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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2017-09-18 01:38:39 UTC

Update Date

2021-09-14 15:16:47 UTC

HMDB ID

HMDB0134110

Secondary Accession Numbers

None

Metabolite Identification

Common Name

6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid

Description

6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose. Based on a literature review very few articles have been published on 6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid.

Structure

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

HMDB0134110
     RDKit          3D
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid
 37 38  0  0  0  0  0  0  0  0999 V2000
   -2.4294   -2.2309    0.