O[Si](C)(C)C)C2)=CC=C1O	4873.2	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #28	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3O[Si](C)(C)C)C2)C=C1O[Si](C)(C)C	4909.4	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #29	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)C=C1O	4859.4	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #3	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4902.3	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #30	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)C=C1O	4853.8	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #31	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C=C3C2)C=C1O	4858.3	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #32	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3C2)C=C1O	4826.7	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #33	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3C2)C=C1O	4855.5	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #34	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)C=C1O[Si](C)(C)C	4922.8	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #35	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)C=C1O	4855.0	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #36	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C=C3C2)C=C1O	4840.1	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #37	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3C2)C=C1O	4812.4	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #38	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3C2)C=C1O	4836.1	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #39	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)C=C1O[Si](C)(C)C	4898.4	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #4	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4869.0	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #40	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C=C3C2)C=C1O	4849.3	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #41	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3C2)C=C1O	4818.3	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #42	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3C2)C=C1O	4845.4	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #43	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)C=C1O[Si](C)(C)C	4911.1	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #44	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3C2)C=C1O	4852.1	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #45	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3C2)C=C1O	4858.8	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #46	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C=C3C2)C=C1O[Si](C)(C)C	4914.6	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #47	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C=C3C2)C=C1O	4845.0	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #48	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3C2)C=C1O[Si](C)(C)C	4888.0	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #49	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3C2)C=C1O[Si](C)(C)C	4912.8	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #5	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4905.6	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #50	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)=CC=C1O	4878.5	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #51	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)=CC=C1O	4875.8	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #52	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C=C3C2)=CC=C1O	4875.7	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #53	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3C2)=CC=C1O	4841.0	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #54	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3C2)=CC=C1O	4873.0	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #55	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)=CC=C1O	4877.3	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #56	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C=C3C2)=CC=C1O	4855.3	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #57	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3C2)=CC=C1O	4826.1	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #58	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3C2)=CC=C1O	4851.8	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #59	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C=C3C2)=CC=C1O	4867.1	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #6	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3O[Si](C)(C)C)C2)C=C1O	4851.2	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #60	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3C2)=CC=C1O	4834.6	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #61	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3C2)=CC=C1O	4864.7	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #62	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3C2)=CC=C1O	4872.4	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #63	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3C2)=CC=C1O	4875.9	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #64	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C=C3C2)=CC=C1O	4866.7	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #65	C[Si](C)(C)O[C@@H]1O[C@@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4924.3	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #66	C[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C)[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@H](CO[C@@H]2O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@H]1O	4889.0	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #67	C[Si](C)(C)O[C@@H]1O[C@@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4880.3	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #68	C[Si](C)(C)O[C@@H]1O[C@@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4902.2	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #69	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@@H]1CO[C@@H]1O[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O	4918.1	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #7	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3O[Si](C)(C)C)C2)=CC=C1O	4880.1	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #70	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@@H]1CO[C@@H]1O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O	4896.7	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #71	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@@H]1CO[C@@H]1O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C	4902.4	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #72	C[Si](C)(C)O[C@@H]1O[C@@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4905.6	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #73	C[Si](C)(C)O[C@@H]1O[C@@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4908.7	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #74	C[Si](C)(C)O[C@@H]1O[C@@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4907.6	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #75	C[Si](C)(C)O[C@@H]1O[C@@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4889.0	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #76	C[Si](C)(C)O[C@@H]1O[C@@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4880.5	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #77	C[Si](C)(C)O[C@@H]1O[C@@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4904.2	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #78	C[Si](C)(C)O[C@@H]1O[C@@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4864.9	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #79	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@H](CO[C@@H]2O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@H]1O	4860.3	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #8	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4892.5	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #80	C[Si](C)(C)O[C@@H]1O[C@@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4863.5	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #81	C[Si](C)(C)O[C@@H]1O[C@@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4905.4	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #82	C[Si](C)(C)O[C@@H]1[C@@H](CO[C@@H]2O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[C@@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)[C@H](O)[C@H]1O	4902.6	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #83	C[Si](C)(C)O[C@@H]1O[C@@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4905.5	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #84	C[Si](C)(C)O[C@@H]1O[C@@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4913.2	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #85	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4929.5	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #86	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)C=C1O	4850.3	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #87	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]5O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)=CC=C1O	4875.6	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #88	C[Si](C)(C)O[C@H]1[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@H](CO[C@@H]2O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4941.3	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #89	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@H](CO[C@@H]2O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@H]1O	4891.4	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #9	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4880.9	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #90	C[Si](C)(C)O[C@@H]1[C@@H](CO[C@@H]2O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[C@@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)[C@H](O)[C@H]1O	4934.7	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #91	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4899.6	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #92	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4861.5	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #93	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	4908.3	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #94	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3O[Si](C)(C)C)C2)C=C1O	4826.8	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #95	C[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3O[Si](C)(C)C)C2)=CC=C1O	4856.0	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #96	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C=C3C2)C=C1O	4823.0	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #97	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3C2)C=C1O	4792.6	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #98	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3C2)C=C1O	4823.6	Semi standard non polar	33892256
Eriocitrin,4TMS,isomer #99	C[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)C=C1O[Si](C)(C)C	4895.9	Semi standard non polar	33892256
Eriocitrin,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)O[C@@H]1O[C@@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5415.0	Semi standard non polar	33892256
Eriocitrin,1TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)=CC=C1O	5437.7	Semi standard non polar	33892256
Eriocitrin,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)[C@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O)[C@@H](O)[C@@H]2O)O[C@H]1O	5424.6	Semi standard non polar	33892256
Eriocitrin,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](O)O[C@@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O)[C@@H](O)[C@@H]2O)[C@@H]1O	5401.7	Semi standard non polar	33892256
Eriocitrin,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O)[C@@H](O)[C@@H]2O)O[C@@H](O)[C@H](O)[C@H]1O	5414.8	Semi standard non polar	33892256
Eriocitrin,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O)O[C@@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)[C@H](O)[C@H]1O	5431.8	Semi standard non polar	33892256
Eriocitrin,1TBDMS,isomer #6	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@H](CO[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O)[C@H]1O	5404.6	Semi standard non polar	33892256
Eriocitrin,1TBDMS,isomer #7	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@H](CO[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O)[C@@H](O)[C@@H]1O	5422.6	Semi standard non polar	33892256
Eriocitrin,1TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O)[C@@H](O)[C@H]3O)[C@@H](O)[C@H](O)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	5408.7	Semi standard non polar	33892256
Eriocitrin,1TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)C=C1O	5439.1	Semi standard non polar	33892256
Eriocitrin,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@H]3O)[C@@H](O)[C@H](O)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	5449.3	Semi standard non polar	33892256
Eriocitrin,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)[C@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O)[C@@H](O)[C@@H]2O)O[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	5448.0	Semi standard non polar	33892256
Eriocitrin,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)O[C@@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	5464.3	Semi standard non polar	33892256
Eriocitrin,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]3O)[C@@H](O)[C@H](O)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	5466.4	Semi standard non polar	33892256
Eriocitrin,2TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)C=C1O	5516.2	Semi standard non polar	33892256
Eriocitrin,2TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)=CC=C1O	5519.0	Semi standard non polar	33892256
Eriocitrin,2TBDMS,isomer #15	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@H](CO[C@@H]2O[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O)[C@@H](O)[C@@H]1O	5474.8	Semi standard non polar	33892256
Eriocitrin,2TBDMS,isomer #16	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@H](CO[C@@H]2O[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O)[C@H]1O	5454.1	Semi standard non polar	33892256
Eriocitrin,2TBDMS,isomer #17	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO[C@@H]2O[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O)O[C@@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)[C@H](O)[C@H]1O	5476.4	Semi standard non polar	33892256
Eriocitrin,2TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)[C@@H](O)[C@H](O)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	5435.8	Semi standard non polar	33892256
Eriocitrin,2TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)C=C1O	5476.8	Semi standard non polar	33892256
Eriocitrin,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)C=C1O	5502.2	Semi standard non polar	33892256
Eriocitrin,2TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)=CC=C1O	5485.8	Semi standard non polar	33892256
Eriocitrin,2TBDMS,isomer #21	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@H](CO[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H](O)[C@@H]1O	5451.5	Semi standard non polar	33892256
Eriocitrin,2TBDMS,isomer #22	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@H](CO[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@H]1O	5429.2	Semi standard non polar	33892256
Eriocitrin,2TBDMS,isomer #23	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)O[C@@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)[C@H](O)[C@H]1O	5451.8	Semi standard non polar	33892256
Eriocitrin,2TBDMS,isomer #24	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O)[C@@H](O)[C@@H]2O)O[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	5460.4	Semi standard non polar	33892256
Eriocitrin,2TBDMS,isomer #25	CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	5450.1	Semi standard non polar	33892256
Eriocitrin,2TBDMS,isomer #26	CC(C)(C)[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)C=C1O	5483.2	Semi standard non polar	33892256
Eriocitrin,2TBDMS,isomer #27	CC(C)(C)[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)=CC=C1O	5490.7	Semi standard non polar	33892256
Eriocitrin,2TBDMS,isomer #28	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@H](CO[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	5464.5	Semi standard non polar	33892256
Eriocitrin,2TBDMS,isomer #29	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@H](CO[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H]1O	5442.3	Semi standard non polar	33892256
Eriocitrin,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)=CC=C1O	5507.6	Semi standard non polar	33892256
Eriocitrin,2TBDMS,isomer #30	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)O[C@@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)[C@H](O)[C@H]1O	5463.8	Semi standard non polar	33892256
Eriocitrin,2TBDMS,isomer #31	CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O)[C@@H](O)[C@H]3O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	5461.5	Semi standard non polar	33892256
Eriocitrin,2TBDMS,isomer #32	CC(C)(C)[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]4O)C=C3C2)C=C1O	5501.4	Semi standard non polar	33892256
Eriocitrin,2TBDMS,isomer #33	CC(C)(C)[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]4O)C=C3C2)=CC=C1O	5506.2	Semi standard non polar	33892256
Eriocitrin,2TBDMS,isomer #34	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@@H]1CO[C@@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@H]1O	5471.2	Semi standard non polar	33892256
Eriocitrin,2TBDMS,isomer #35	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O)O[C@@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	5461.3	Semi standard non polar	33892256
Eriocitrin,2TBDMS,isomer #36	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](OC2=CC(O)=C3C(=O)C[C@@H](C4=CC=C(O)C(O)=C4)CC3=C2)O[C@H](CO[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O)[C@H]1O	5459.9	Semi standard non polar	33892256
Eriocitrin,2TBDMS,isomer #37	CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O)[C@@H](O)[C@H]3O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	5436.5	Semi standard non polar	33892256
Eriocitrin,2TBDMS,isomer #38	CC(C)(C)[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O)C=C3C2)C=C1O	5473.1	Semi standard non polar	33892256
Eriocitrin,2TBDMS,isomer #39	CC(C)(C)[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O)C=C3C2)=CC=C1O	5479.0	Semi standard non polar	33892256
Eriocitrin,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@@H]1O[C@@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5463.8	Semi standard non polar	33892256
Eriocitrin,2TBDMS,isomer #40	CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](O)[C@H](O)[C@@H](O)[C@H]3O)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)=CC2=C1C(=O)C[C@@H](C1=CC=C(O)C(O)=C1)C2	5457.6	Semi standard non polar	33892256
Eriocitrin,2TBDMS,isomer #41	CC(C)(C)[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)C=C3C2)C=C1O	5490.0	Semi standard non polar	33892256
Eriocitrin,2TBDMS,isomer #42	CC(C)(C)[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)C=C3C2)=CC=C1O	5494.9	Semi standard non polar	33892256
Eriocitrin,2TBDMS,isomer #43	CC(C)(C)[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3O[Si](C)(C)C(C)(C)C)C2)C=C1O	5490.7	Semi standard non polar	33892256
Eriocitrin,2TBDMS,isomer #44	CC(C)(C)[Si](C)(C)OC1=CC([C@@H]2CC(=O)C3=C(C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3O[Si](C)(C)C(C)(C)C)C2)=CC=C1O	5504.1	Semi standard non polar	33892256
Eriocitrin,2TBDMS,isomer #45	CC(C)(C)[Si](C)(C)OC1=CC=C([C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](O)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3C2)C=C1O[Si](C)(C)C(C)(C)C	5530.6	Semi standard non polar	33892256
Eriocitrin,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)O[C@@H]1O[C@@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5441.5	Semi standard non polar	33892256
Eriocitrin,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)O[C@@H]1O[C@@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O)[C@@H](O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5464.6	Semi standard non polar	33892256
Eriocitrin,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)O[C@@H]1O[C@@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	5458.8	Semi standard non polar	33892256
Eriocitrin,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)O[C@@H]1O[C@@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	5456.7	Semi standard non polar	33892256
Eriocitrin,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)O[C@@H]1O[C@@H](OC[C@H]2O[C@@H](OC3=CC(O)=C4C(=O)C[C@@H](C5=CC=C(O)C(O)=C5)CC4=C3)[C@H](O)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	5461.7	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 - Eriocitrin GC-MS (Non-derivatized) - 70eV, Positive	splash10-004i-1231190000-505f1d9bb7f242fb987e	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eriocitrin GC-MS (1 TMS) - 70eV, Positive	splash10-0ufr-2221029000-04763105bd7630d30bf2	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eriocitrin GC-MS ("Eriocitrin,1TMS,#1" TMS) - 70eV, Positive	Not Available	2021-10-14	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eriocitrin GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eriocitrin GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eriocitrin GC-MS (TMS_1_4) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eriocitrin GC-MS (TMS_1_5) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eriocitrin GC-MS (TMS_1_6) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eriocitrin GC-MS (TMS_1_7) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eriocitrin GC-MS (TMS_1_8) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eriocitrin GC-MS (TMS_1_9) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eriocitrin GC-MS (TMS_1_10) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eriocitrin GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eriocitrin GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eriocitrin GC-MS (TMS_2_3) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eriocitrin GC-MS (TMS_2_4) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eriocitrin GC-MS (TMS_2_5) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eriocitrin GC-MS (TMS_2_6) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eriocitrin GC-MS (TMS_2_7) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eriocitrin GC-MS (TMS_2_8) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eriocitrin GC-MS (TMS_2_9) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eriocitrin GC-MS (TMS_2_10) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eriocitrin GC-MS (TMS_2_11) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eriocitrin GC-MS (TMS_2_12) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eriocitrin GC-MS (TMS_2_13) - 70eV, Positive	Not Available	2021-10-16	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 - Eriocitrin 10V, Positive-QTOF	splash10-002r-0190170000-e9b31979680d327e54a6	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Eriocitrin 20V, Positive-QTOF	splash10-000i-0490100000-34b891aac7d68bc3dace	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Eriocitrin 40V, Positive-QTOF	splash10-000i-1590000000-70ebeb272bc4a9389e81	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Eriocitrin 10V, Negative-QTOF	splash10-000b-1350290000-049d54623673010dce39	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Eriocitrin 20V, Negative-QTOF	splash10-000i-2490020000-0769c6fe6e8f9dbe1bed	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Eriocitrin 40V, Negative-QTOF	splash10-000i-2190000000-b4960ba583e1eef025ce	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Eriocitrin 10V, Negative-QTOF	splash10-000i-0090270000-d276d91f318ad83fb740	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Eriocitrin 20V, Negative-QTOF	splash10-000i-1290110000-2a29e0a98ff3df1bd444	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Eriocitrin 40V, Negative-QTOF	splash10-05n0-1290000000-f1d331c5abe81c6ba41a	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Eriocitrin 10V, Positive-QTOF	splash10-002s-0180390000-c6bdc10f18f7897b770c	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Eriocitrin 20V, Positive-QTOF	splash10-014r-0290230000-b8222c1f9b84d9888802	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Eriocitrin 40V, Positive-QTOF	splash10-01qi-3246910000-b9ccc612acc1b89bb69d	2021-09-24	Wishart Lab	View Spectrum

NMR Spectra

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

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

KNApSAcK ID

Chemspider ID

KEGG Compound ID

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Eriocitrin

METLIN ID

Not Available

PubChem Compound

22833655

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

rw1700811

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Download (PDF)

General References

Not Available

Showing metabocard for Eriocitrin (HMDB0005811)

MOL for HMDB0005811 (Eriocitrin)

3D MOL for HMDB0005811 (Eriocitrin)

3D SDF for HMDB0005811 (Eriocitrin)

3D-SDF for HMDB0005811 (Eriocitrin)

PDB for HMDB0005811 (Eriocitrin)

3D PDB for HMDB0005811 (Eriocitrin)

SMILES for HMDB0005811 (Eriocitrin)

INCHI for HMDB0005811 (Eriocitrin)

Structure for HMDB0005811 (Eriocitrin)

3D Structure for HMDB0005811 (Eriocitrin)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra