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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-12 01:27:51 UTC

Update Date

2022-03-07 02:56:24 UTC

HMDB ID

HMDB0039921

Secondary Accession Numbers

HMDB39921

Metabolite Identification

Common Name

Eriodictyol 7-(6-galloylglucoside)

Description

Eriodictyol 7-(6-galloylglucoside) belongs to the class of organic compounds known as flavonoid-7-o-glycosides. These are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C7-position. Eriodictyol 7-(6-galloylglucoside) has been detected, but not quantified in, fruits. This could make eriodictyol 7-(6-galloylglucoside) a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on Eriodictyol 7-(6-galloylglucoside).

Structure

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


  Mrv0541 05061311302D          

 43 47  0  0  0  0            999 V2000
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    5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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 43 21  1  0  0  0  0
 43 28  1  0  0  0  0
M  END

HMDB0039921
     RDKit          3D
Eriodictyol 7-(6-galloylglucoside)
 69 73  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv0541 05061311302D          

 43 47  0  0  0  0            999 V2000
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   -2.1434   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  2  0  0  0  0
 10  1  1  0  0  0  0
 10  3  2  0  0  0  0
 11  4  2  0  0  0  0
 11  5  1  0  0  0  0
 12  6  2  0  0  0  0
 12  7  1  0  0  0  0
 13  2  1  0  0  0  0
 14  3  1  0  0  0  0
 14 13  2  0  0  0  0
 15  6  1  0  0  0  0
 16  8  1  0  0  0  0
 17  4  1  0  0  0  0
 18  5  2  0  0  0  0
 19  8  1  0  0  0  0
 19 10  1  0  0  0  0
 20  7  2  0  0  0  0
 21  9  1  0  0  0  0
 22 15  2  0  0  0  0
 22 16  1  0  0  0  0
 22 20  1  0  0  0  0
 23 17  2  0  0  0  0
 23 18  1  0  0  0  0
 24 21  1  0  0  0  0
 25 24  1  0  0  0  0
 26 25  1  0  0  0  0
 27 11  1  0  0  0  0
 28 26  1  0  0  0  0
 29 13  1  0  0  0  0
 30 14  1  0  0  0  0
 31 15  1  0  0  0  0
 32 16  2  0  0  0  0
 33 17  1  0  0  0  0
 34 18  1  0  0  0  0
 35 23  1  0  0  0  0
 36 24  1  0  0  0  0
 37 25  1  0  0  0  0
 38 26  1  0  0  0  0
 39 27  2  0  0  0  0
 40  9  1  0  0  0  0
 40 27  1  0  0  0  0
 41 12  1  0  0  0  0
 41 28  1  0  0  0  0
 42 19  1  0  0  0  0
 42 20  1  0  0  0  0
 43 21  1  0  0  0  0
 43 28  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0039921

> <DATABASE_NAME>
hmdb

> <SMILES>
OC1C(O)C(COC(=O)C2=CC(O)=C(O)C(O)=C2)OC(OC2=CC(O)=C3C(=O)CC(OC3=C2)C2=CC(O)=C(O)C=C2)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C28H26O15/c29-13-2-1-10(3-14(13)30)19-8-16(32)22-15(31)6-12(7-20(22)42-19)41-28-26(38)25(37)24(36)21(43-28)9-40-27(39)11-4-17(33)23(35)18(34)5-11/h1-7,19,21,24-26,28-31,33-38H,8-9H2

> <INCHI_KEY>
SHPCBRSOJXQRDY-UHFFFAOYSA-N

> <FORMULA>
C28H26O15

> <MOLECULAR_WEIGHT>
602.497

> <EXACT_MASS>
602.127170162

> <JCHEM_ACCEPTOR_COUNT>
14

> <JCHEM_AVERAGE_POLARIZABILITY>
56.664445154548716

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
9

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(6-{[2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-3,4-dihydro-2H-1-benzopyran-7-yl]oxy}-3,4,5-trihydroxyoxan-2-yl)methyl 3,4,5-trihydroxybenzoate

> <ALOGPS_LOGP>
1.50

> <JCHEM_LOGP>
1.848078519

> <ALOGPS_LOGS>
-3.09

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.150861256869463

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.067591811780655

> <JCHEM_PKA_STRONGEST_BASIC>
-3.678965823839513

> <JCHEM_POLAR_SURFACE_AREA>
253.1299999999999

> <JCHEM_REFRACTIVITY>
141.1798

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.92e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(6-{[2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-2,3-dihydro-1-benzopyran-7-yl]oxy}-3,4,5-trihydroxyoxan-2-yl)methyl 3,4,5-trihydroxybenzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0039921
     RDKit          3D
Eriodictyol 7-(6-galloylglucoside)
 69 73  0  0  0  0  0  0  0  0999 V2000
    5.5839    1.1612   -2.8868 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5871    0.8065   -1.6832 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3650    0.6844   -1.0630 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1316    0.9350   -1.7058 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9550    0.7242   -0.7912 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0045   -0.6193   -0.3753 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1507   -0.8457    0.7116 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1077   -0.2968    0.5345 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2941   -0.9759    0.4734 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4342   -2.3373    0.5795 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6752   -2.9827    0.5098 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7837   -4.3616    0.6207 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7965   -2.2339    0.3289 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7108   -0.8607    0.2162 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4827   -0.2431    0.2871 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8848   -0.1020    0.0292 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9782   -0.7539   -0.5474 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1416    0.1481   -0.7262 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8251    0.1081   -1.9221 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9188    0.8941   -2.2089 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3152    1.7593   -1.2021 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4022    2.5835   -1.4045 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6529    1.8168   -0.0074 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0940    2.7110    0.9816 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5616    1.0196    0.2539 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3050   -1.9426    0.3328 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1379   -2.8568    0.2471 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2361   -4.0940    0.1127 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8763   -0.2694    1.9188 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9009   -1.1543    2.2376 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5066    1.0614    1.6046 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2261    1.9268    2.6607 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8844    1.6754    0.3433 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5277    2.8805    0.1287 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8574    0.5511   -1.0296 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0205    0.7029   -1.7399 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2702    0.4701   -1.1592 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4509    0.6214   -1.8709 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.3691    0.0771    0.1582 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6078   -0.1616    0.7611 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.2125   -0.0772    0.8761 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2602   -0.4672    2.1922 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9671    0.1589    0.2837 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1209    1.9693   -2.1080 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0836    0.2625   -2.5859 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0208    0.8135   -1.3833 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0785   -1.9419    0.8005 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5647   -2.9696    0.7242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9601   -4.9415    0.7561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4224    0.8416    0.1973 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6716   -1.1241   -1.5359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5018   -0.5823   -2.7141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4525    0.8585   -3.1510 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.9330    2.5790   -2.2824 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6497    2.7939    1.8679 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0222    1.0461    1.1879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3122   -1.5607    1.3935 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2439   -2.4408    0.0577 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1268   -0.1629    2.7241 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5666   -2.0451    2.5035 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6108    0.9617    1.4545 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0962    1.4586    3.5190 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8289    1.9237    0.6460 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1066    3.1445    0.8745 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0099    1.0089   -2.7772 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.4481    0.9109   -2.8534 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.4586   -0.0458    0.2251 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1541   -0.6391    2.6260 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0464    0.0394    0.8438 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  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 11 13  2  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 23 25  2  0
 17 26  1  0
 26 27  1  0
 27 28  2  0
  7 29  1  0
 29 30  1  0
 29 31  1  0
 31 32  1  0
 31 33  1  0
 33 34  1  0
  2 35  1  0
 35 36  2  0
 36 37  1  0
 37 38  1  0
 37 39  2  0
 39 40  1  0
 39 41  1  0
 41 42  1  0
 41 43  2  0
 33  5  1  0
 43 35  1  0
 15  9  1  0
 25 18  1  0
 27 13  1  0
  4 44  1  0
  4 45  1  0
  5 46  1  0
  7 47  1  0
 10 48  1  0
 12 49  1  0
 15 50  1  0
 17 51  1  0
 19 52  1  0
 20 53  1  0
 22 54  1  0
 24 55  1  0
 25 56  1  0
 26 57  1  0
 26 58  1  0
 29 59  1  0
 30 60  1  0
 31 61  1  0
 32 62  1  0
 33 63  1  0
 34 64  1  0
 36 65  1  0
 38 66  1  0
 40 67  1  0
 42 68  1  0
 43 69  1  0
M  END

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0       9.336  -2.310   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.669  -3.080   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      10.669   0.000   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -6.668  -5.390   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -5.335  -3.080   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.336  -0.770   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      12.003  -2.310   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      12.003  -0.770   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -8.002  -4.620   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.002   0.000   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -8.002  -3.080   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      13.337  -3.080   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      13.337   0.000   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       4.001   3.850   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       6.668   3.850   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0      -9.336  -5.390   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0      -6.668  -0.770   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0      -9.336  -2.310   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0       1.334  -6.930   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0       4.001  -5.390   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0       4.001  -2.310   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0      -4.001  -6.930   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0      -2.667  -4.620   0.000  0.00  0.00           O+0
HETATM   41  O   UNK     0       1.334  -0.770   0.000  0.00  0.00           O+0
HETATM   42  O   UNK     0       6.668  -0.770   0.000  0.00  0.00           O+0
HETATM   43  O   UNK     0       0.000  -3.080   0.000  0.00  0.00           O+0
CONECT    1    2   10                                                       
CONECT    2    1   13                                                       
CONECT    3   10   14                                                       
CONECT    4   11   17                                                       
CONECT    5   11   18                                                       
CONECT    6   12   15                                                       
CONECT    7   12   20                                                       
CONECT    8   16   19                                                       
CONECT    9   21   40                                                       
CONECT   10    1    3   19                                                  
CONECT   11    4    5   27                                                  
CONECT   12    6    7   41                                                  
CONECT   13    2   14   29                                                  
CONECT   14    3   13   30                                                  
CONECT   15    6   22   31                                                  
CONECT   16    8   22   32                                                  
CONECT   17    4   23   33                                                  
CONECT   18    5   23   34                                                  
CONECT   19    8   10   42                                                  
CONECT   20    7   22   42                                                  
CONECT   21    9   24   43                                                  
CONECT   22   15   16   20                                                  
CONECT   23   17   18   35                                                  
CONECT   24   21   25   36                                                  
CONECT   25   24   26   37                                                  
CONECT   26   25   28   38                                                  
CONECT   27   11   39   40                                                  
CONECT   28   26   41   43                                                  
CONECT   29   13                                                            
CONECT   30   14                                                            
CONECT   31   15                                                            
CONECT   32   16                                                            
CONECT   33   17                                                            
CONECT   34   18                                                            
CONECT   35   23                                                            
CONECT   36   24                                                            
CONECT   37   25                                                            
CONECT   38   26                                                            
CONECT   39   27                                                            
CONECT   40    9   27                                                       
CONECT   41   12   28                                                       
CONECT   42   19   20                                                       
CONECT   43   21   28                                                       
MASTER        0    0    0    0    0    0    0    0   43    0   94    0
END

COMPND    HMDB0039921
HETATM    1  O1  UNL     1       5.584   1.161  -2.887  1.00  0.00           O  
HETATM    2  C1  UNL     1       5.587   0.807  -1.683  1.00  0.00           C  
HETATM    3  O2  UNL     1       4.365   0.684  -1.063  1.00  0.00           O  
HETATM    4  C2  UNL     1       3.132   0.935  -1.706  1.00  0.00           C  
HETATM    5  C3  UNL     1       1.955   0.724  -0.791  1.00  0.00           C  
HETATM    6  O3  UNL     1       2.004  -0.619  -0.375  1.00  0.00           O  
HETATM    7  C4  UNL     1       1.151  -0.846   0.712  1.00  0.00           C  
HETATM    8  O4  UNL     1      -0.108  -0.297   0.535  1.00  0.00           O  
HETATM    9  C5  UNL     1      -1.294  -0.976   0.473  1.00  0.00           C  
HETATM   10  C6  UNL     1      -1.434  -2.337   0.579  1.00  0.00           C  
HETATM   11  C7  UNL     1      -2.675  -2.983   0.510  1.00  0.00           C  
HETATM   12  O5  UNL     1      -2.784  -4.362   0.621  1.00  0.00           O  
HETATM   13  C8  UNL     1      -3.797  -2.234   0.329  1.00  0.00           C  
HETATM   14  C9  UNL     1      -3.711  -0.861   0.216  1.00  0.00           C  
HETATM   15  C10 UNL     1      -2.483  -0.243   0.287  1.00  0.00           C  
HETATM   16  O6  UNL     1      -4.885  -0.102   0.029  1.00  0.00           O  
HETATM   17  C11 UNL     1      -5.978  -0.754  -0.547  1.00  0.00           C  
HETATM   18  C12 UNL     1      -7.142   0.148  -0.726  1.00  0.00           C  
HETATM   19  C13 UNL     1      -7.825   0.108  -1.922  1.00  0.00           C  
HETATM   20  C14 UNL     1      -8.919   0.894  -2.209  1.00  0.00           C  
HETATM   21  C15 UNL     1      -9.315   1.759  -1.202  1.00  0.00           C  
HETATM   22  O7  UNL     1     -10.402   2.584  -1.405  1.00  0.00           O  
HETATM   23  C16 UNL     1      -8.653   1.817  -0.007  1.00  0.00           C  
HETATM   24  O8  UNL     1      -9.094   2.711   0.982  1.00  0.00           O  
HETATM   25  C17 UNL     1      -7.562   1.020   0.254  1.00  0.00           C  
HETATM   26  C18 UNL     1      -6.305  -1.943   0.333  1.00  0.00           C  
HETATM   27  C19 UNL     1      -5.138  -2.857   0.247  1.00  0.00           C  
HETATM   28  O9  UNL     1      -5.236  -4.094   0.113  1.00  0.00           O  
HETATM   29  C20 UNL     1       1.876  -0.269   1.919  1.00  0.00           C  
HETATM   30  O10 UNL     1       2.901  -1.154   2.238  1.00  0.00           O  
HETATM   31  C21 UNL     1       2.507   1.061   1.605  1.00  0.00           C  
HETATM   32  O11 UNL     1       2.226   1.927   2.661  1.00  0.00           O  
HETATM   33  C22 UNL     1       1.884   1.675   0.343  1.00  0.00           C  
HETATM   34  O12 UNL     1       2.528   2.881   0.129  1.00  0.00           O  
HETATM   35  C23 UNL     1       6.857   0.551  -1.030  1.00  0.00           C  
HETATM   36  C24 UNL     1       8.020   0.703  -1.740  1.00  0.00           C  
HETATM   37  C25 UNL     1       9.270   0.470  -1.159  1.00  0.00           C  
HETATM   38  O13 UNL     1      10.451   0.621  -1.871  1.00  0.00           O  
HETATM   39  C26 UNL     1       9.369   0.077   0.158  1.00  0.00           C  
HETATM   40  O14 UNL     1      10.608  -0.162   0.761  1.00  0.00           O  
HETATM   41  C27 UNL     1       8.213  -0.077   0.876  1.00  0.00           C  
HETATM   42  O15 UNL     1       8.260  -0.467   2.192  1.00  0.00           O  
HETATM   43  C28 UNL     1       6.967   0.159   0.284  1.00  0.00           C  
HETATM   44  H1  UNL     1       3.121   1.969  -2.108  1.00  0.00           H  
HETATM   45  H2  UNL     1       3.084   0.262  -2.586  1.00  0.00           H  
HETATM   46  H3  UNL     1       1.021   0.813  -1.383  1.00  0.00           H  
HETATM   47  H4  UNL     1       1.079  -1.942   0.801  1.00  0.00           H  
HETATM   48  H5  UNL     1      -0.565  -2.970   0.724  1.00  0.00           H  
HETATM   49  H6  UNL     1      -1.960  -4.942   0.756  1.00  0.00           H  
HETATM   50  H7  UNL     1      -2.422   0.842   0.197  1.00  0.00           H  
HETATM   51  H8  UNL     1      -5.672  -1.124  -1.536  1.00  0.00           H  
HETATM   52  H9  UNL     1      -7.502  -0.582  -2.714  1.00  0.00           H  
HETATM   53  H10 UNL     1      -9.452   0.859  -3.151  1.00  0.00           H  
HETATM   54  H11 UNL     1     -10.933   2.579  -2.282  1.00  0.00           H  
HETATM   55  H12 UNL     1      -8.650   2.794   1.868  1.00  0.00           H  
HETATM   56  H13 UNL     1      -7.022   1.046   1.188  1.00  0.00           H  
HETATM   57  H14 UNL     1      -6.312  -1.561   1.393  1.00  0.00           H  
HETATM   58  H15 UNL     1      -7.244  -2.441   0.058  1.00  0.00           H  
HETATM   59  H16 UNL     1       1.127  -0.163   2.724  1.00  0.00           H  
HETATM   60  H17 UNL     1       2.567  -2.045   2.503  1.00  0.00           H  
HETATM   61  H18 UNL     1       3.611   0.962   1.454  1.00  0.00           H  
HETATM   62  H19 UNL     1       2.096   1.459   3.519  1.00  0.00           H  
HETATM   63  H20 UNL     1       0.829   1.924   0.646  1.00  0.00           H  
HETATM   64  H21 UNL     1       3.107   3.144   0.875  1.00  0.00           H  
HETATM   65  H22 UNL     1       8.010   1.009  -2.777  1.00  0.00           H  
HETATM   66  H23 UNL     1      10.448   0.911  -2.853  1.00  0.00           H  
HETATM   67  H24 UNL     1      11.459  -0.046   0.225  1.00  0.00           H  
HETATM   68  H25 UNL     1       9.154  -0.639   2.626  1.00  0.00           H  
HETATM   69  H26 UNL     1       6.046   0.039   0.844  1.00  0.00           H  
CONECT    1    2    2
CONECT    2    3   35
CONECT    3    4
CONECT    4    5   44   45
CONECT    5    6   33   46
CONECT    6    7
CONECT    7    8   29   47
CONECT    8    9
CONECT    9   10   10   15
CONECT   10   11   48
CONECT   11   12   13   13
CONECT   12   49
CONECT   13   14   27
CONECT   14   15   15   16
CONECT   15   50
CONECT   16   17
CONECT   17   18   26   51
CONECT   18   19   19   25
CONECT   19   20   52
CONECT   20   21   21   53
CONECT   21   22   23
CONECT   22   54
CONECT   23   24   25   25
CONECT   24   55
CONECT   25   56
CONECT   26   27   57   58
CONECT   27   28   28
CONECT   29   30   31   59
CONECT   30   60
CONECT   31   32   33   61
CONECT   32   62
CONECT   33   34   63
CONECT   34   64
CONECT   35   36   36   43
CONECT   36   37   65
CONECT   37   38   39   39
CONECT   38   66
CONECT   39   40   41
CONECT   40   67
CONECT   41   42   43   43
CONECT   42   68
CONECT   43   69
END

HMDB0039921
     RDKit          3D
Eriodictyol 7-(6-galloylglucoside)
 69 73  0  0  0  0  0  0  0  0999 V2000
    5.5839    1.1612   -2.8868 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5871    0.8065   -1.6832 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3650    0.6844   -1.0630 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1316    0.9350   -1.7058 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9550    0.7242   -0.7912 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0045   -0.6193   -0.3753 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1507   -0.8457    0.7116 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1077   -0.2968    0.5345 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2941   -0.9759    0.4734 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4342   -2.3373    0.5795 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6752   -2.9827    0.5098 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7837   -4.3616    0.6207 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7965   -2.2339    0.3289 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7108   -0.8607    0.2162 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4827   -0.2431    0.2871 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8848   -0.1020    0.0292 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9782   -0.7539   -0.5474 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1416    0.1481   -0.7262 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8251    0.1081   -1.9221 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9188    0.8941   -2.2089 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3152    1.7593   -1.2021 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4022    2.5835   -1.4045 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6529    1.8168   -0.0074 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0940    2.7110    0.9816 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5616    1.0196    0.2539 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3050   -1.9426    0.3328 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1379   -2.8568    0.2471 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2361   -4.0940    0.1127 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8763   -0.2694    1.9188 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9009   -1.1543    2.2376 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5066    1.0614    1.6046 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2261    1.9268    2.6607 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8844    1.6754    0.3433 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5277    2.8805    0.1287 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8574    0.5511   -1.0296 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0205    0.7029   -1.7399 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2702    0.4701   -1.1592 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4509    0.6214   -1.8709 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.3691    0.0771    0.1582 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6078   -0.1616    0.7611 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.2125   -0.0772    0.8761 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2602   -0.4672    2.1922 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9671    0.1589    0.2837 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1209    1.9693   -2.1080 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0836    0.2625   -2.5859 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0208    0.8135   -1.3833 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0785   -1.9419    0.8005 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5647   -2.9696    0.7242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9601   -4.9415    0.7561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4224    0.8416    0.1973 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6716   -1.1241   -1.5359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5018   -0.5823   -2.7141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4525    0.8585   -3.1510 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.9330    2.5790   -2.2824 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6497    2.7939    1.8679 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0222    1.0461    1.1879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3122   -1.5607    1.3935 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2439   -2.4408    0.0577 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1268   -0.1629    2.7241 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5666   -2.0451    2.5035 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6108    0.9617    1.4545 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0962    1.4586    3.5190 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8289    1.9237    0.6460 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1066    3.1445    0.8745 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0099    1.0089   -2.7772 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.4481    0.9109   -2.8534 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.4586   -0.0458    0.2251 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1541   -0.6391    2.6260 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0464    0.0394    0.8438 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  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 11 13  2  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 23 25  2  0
 17 26  1  0
 26 27  1  0
 27 28  2  0
  7 29  1  0
 29 30  1  0
 29 31  1  0
 31 32  1  0
 31 33  1  0
 33 34  1  0
  2 35  1  0
 35 36  2  0
 36 37  1  0
 37 38  1  0
 37 39  2  0
 39 40  1  0
 39 41  1  0
 41 42  1  0
 41 43  2  0
 33  5  1  0
 43 35  1  0
 15  9  1  0
 25 18  1  0
 27 13  1  0
  4 44  1  0
  4 45  1  0
  5 46  1  0
  7 47  1  0
 10 48  1  0
 12 49  1  0
 15 50  1  0
 17 51  1  0
 19 52  1  0
 20 53  1  0
 22 54  1  0
 24 55  1  0
 25 56  1  0
 26 57  1  0
 26 58  1  0
 29 59  1  0
 30 60  1  0
 31 61  1  0
 32 62  1  0
 33 63  1  0
 34 64  1  0
 36 65  1  0
 38 66  1  0
 40 67  1  0
 42 68  1  0
 43 69  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
(6-{[2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-3,4-dihydro-2H-1-benzopyran-7-yl]oxy}-3,4,5-trihydroxyoxan-2-yl)methyl 3,4,5-trihydroxybenzoic acid	HMDB

Chemical Formula

C₂₈H₂₆O₁₅

Average Molecular Weight

602.497

Monoisotopic Molecular Weight

602.127170162

IUPAC Name

(6-{[2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-3,4-dihydro-2H-1-benzopyran-7-yl]oxy}-3,4,5-trihydroxyoxan-2-yl)methyl 3,4,5-trihydroxybenzoate

Traditional Name

(6-{[2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-2,3-dihydro-1-benzopyran-7-yl]oxy}-3,4,5-trihydroxyoxan-2-yl)methyl 3,4,5-trihydroxybenzoate

CAS Registry Number

Not Available

SMILES

OC1C(O)C(COC(=O)C2=CC(O)=C(O)C(O)=C2)OC(OC2=CC(O)=C3C(=O)CC(OC3=C2)C2=CC(O)=C(O)C=C2)C1O

InChI Identifier

InChI=1S/C28H26O15/c29-13-2-1-10(3-14(13)30)19-8-16(32)22-15(31)6-12(7-20(22)42-19)41-28-26(38)25(37)24(36)21(43-28)9-40-27(39)11-4-17(33)23(35)18(34)5-11/h1-7,19,21,24-26,28-31,33-38H,8-9H2

InChI Key

SHPCBRSOJXQRDY-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as flavonoid-7-o-glycosides. These are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C7-position.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Flavonoid glycosides

Direct Parent

Flavonoid-7-O-glycosides

Alternative Parents

Substituents

Flavonoid-7-o-glycoside
3'-hydroxyflavonoid
4'-hydroxyflavonoid
5-hydroxyflavonoid
Hydroxyflavonoid
Flavanone
Flavan
Phenolic glycoside
Galloyl ester
Gallic acid or derivatives
P-hydroxybenzoic acid alkyl ester
M-hydroxybenzoic acid ester
P-hydroxybenzoic acid ester
O-glycosyl compound
Glycosyl compound
Chromone
Benzoate ester
Chromane
1-benzopyran
Benzopyran
Benzoic acid or derivatives
Benzenetriol
Pyrogallol derivative
Benzoyl
Catechol
Aryl alkyl ketone
Aryl ketone
Phenol
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
1-hydroxy-4-unsubstituted benzenoid
Oxane
Benzenoid
Monosaccharide
Monocyclic benzene moiety
Vinylogous acid
Ketone
Secondary alcohol
Carboxylic acid ester
Polyol
Acetal
Monocarboxylic acid or derivatives
Ether
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Alcohol
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Extracellular (HMDB: HMDB0039921)
Cytoplasm (HMDB: HMDB0039921)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0039921)

Source

Exogenous

Food

Food (HMDB: HMDB0039921)

Fruit

Fruits (FooDB: FOOD00871)

Endogenous

Plant

Plant (HMDB: HMDB0039921)

Not Available

Nutrient (HMDB: HMDB0039921)

Physical Properties

State

Not Available

Experimental Molecular Properties

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

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.49 g/L	ALOGPS
logP	1.5	ALOGPS
logP	1.85	ChemAxon
logS	-3.1	ALOGPS
pKa (Strongest Acidic)	8.07	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	14	ChemAxon
Hydrogen Donor Count	9	ChemAxon
Polar Surface Area	253.13 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	141.18 m³·mol⁻¹	ChemAxon
Polarizability	56.66 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
DarkChem	[M+H]+	232.616	31661259
DarkChem	[M-H]-	229.749	31661259
DeepCCS	[M+H]+	228.989	30932474
DeepCCS	[M-H]-	227.103	30932474
DeepCCS	[M-2H]-	260.341	30932474
DeepCCS	[M+Na]+	234.658	30932474
AllCCS	[M+H]+	231.1	32859911
AllCCS	[M+H-H2O]+	229.9	32859911
AllCCS	[M+NH4]+	232.2	32859911
AllCCS	[M+Na]+	232.5	32859911
AllCCS	[M-H]-	226.2	32859911
AllCCS	[M+Na-2H]-	228.1	32859911
AllCCS	[M+HCOO]-	230.4	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Eriodictyol 7-(6-galloylglucoside)	OC1C(O)C(COC(=O)C2=CC(O)=C(O)C(O)=C2)OC(OC2=CC(O)=C3C(=O)CC(OC3=C2)C2=CC(O)=C(O)C=C2)C1O	6463.1	Standard polar	33892256
Eriodictyol 7-(6-galloylglucoside)	OC1C(O)C(COC(=O)C2=CC(O)=C(O)C(O)=C2)OC(OC2=CC(O)=C3C(=O)CC(OC3=C2)C2=CC(O)=C(O)C=C2)C1O	5205.6	Standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside)	OC1C(O)C(COC(=O)C2=CC(O)=C(O)C(O)=C2)OC(OC2=CC(O)=C3C(=O)CC(OC3=C2)C2=CC(O)=C(O)C=C2)C1O	5721.9	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Eriodictyol 7-(6-galloylglucoside),1TMS,isomer #1	C[Si](C)(C)OC1C(O)C(COC(=O)C2=CC(O)=C(O)C(O)=C2)OC(OC2=CC(O)=C3C(=O)CC(C4=CC=C(O)C(O)=C4)OC3=C2)C1O	5714.5	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),1TMS,isomer #2	C[Si](C)(C)OC1C(COC(=O)C2=CC(O)=C(O)C(O)=C2)OC(OC2=CC(O)=C3C(=O)CC(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C1O	5688.2	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),1TMS,isomer #3	C[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC(O)=C4C(=O)CC(C5=CC=C(O)C(O)=C5)OC4=C3)C(O)C(O)C2O)=CC(O)=C1O	5709.3	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),1TMS,isomer #4	C[Si](C)(C)OC1=C(O)C=C(C(=O)OCC2OC(OC3=CC(O)=C4C(=O)CC(C5=CC=C(O)C(O)=C5)OC4=C3)C(O)C(O)C2O)C=C1O	5691.0	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),1TMS,isomer #5	C[Si](C)(C)OC1=CC(OC2OC(COC(=O)C3=CC(O)=C(O)C(O)=C3)C(O)C(O)C2O)=CC2=C1C(=O)CC(C1=CC=C(O)C(O)=C1)O2	5676.1	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),1TMS,isomer #6	C[Si](C)(C)OC1=CC(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O)C(O)C4O)C=C3O2)=CC=C1O	5738.9	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),1TMS,isomer #7	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O)C(O)C4O)C=C3O2)C=C1O	5763.6	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),1TMS,isomer #8	C[Si](C)(C)OC1C(OC2=CC(O)=C3C(=O)CC(C4=CC=C(O)C(O)=C4)OC3=C2)OC(COC(=O)C2=CC(O)=C(O)C(O)=C2)C(O)C1O	5706.5	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TMS,isomer #1	C[Si](C)(C)OC1C(COC(=O)C2=CC(O)=C(O)C(O)=C2)OC(OC2=CC(O)=C3C(=O)CC(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C1O[Si](C)(C)C	5674.8	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TMS,isomer #10	C[Si](C)(C)OC1=CC(OC2OC(COC(=O)C3=CC(O)=C(O)C(O)=C3)C(O[Si](C)(C)C)C(O)C2O)=CC2=C1C(=O)CC(C1=CC=C(O)C(O)=C1)O2	5635.2	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TMS,isomer #11	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)C=C1O	5650.1	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TMS,isomer #12	C[Si](C)(C)OC1=CC(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)=CC=C1O	5623.9	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TMS,isomer #13	C[Si](C)(C)OC1C(COC(=O)C2=CC(O)=C(O)C(O)=C2)OC(OC2=CC(O)=C3C(=O)CC(C4=CC=C(O)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C1O	5694.1	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TMS,isomer #14	C[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC4=C(C(=O)CC(C5=CC=C(O)C(O)=C5)O4)C(O[Si](C)(C)C)=C3)C(O)C(O)C2O)=CC(O)=C1O	5641.6	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TMS,isomer #15	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O[Si](C)(C)C)=C5)C(O)C(O)C4O)C=C3O2)C=C1O	5621.2	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TMS,isomer #16	C[Si](C)(C)OC1=CC(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O[Si](C)(C)C)=C5)C(O)C(O)C4O)C=C3O2)=CC=C1O	5590.0	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TMS,isomer #17	C[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC(O)=C4C(=O)CC(C5=CC=C(O)C(O)=C5)OC4=C3)C(O[Si](C)(C)C)C(O)C2O)=CC(O)=C1O	5632.9	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TMS,isomer #18	C[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC(O)=C4C(=O)CC(C5=CC=C(O)C(O)=C5)OC4=C3)C(O)C(O)C2O)=CC(O[Si](C)(C)C)=C1O	5624.6	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TMS,isomer #19	C[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC(O)=C4C(=O)CC(C5=CC=C(O)C(O)=C5)OC4=C3)C(O)C(O)C2O)=CC(O)=C1O[Si](C)(C)C	5546.4	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TMS,isomer #2	C[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC(O)=C4C(=O)CC(C5=CC=C(O)C(O)=C5)OC4=C3)C(O)C(O[Si](C)(C)C)C2O)=CC(O)=C1O	5618.2	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TMS,isomer #20	C[Si](C)(C)OC1=CC(OC2OC(COC(=O)C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C(O)C(O)C2O)=CC2=C1C(=O)CC(C1=CC=C(O)C(O)=C1)O2	5613.5	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TMS,isomer #21	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O[Si](C)(C)C)C(O)=C5)C(O)C(O)C4O)C=C3O2)C=C1O	5590.4	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TMS,isomer #22	C[Si](C)(C)OC1=CC(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O[Si](C)(C)C)C(O)=C5)C(O)C(O)C4O)C=C3O2)=CC=C1O	5554.5	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TMS,isomer #23	C[Si](C)(C)OC1=C(O)C=C(C(=O)OCC2OC(OC3=CC(O)=C4C(=O)CC(C5=CC=C(O)C(O)=C5)OC4=C3)C(O[Si](C)(C)C)C(O)C2O)C=C1O	5600.2	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TMS,isomer #24	C[Si](C)(C)OC1=CC(OC2OC(COC(=O)C3=CC(O)=C(O)C(O)=C3)C(O)C(O)C2O[Si](C)(C)C)=CC2=C1C(=O)CC(C1=CC=C(O)C(O)=C1)O2	5655.1	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TMS,isomer #25	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O)C(O)C4O)C=C3O[Si](C)(C)C)O2)C=C1O	5681.0	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TMS,isomer #26	C[Si](C)(C)OC1=CC(C2CC(=O)C3=C(C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O)C(O)C4O)C=C3O[Si](C)(C)C)O2)=CC=C1O	5655.7	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TMS,isomer #27	C[Si](C)(C)OC1=CC(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)=CC=C1O	5647.2	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TMS,isomer #28	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O)C(O)C4O)C=C3O2)C=C1O[Si](C)(C)C	5656.1	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TMS,isomer #29	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1O	5669.2	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TMS,isomer #3	C[Si](C)(C)OC1=C(O)C=C(C(=O)OCC2OC(OC3=CC(O)=C4C(=O)CC(C5=CC=C(O)C(O)=C5)OC4=C3)C(O)C(O[Si](C)(C)C)C2O)C=C1O	5588.5	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TMS,isomer #4	C[Si](C)(C)OC1=CC(OC2OC(COC(=O)C3=CC(O)=C(O)C(O)=C3)C(O)C(O[Si](C)(C)C)C2O)=CC2=C1C(=O)CC(C1=CC=C(O)C(O)=C1)O2	5654.7	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TMS,isomer #5	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1O	5659.8	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TMS,isomer #6	C[Si](C)(C)OC1=CC(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)=CC=C1O	5628.9	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TMS,isomer #7	C[Si](C)(C)OC1C(OC2=CC(O)=C3C(=O)CC(C4=CC=C(O)C(O)=C4)OC3=C2)OC(COC(=O)C2=CC(O)=C(O)C(O)=C2)C(O)C1O[Si](C)(C)C	5654.9	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TMS,isomer #8	C[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC(O)=C4C(=O)CC(C5=CC=C(O)C(O)=C5)OC4=C3)C(O)C(O)C2O[Si](C)(C)C)=CC(O)=C1O	5609.9	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TMS,isomer #9	C[Si](C)(C)OC1=C(O)C=C(C(=O)OCC2OC(OC3=CC(O)=C4C(=O)CC(C5=CC=C(O)C(O)=C5)OC4=C3)C(O)C(O)C2O[Si](C)(C)C)C=C1O	5579.2	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #1	C[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC(O)=C4C(=O)CC(C5=CC=C(O)C(O)=C5)OC4=C3)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC(O)=C1O	5494.9	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #10	C[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC(O)=C4C(=O)CC(C5=CC=C(O)C(O)=C5)OC4=C3)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)=CC(O)=C1O	5489.1	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #11	C[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC(O)=C4C(=O)CC(C5=CC=C(O)C(O)=C5)OC4=C3)C(O)C(O[Si](C)(C)C)C2O)=CC(O[Si](C)(C)C)=C1O	5425.7	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #12	C[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC(O)=C4C(=O)CC(C5=CC=C(O)C(O)=C5)OC4=C3)C(O)C(O[Si](C)(C)C)C2O)=CC(O)=C1O[Si](C)(C)C	5377.4	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #13	C[Si](C)(C)OC1=CC(OC2OC(COC(=O)C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C(O)C(O[Si](C)(C)C)C2O)=CC2=C1C(=O)CC(C1=CC=C(O)C(O)=C1)O2	5436.9	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #14	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O[Si](C)(C)C)C(O)=C5)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1O	5415.3	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #15	C[Si](C)(C)OC1=CC(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O[Si](C)(C)C)C(O)=C5)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)=CC=C1O	5384.6	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #16	C[Si](C)(C)OC1=C(O)C=C(C(=O)OCC2OC(OC3=CC(O)=C4C(=O)CC(C5=CC=C(O)C(O)=C5)OC4=C3)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=C1O	5463.7	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #17	C[Si](C)(C)OC1=CC(OC2OC(COC(=O)C3=CC(O)=C(O)C(O)=C3)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC2=C1C(=O)CC(C1=CC=C(O)C(O)=C1)O2	5578.3	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #18	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O)C(O[Si](C)(C)C)C4O)C=C3O[Si](C)(C)C)O2)C=C1O	5508.8	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #19	C[Si](C)(C)OC1=CC(C2CC(=O)C3=C(C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O)C(O[Si](C)(C)C)C4O)C=C3O[Si](C)(C)C)O2)=CC=C1O	5480.6	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #2	C[Si](C)(C)OC1=C(O)C=C(C(=O)OCC2OC(OC3=CC(O)=C4C(=O)CC(C5=CC=C(O)C(O)=C5)OC4=C3)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=C1O	5467.8	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #20	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)C=C1O	5525.5	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #21	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1O[Si](C)(C)C	5494.7	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #22	C[Si](C)(C)OC1=CC(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)=CC=C1O	5503.7	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #23	C[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC4=C(C(=O)CC(C5=CC=C(O)C(O)=C5)O4)C(O[Si](C)(C)C)=C3)C(O)C(O)C2O[Si](C)(C)C)=CC(O)=C1O	5498.8	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #24	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O[Si](C)(C)C)=C5)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)C=C1O	5407.0	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #25	C[Si](C)(C)OC1=CC(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O[Si](C)(C)C)=C5)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)=CC=C1O	5386.5	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #26	C[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC(O)=C4C(=O)CC(C5=CC=C(O)C(O)=C5)OC4=C3)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)=CC(O)=C1O	5533.3	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #27	C[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC(O)=C4C(=O)CC(C5=CC=C(O)C(O)=C5)OC4=C3)C(O)C(O)C2O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O	5452.0	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #28	C[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC(O)=C4C(=O)CC(C5=CC=C(O)C(O)=C5)OC4=C3)C(O)C(O)C2O[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C	5401.1	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #29	C[Si](C)(C)OC1=CC(OC2OC(COC(=O)C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C(O[Si](C)(C)C)C(O)C2O)=CC2=C1C(=O)CC(C1=CC=C(O)C(O)=C1)O2	5454.0	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #3	C[Si](C)(C)OC1=CC(OC2OC(COC(=O)C3=CC(O)=C(O)C(O)=C3)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)=CC2=C1C(=O)CC(C1=CC=C(O)C(O)=C1)O2	5588.8	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #30	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O[Si](C)(C)C)C(O)=C5)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)C=C1O	5402.6	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #31	C[Si](C)(C)OC1=CC(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O[Si](C)(C)C)C(O)=C5)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)=CC=C1O	5382.1	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #32	C[Si](C)(C)OC1=C(O)C=C(C(=O)OCC2OC(OC3=CC(O)=C4C(=O)CC(C5=CC=C(O)C(O)=C5)OC4=C3)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=C1O	5505.0	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #33	C[Si](C)(C)OC1=CC(OC2OC(COC(=O)C3=CC(O)=C(O)C(O)=C3)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)=CC2=C1C(=O)CC(C1=CC=C(O)C(O)=C1)O2	5606.6	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #34	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O[Si](C)(C)C)C(O)C4O)C=C3O[Si](C)(C)C)O2)C=C1O	5524.4	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #35	C[Si](C)(C)OC1=CC(C2CC(=O)C3=C(C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O[Si](C)(C)C)C(O)C4O)C=C3O[Si](C)(C)C)O2)=CC=C1O	5504.8	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #36	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1O	5561.8	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #37	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)C=C1O[Si](C)(C)C	5505.7	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #38	C[Si](C)(C)OC1=CC(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C=C3O2)=CC=C1O	5540.5	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #39	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O[Si](C)(C)C)=C5)C(O)C(O)C4O)C=C3O[Si](C)(C)C)O2)C=C1O	5437.7	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #4	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1O	5534.5	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #40	C[Si](C)(C)OC1=CC(C2CC(=O)C3=C(C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O[Si](C)(C)C)=C5)C(O)C(O)C4O)C=C3O[Si](C)(C)C)O2)=CC=C1O	5410.7	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #41	C[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC4=C(C(=O)CC(C5=CC=C(O)C(O)=C5)O4)C(O[Si](C)(C)C)=C3)C(O[Si](C)(C)C)C(O)C2O)=CC(O)=C1O	5522.3	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #42	C[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC4=C(C(=O)CC(C5=CC=C(O)C(O)=C5)O4)C(O[Si](C)(C)C)=C3)C(O)C(O)C2O)=CC(O[Si](C)(C)C)=C1O	5484.6	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #43	C[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC4=C(C(=O)CC(C5=CC=C(O)C(O)=C5)O4)C(O[Si](C)(C)C)=C3)C(O)C(O)C2O)=CC(O)=C1O[Si](C)(C)C	5425.3	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #44	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C5)C(O)C(O)C4O)C=C3O2)C=C1O	5417.1	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #45	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)C(O)C(O)C4O)C=C3O2)C=C1O	5354.5	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #46	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O[Si](C)(C)C)=C5)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1O	5433.2	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #47	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O[Si](C)(C)C)=C5)C(O)C(O)C4O)C=C3O2)C=C1O[Si](C)(C)C	5428.7	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #48	C[Si](C)(C)OC1=CC(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C5)C(O)C(O)C4O)C=C3O2)=CC=C1O	5398.7	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #49	C[Si](C)(C)OC1=CC(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)C(O)C(O)C4O)C=C3O2)=CC=C1O	5329.8	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #5	C[Si](C)(C)OC1=CC(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C=C3O2)=CC=C1O	5507.1	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #50	C[Si](C)(C)OC1=CC(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O[Si](C)(C)C)=C5)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)=CC=C1O	5408.2	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #51	C[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC(O)=C4C(=O)CC(C5=CC=C(O)C(O)=C5)OC4=C3)C(O[Si](C)(C)C)C(O)C2O)=CC(O[Si](C)(C)C)=C1O	5477.5	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #52	C[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC(O)=C4C(=O)CC(C5=CC=C(O)C(O)=C5)OC4=C3)C(O[Si](C)(C)C)C(O)C2O)=CC(O)=C1O[Si](C)(C)C	5426.6	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #53	C[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC(O)=C4C(=O)CC(C5=CC=C(O)C(O)=C5)OC4=C3)C(O)C(O)C2O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C	5403.5	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #54	C[Si](C)(C)OC1=CC(OC2OC(COC(=O)C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C(O)C(O)C2O[Si](C)(C)C)=CC2=C1C(=O)CC(C1=CC=C(O)C(O)=C1)O2	5484.3	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #55	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(C=C(OC4OC(COC(=O)C5=CC(O)=C(O[Si](C)(C)C)C(O)=C5)C(O)C(O)C4O)C=C3O[Si](C)(C)C)O2)C=C1O	5401.6	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #56	C[Si](C)(C)OC1=CC(C2CC(=O)C3=C(C=C(OC4OC(COC(=O)C5=CC(O)=C(O[Si](C)(C)C)C(O)=C5)C(O)C(O)C4O)C=C3O[Si](C)(C)C)O2)=CC=C1O	5376.8	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #57	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O[Si](C)(C)C)C(O)=C5)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1O	5409.4	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #58	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O[Si](C)(C)C)C(O)=C5)C(O)C(O)C4O)C=C3O2)C=C1O[Si](C)(C)C	5392.9	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #59	C[Si](C)(C)OC1=CC(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O[Si](C)(C)C)C(O)=C5)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)=CC=C1O	5381.6	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #6	C[Si](C)(C)OC1C(COC(=O)C2=CC(O)=C(O)C(O)=C2)OC(OC2=CC(O)=C3C(=O)CC(C4=CC=C(O)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5627.9	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #60	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O)C(O)C4O[Si](C)(C)C)C=C3O[Si](C)(C)C)O2)C=C1O	5550.0	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #61	C[Si](C)(C)OC1=CC(C2CC(=O)C3=C(C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O)C(O)C4O[Si](C)(C)C)C=C3O[Si](C)(C)C)O2)=CC=C1O	5531.0	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #62	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O)C(O)C4O)C=C3O[Si](C)(C)C)O2)C=C1O[Si](C)(C)C	5535.7	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #63	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1O[Si](C)(C)C	5537.2	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #7	C[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC4=C(C(=O)CC(C5=CC=C(O)C(O)=C5)O4)C(O[Si](C)(C)C)=C3)C(O)C(O[Si](C)(C)C)C2O)=CC(O)=C1O	5484.0	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #8	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O[Si](C)(C)C)=C5)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1O	5376.4	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),3TMS,isomer #9	C[Si](C)(C)OC1=CC(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O[Si](C)(C)C)=C5)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)=CC=C1O	5350.7	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #1	C[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC4=C(C(=O)CC(C5=CC=C(O)C(O)=C5)O4)C(O[Si](C)(C)C)=C3)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC(O)=C1O	5353.8	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #10	C[Si](C)(C)OC1=C(O)C=C(C(=O)OCC2OC(OC3=CC(O)=C4C(=O)CC(C5=CC=C(O)C(O)=C5)OC4=C3)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=C1O	5362.2	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #11	C[Si](C)(C)OC1=CC(OC2OC(COC(=O)C3=CC(O)=C(O)C(O)=C3)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC2=C1C(=O)CC(C1=CC=C(O)C(O)=C1)O2	5500.3	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #12	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C=C3O[Si](C)(C)C)O2)C=C1O	5388.9	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #13	C[Si](C)(C)OC1=CC(C2CC(=O)C3=C(C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C=C3O[Si](C)(C)C)O2)=CC=C1O	5353.7	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #14	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)C=C1O	5435.2	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #15	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1O[Si](C)(C)C	5395.4	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #16	C[Si](C)(C)OC1=CC(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)=CC=C1O	5406.2	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #17	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O[Si](C)(C)C)=C5)C(O)C(O[Si](C)(C)C)C4O)C=C3O[Si](C)(C)C)O2)C=C1O	5206.1	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #18	C[Si](C)(C)OC1=CC(C2CC(=O)C3=C(C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O[Si](C)(C)C)=C5)C(O)C(O[Si](C)(C)C)C4O)C=C3O[Si](C)(C)C)O2)=CC=C1O	5177.0	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #19	C[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC4=C(C(=O)CC(C5=CC=C(O)C(O)=C5)O4)C(O[Si](C)(C)C)=C3)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)=CC(O)=C1O	5366.7	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #2	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O[Si](C)(C)C)=C5)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1O	5258.5	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #20	C[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC4=C(C(=O)CC(C5=CC=C(O)C(O)=C5)O4)C(O[Si](C)(C)C)=C3)C(O)C(O[Si](C)(C)C)C2O)=CC(O[Si](C)(C)C)=C1O	5264.6	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #21	C[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC4=C(C(=O)CC(C5=CC=C(O)C(O)=C5)O4)C(O[Si](C)(C)C)=C3)C(O)C(O[Si](C)(C)C)C2O)=CC(O)=C1O[Si](C)(C)C	5211.6	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #22	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C5)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1O	5244.3	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #23	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1O	5214.9	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #24	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O[Si](C)(C)C)=C5)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)C=C1O	5271.6	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #25	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O[Si](C)(C)C)=C5)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1O[Si](C)(C)C	5226.4	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #26	C[Si](C)(C)OC1=CC(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C5)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)=CC=C1O	5218.1	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #27	C[Si](C)(C)OC1=CC(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)=CC=C1O	5186.9	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #28	C[Si](C)(C)OC1=CC(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O[Si](C)(C)C)=C5)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)=CC=C1O	5249.5	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #29	C[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC(O)=C4C(=O)CC(C5=CC=C(O)C(O)=C5)OC4=C3)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)=CC(O[Si](C)(C)C)=C1O	5312.5	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #3	C[Si](C)(C)OC1=CC(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O[Si](C)(C)C)=C5)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C=C3O2)=CC=C1O	5238.9	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #30	C[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC(O)=C4C(=O)CC(C5=CC=C(O)C(O)=C5)OC4=C3)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)=CC(O)=C1O[Si](C)(C)C	5268.2	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #31	C[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC(O)=C4C(=O)CC(C5=CC=C(O)C(O)=C5)OC4=C3)C(O)C(O[Si](C)(C)C)C2O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C	5216.3	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #32	C[Si](C)(C)OC1=CC(OC2OC(COC(=O)C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC2=C1C(=O)CC(C1=CC=C(O)C(O)=C1)O2	5313.1	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #33	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(C=C(OC4OC(COC(=O)C5=CC(O)=C(O[Si](C)(C)C)C(O)=C5)C(O)C(O[Si](C)(C)C)C4O)C=C3O[Si](C)(C)C)O2)C=C1O	5248.4	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #34	C[Si](C)(C)OC1=CC(C2CC(=O)C3=C(C=C(OC4OC(COC(=O)C5=CC(O)=C(O[Si](C)(C)C)C(O)=C5)C(O)C(O[Si](C)(C)C)C4O)C=C3O[Si](C)(C)C)O2)=CC=C1O	5215.9	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #35	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O[Si](C)(C)C)C(O)=C5)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)C=C1O	5285.2	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #36	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O[Si](C)(C)C)C(O)=C5)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1O[Si](C)(C)C	5268.7	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #37	C[Si](C)(C)OC1=CC(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O[Si](C)(C)C)C(O)=C5)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)=CC=C1O	5260.6	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #38	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O[Si](C)(C)C)O2)C=C1O	5400.9	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #39	C[Si](C)(C)OC1=CC(C2CC(=O)C3=C(C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O[Si](C)(C)C)O2)=CC=C1O	5372.0	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #4	C[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC(O)=C4C(=O)CC(C5=CC=C(O)C(O)=C5)OC4=C3)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC(O)=C1O	5401.8	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #40	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O)C(O[Si](C)(C)C)C4O)C=C3O[Si](C)(C)C)O2)C=C1O[Si](C)(C)C	5355.8	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #41	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)C=C1O[Si](C)(C)C	5410.1	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #42	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O[Si](C)(C)C)=C5)C(O[Si](C)(C)C)C(O)C4O)C=C3O[Si](C)(C)C)O2)C=C1O	5249.0	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #43	C[Si](C)(C)OC1=CC(C2CC(=O)C3=C(C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O[Si](C)(C)C)=C5)C(O[Si](C)(C)C)C(O)C4O)C=C3O[Si](C)(C)C)O2)=CC=C1O	5226.8	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #44	C[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC4=C(C(=O)CC(C5=CC=C(O)C(O)=C5)O4)C(O[Si](C)(C)C)=C3)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)=CC(O)=C1O	5391.2	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #45	C[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC4=C(C(=O)CC(C5=CC=C(O)C(O)=C5)O4)C(O[Si](C)(C)C)=C3)C(O)C(O)C2O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O	5318.0	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #46	C[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC4=C(C(=O)CC(C5=CC=C(O)C(O)=C5)O4)C(O[Si](C)(C)C)=C3)C(O)C(O)C2O[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C	5261.3	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #47	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C5)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)C=C1O	5259.2	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #48	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)C=C1O	5218.3	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #49	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O[Si](C)(C)C)=C5)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1O	5294.5	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #5	C[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC(O)=C4C(=O)CC(C5=CC=C(O)C(O)=C5)OC4=C3)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O	5297.6	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #50	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O[Si](C)(C)C)=C5)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)C=C1O[Si](C)(C)C	5264.7	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #51	C[Si](C)(C)OC1=CC(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C5)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)=CC=C1O	5245.7	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #52	C[Si](C)(C)OC1=CC(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)=CC=C1O	5198.0	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #53	C[Si](C)(C)OC1=CC(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O[Si](C)(C)C)=C5)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C=C3O2)=CC=C1O	5269.9	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #54	C[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC(O)=C4C(=O)CC(C5=CC=C(O)C(O)=C5)OC4=C3)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O	5341.3	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #55	C[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC(O)=C4C(=O)CC(C5=CC=C(O)C(O)=C5)OC4=C3)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C	5299.7	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #56	C[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC(O)=C4C(=O)CC(C5=CC=C(O)C(O)=C5)OC4=C3)C(O)C(O)C2O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C	5255.2	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #57	C[Si](C)(C)OC1=CC(OC2OC(COC(=O)C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)=CC2=C1C(=O)CC(C1=CC=C(O)C(O)=C1)O2	5340.4	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #58	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(C=C(OC4OC(COC(=O)C5=CC(O)=C(O[Si](C)(C)C)C(O)=C5)C(O[Si](C)(C)C)C(O)C4O)C=C3O[Si](C)(C)C)O2)C=C1O	5241.8	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #59	C[Si](C)(C)OC1=CC(C2CC(=O)C3=C(C=C(OC4OC(COC(=O)C5=CC(O)=C(O[Si](C)(C)C)C(O)=C5)C(O[Si](C)(C)C)C(O)C4O)C=C3O[Si](C)(C)C)O2)=CC=C1O	5217.6	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #6	C[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC(O)=C4C(=O)CC(C5=CC=C(O)C(O)=C5)OC4=C3)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C	5253.5	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #60	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O[Si](C)(C)C)C(O)=C5)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1O	5306.7	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #61	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O[Si](C)(C)C)C(O)=C5)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)C=C1O[Si](C)(C)C	5263.9	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #62	C[Si](C)(C)OC1=CC(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O[Si](C)(C)C)C(O)=C5)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C=C3O2)=CC=C1O	5283.2	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #63	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C=C3O[Si](C)(C)C)O2)C=C1O	5425.0	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #64	C[Si](C)(C)OC1=CC(C2CC(=O)C3=C(C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C=C3O[Si](C)(C)C)O2)=CC=C1O	5400.5	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #65	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O[Si](C)(C)C)C(O)C4O)C=C3O[Si](C)(C)C)O2)C=C1O[Si](C)(C)C	5383.8	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #66	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1O[Si](C)(C)C	5432.5	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #67	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(C=C(OC4OC(COC(=O)C5=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C5)C(O)C(O)C4O)C=C3O[Si](C)(C)C)O2)C=C1O	5265.2	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #68	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(C=C(OC4OC(COC(=O)C5=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)C(O)C(O)C4O)C=C3O[Si](C)(C)C)O2)C=C1O	5203.2	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #69	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O[Si](C)(C)C)=C5)C(O)C(O)C4O[Si](C)(C)C)C=C3O[Si](C)(C)C)O2)C=C1O	5271.4	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #7	C[Si](C)(C)OC1=CC(OC2OC(COC(=O)C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)=CC2=C1C(=O)CC(C1=CC=C(O)C(O)=C1)O2	5295.9	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #70	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O[Si](C)(C)C)=C5)C(O)C(O)C4O)C=C3O[Si](C)(C)C)O2)C=C1O[Si](C)(C)C	5270.2	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #71	C[Si](C)(C)OC1=CC(C2CC(=O)C3=C(C=C(OC4OC(COC(=O)C5=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C5)C(O)C(O)C4O)C=C3O[Si](C)(C)C)O2)=CC=C1O	5244.0	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #72	C[Si](C)(C)OC1=CC(C2CC(=O)C3=C(C=C(OC4OC(COC(=O)C5=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)C(O)C(O)C4O)C=C3O[Si](C)(C)C)O2)=CC=C1O	5178.1	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #73	C[Si](C)(C)OC1=CC(C2CC(=O)C3=C(C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O[Si](C)(C)C)=C5)C(O)C(O)C4O[Si](C)(C)C)C=C3O[Si](C)(C)C)O2)=CC=C1O	5245.0	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #74	C[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC4=C(C(=O)CC(C5=CC=C(O)C(O)=C5)O4)C(O[Si](C)(C)C)=C3)C(O[Si](C)(C)C)C(O)C2O)=CC(O[Si](C)(C)C)=C1O	5352.8	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #75	C[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC4=C(C(=O)CC(C5=CC=C(O)C(O)=C5)O4)C(O[Si](C)(C)C)=C3)C(O[Si](C)(C)C)C(O)C2O)=CC(O)=C1O[Si](C)(C)C	5301.0	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #76	C[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC4=C(C(=O)CC(C5=CC=C(O)C(O)=C5)O4)C(O[Si](C)(C)C)=C3)C(O)C(O)C2O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C	5283.3	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #77	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)C(O)C(O)C4O)C=C3O2)C=C1O	5212.2	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #78	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C5)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1O	5272.0	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #79	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C5)C(O)C(O)C4O)C=C3O2)C=C1O[Si](C)(C)C	5273.6	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #8	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O[Si](C)(C)C)C(O)=C5)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1O	5285.6	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #80	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1O	5219.8	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #81	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)C(O)C(O)C4O)C=C3O2)C=C1O[Si](C)(C)C	5214.2	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #82	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O[Si](C)(C)C)=C5)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1O[Si](C)(C)C	5286.7	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #83	C[Si](C)(C)OC1=CC(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)C(O)C(O)C4O)C=C3O2)=CC=C1O	5188.1	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #84	C[Si](C)(C)OC1=CC(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C5)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)=CC=C1O	5253.3	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #85	C[Si](C)(C)OC1=CC(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)=CC=C1O	5195.3	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #86	C[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC(O)=C4C(=O)CC(C5=CC=C(O)C(O)=C5)OC4=C3)C(O[Si](C)(C)C)C(O)C2O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C	5292.2	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #87	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(C=C(OC4OC(COC(=O)C5=CC(O)=C(O[Si](C)(C)C)C(O)=C5)C(O)C(O)C4O[Si](C)(C)C)C=C3O[Si](C)(C)C)O2)C=C1O	5245.7	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #88	C[Si](C)(C)OC1=CC(C2CC(=O)C3=C(C=C(OC4OC(COC(=O)C5=CC(O)=C(O[Si](C)(C)C)C(O)=C5)C(O)C(O)C4O[Si](C)(C)C)C=C3O[Si](C)(C)C)O2)=CC=C1O	5221.3	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #89	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(C=C(OC4OC(COC(=O)C5=CC(O)=C(O[Si](C)(C)C)C(O)=C5)C(O)C(O)C4O)C=C3O[Si](C)(C)C)O2)C=C1O[Si](C)(C)C	5244.2	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #9	C[Si](C)(C)OC1=CC(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O[Si](C)(C)C)C(O)=C5)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C=C3O2)=CC=C1O	5263.3	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #90	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O[Si](C)(C)C)C(O)=C5)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1O[Si](C)(C)C	5267.7	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),4TMS,isomer #91	C[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O)C(O)C4O[Si](C)(C)C)C=C3O[Si](C)(C)C)O2)C=C1O[Si](C)(C)C	5419.8	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC1C(O)C(COC(=O)C2=CC(O)=C(O)C(O)=C2)OC(OC2=CC(O)=C3C(=O)CC(C4=CC=C(O)C(O)=C4)OC3=C2)C1O	5985.9	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1C(COC(=O)C2=CC(O)=C(O)C(O)=C2)OC(OC2=CC(O)=C3C(=O)CC(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C1O	5961.0	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC(O)=C4C(=O)CC(C5=CC=C(O)C(O)=C5)OC4=C3)C(O)C(O)C2O)=CC(O)=C1O	5945.9	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC1=C(O)C=C(C(=O)OCC2OC(OC3=CC(O)=C4C(=O)CC(C5=CC=C(O)C(O)=C5)OC4=C3)C(O)C(O)C2O)C=C1O	5966.3	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC1=CC(OC2OC(COC(=O)C3=CC(O)=C(O)C(O)=C3)C(O)C(O)C2O)=CC2=C1C(=O)CC(C1=CC=C(O)C(O)=C1)O2	5920.7	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),1TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC1=CC(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O)C(O)C4O)C=C3O2)=CC=C1O	5976.1	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),1TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O)C(O)C4O)C=C3O2)C=C1O	5995.4	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),1TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC1C(OC2=CC(O)=C3C(=O)CC(C4=CC=C(O)C(O)=C4)OC3=C2)OC(COC(=O)C2=CC(O)=C(O)C(O)=C2)C(O)C1O	5983.5	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC1C(COC(=O)C2=CC(O)=C(O)C(O)=C2)OC(OC2=CC(O)=C3C(=O)CC(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C1O[Si](C)(C)C(C)(C)C	6176.0	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC1=CC(OC2OC(COC(=O)C3=CC(O)=C(O)C(O)=C3)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)=CC2=C1C(=O)CC(C1=CC=C(O)C(O)=C1)O2	6117.9	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O[Si](C)(C)C(C)(C)C)C(O)C4O)C=C3O2)C=C1O	6104.0	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC1=CC(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O[Si](C)(C)C(C)(C)C)C(O)C4O)C=C3O2)=CC=C1O	6076.5	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC1C(COC(=O)C2=CC(O)=C(O)C(O)=C2)OC(OC2=CC(O)=C3C(=O)CC(C4=CC=C(O)C(O)=C4)OC3=C2)C(O[Si](C)(C)C(C)(C)C)C1O	6192.8	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC4=C(C(=O)CC(C5=CC=C(O)C(O)=C5)O4)C(O[Si](C)(C)C(C)(C)C)=C3)C(O)C(O)C2O)=CC(O)=C1O	6094.1	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O[Si](C)(C)C(C)(C)C)=C5)C(O)C(O)C4O)C=C3O2)C=C1O	6092.7	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OC1=CC(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O[Si](C)(C)C(C)(C)C)=C5)C(O)C(O)C4O)C=C3O2)=CC=C1O	6063.1	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC(O)=C4C(=O)CC(C5=CC=C(O)C(O)=C5)OC4=C3)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)=CC(O)=C1O	6099.2	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC(O)=C4C(=O)CC(C5=CC=C(O)C(O)=C5)OC4=C3)C(O)C(O)C2O)=CC(O[Si](C)(C)C(C)(C)C)=C1O	6083.8	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC(O)=C4C(=O)CC(C5=CC=C(O)C(O)=C5)OC4=C3)C(O)C(O)C2O)=CC(O)=C1O[Si](C)(C)C(C)(C)C	6028.2	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC(O)=C4C(=O)CC(C5=CC=C(O)C(O)=C5)OC4=C3)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)=CC(O)=C1O	6086.6	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OC1=CC(OC2OC(COC(=O)C3=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)C(O)C(O)C2O)=CC2=C1C(=O)CC(C1=CC=C(O)C(O)=C1)O2	6078.4	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TBDMS,isomer #21	CC(C)(C)[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C5)C(O)C(O)C4O)C=C3O2)C=C1O	6087.1	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TBDMS,isomer #22	CC(C)(C)[Si](C)(C)OC1=CC(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C5)C(O)C(O)C4O)C=C3O2)=CC=C1O	6057.3	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TBDMS,isomer #23	CC(C)(C)[Si](C)(C)OC1=C(O)C=C(C(=O)OCC2OC(OC3=CC(O)=C4C(=O)CC(C5=CC=C(O)C(O)=C5)OC4=C3)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C=C1O	6089.0	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TBDMS,isomer #24	CC(C)(C)[Si](C)(C)OC1=CC(OC2OC(COC(=O)C3=CC(O)=C(O)C(O)=C3)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)=CC2=C1C(=O)CC(C1=CC=C(O)C(O)=C1)O2	6135.7	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TBDMS,isomer #25	CC(C)(C)[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O)C(O)C4O)C=C3O[Si](C)(C)C(C)(C)C)O2)C=C1O	6120.2	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TBDMS,isomer #26	CC(C)(C)[Si](C)(C)OC1=CC(C2CC(=O)C3=C(C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O)C(O)C4O)C=C3O[Si](C)(C)C(C)(C)C)O2)=CC=C1O	6098.4	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TBDMS,isomer #27	CC(C)(C)[Si](C)(C)OC1=CC(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O)C(O)C4O[Si](C)(C)C(C)(C)C)C=C3O2)=CC=C1O	6107.1	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TBDMS,isomer #28	CC(C)(C)[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O)C(O)C4O)C=C3O2)C=C1O[Si](C)(C)C(C)(C)C	6102.2	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TBDMS,isomer #29	CC(C)(C)[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O)C(O)C4O[Si](C)(C)C(C)(C)C)C=C3O2)C=C1O	6135.0	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC1=C(O)C=C(C(=O)OCC2OC(OC3=CC(O)=C4C(=O)CC(C5=CC=C(O)C(O)=C5)OC4=C3)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C=C1O	6097.2	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC1=CC(OC2OC(COC(=O)C3=CC(O)=C(O)C(O)=C3)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)=CC2=C1C(=O)CC(C1=CC=C(O)C(O)=C1)O2	6137.1	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC1=CC=C(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O)C(O[Si](C)(C)C(C)(C)C)C4O)C=C3O2)C=C1O	6125.1	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC1=CC(C2CC(=O)C3=C(O)C=C(OC4OC(COC(=O)C5=CC(O)=C(O)C(O)=C5)C(O)C(O[Si](C)(C)C(C)(C)C)C4O)C=C3O2)=CC=C1O	6088.9	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC1C(OC2=CC(O)=C3C(=O)CC(C4=CC=C(O)C(O)=C4)OC3=C2)OC(COC(=O)C2=CC(O)=C(O)C(O)=C2)C(O)C1O[Si](C)(C)C(C)(C)C	6161.1	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC1=CC(C(=O)OCC2OC(OC3=CC(O)=C4C(=O)CC(C5=CC=C(O)C(O)=C5)OC4=C3)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)=CC(O)=C1O	6071.0	Semi standard non polar	33892256
Eriodictyol 7-(6-galloylglucoside),2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC1=C(O)C=C(C(=O)OCC2OC(OC3=CC(O)=C4C(=O)CC(C5=CC=C(O)C(O)=C5)OC4=C3)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C=C1O	6067.9	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 - Eriodictyol 7-(6-galloylglucoside) GC-MS (Non-derivatized) - 70eV, Positive	splash10-0udr-4983320000-8e83c0f77a252e33f053	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eriodictyol 7-(6-galloylglucoside) GC-MS (1 TMS) - 70eV, Positive	splash10-0udi-3944212000-3cf57dc32d2647964c54	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eriodictyol 7-(6-galloylglucoside) GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eriodictyol 7-(6-galloylglucoside) GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eriodictyol 7-(6-galloylglucoside) GC-MS (TMS_1_4) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eriodictyol 7-(6-galloylglucoside) GC-MS (TMS_1_5) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eriodictyol 7-(6-galloylglucoside) GC-MS (TMS_1_6) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eriodictyol 7-(6-galloylglucoside) GC-MS (TMS_1_7) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eriodictyol 7-(6-galloylglucoside) GC-MS (TMS_1_8) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eriodictyol 7-(6-galloylglucoside) GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eriodictyol 7-(6-galloylglucoside) GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eriodictyol 7-(6-galloylglucoside) GC-MS (TMS_2_3) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eriodictyol 7-(6-galloylglucoside) GC-MS (TMS_2_4) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eriodictyol 7-(6-galloylglucoside) GC-MS (TMS_2_5) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eriodictyol 7-(6-galloylglucoside) GC-MS (TMS_2_6) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eriodictyol 7-(6-galloylglucoside) GC-MS (TMS_2_7) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eriodictyol 7-(6-galloylglucoside) GC-MS (TMS_2_8) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eriodictyol 7-(6-galloylglucoside) GC-MS (TMS_2_9) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eriodictyol 7-(6-galloylglucoside) GC-MS (TMS_2_10) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eriodictyol 7-(6-galloylglucoside) GC-MS (TMS_2_11) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eriodictyol 7-(6-galloylglucoside) GC-MS (TMS_2_12) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eriodictyol 7-(6-galloylglucoside) GC-MS (TMS_2_13) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eriodictyol 7-(6-galloylglucoside) GC-MS (TMS_2_14) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eriodictyol 7-(6-galloylglucoside) GC-MS (TMS_2_15) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eriodictyol 7-(6-galloylglucoside) GC-MS (TMS_2_16) - 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 - Eriodictyol 7-(6-galloylglucoside) 10V, Positive-QTOF	splash10-0f79-0590322000-42cb13ef8d08edc32196	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Eriodictyol 7-(6-galloylglucoside) 20V, Positive-QTOF	splash10-000i-0590000000-285e97681ca771dd3aa7	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Eriodictyol 7-(6-galloylglucoside) 40V, Positive-QTOF	splash10-0uei-0920000000-30809a3b2d4a4f7913ba	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Eriodictyol 7-(6-galloylglucoside) 10V, Negative-QTOF	splash10-0gbi-0951104000-76f7fa0574b762a2e34e	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Eriodictyol 7-(6-galloylglucoside) 20V, Negative-QTOF	splash10-014r-0960000000-2cab22ea53afb578801c	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Eriodictyol 7-(6-galloylglucoside) 40V, Negative-QTOF	splash10-014r-0960000000-3ee2fc68e98777cb362d	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Eriodictyol 7-(6-galloylglucoside) 10V, Negative-QTOF	splash10-0udi-0000009000-a2fca8344c8471829cbb	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Eriodictyol 7-(6-galloylglucoside) 20V, Negative-QTOF	splash10-0uxr-0000908000-5244a17b051f6ca0f657	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Eriodictyol 7-(6-galloylglucoside) 40V, Negative-QTOF	splash10-000i-0900400000-308f815cb9bae2939444	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Eriodictyol 7-(6-galloylglucoside) 10V, Positive-QTOF	splash10-0udi-0000009000-53e4bf4dd62840138750	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Eriodictyol 7-(6-galloylglucoside) 20V, Positive-QTOF	splash10-0gba-0400906000-c3fa0a71789cfc84241f	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Eriodictyol 7-(6-galloylglucoside) 40V, Positive-QTOF	splash10-014i-0300900000-ddb987005ad51146bf4b	2021-09-23	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Cytoplasm
Extracellular

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB019583

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

74819398

PDB ID

Not Available

ChEBI ID

176251

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

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

Showing metabocard for Eriodictyol 7-(6-galloylglucoside) (HMDB0039921)

MOL for HMDB0039921 (Eriodictyol 7-(6-galloylglucoside))

3D MOL for HMDB0039921 (Eriodictyol 7-(6-galloylglucoside))

3D SDF for HMDB0039921 (Eriodictyol 7-(6-galloylglucoside))

3D-SDF for HMDB0039921 (Eriodictyol 7-(6-galloylglucoside))

PDB for HMDB0039921 (Eriodictyol 7-(6-galloylglucoside))

3D PDB for HMDB0039921 (Eriodictyol 7-(6-galloylglucoside))

SMILES for HMDB0039921 (Eriodictyol 7-(6-galloylglucoside))

INCHI for HMDB0039921 (Eriodictyol 7-(6-galloylglucoside))

Structure for HMDB0039921 (Eriodictyol 7-(6-galloylglucoside))

3D Structure for HMDB0039921 (Eriodictyol 7-(6-galloylglucoside))

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra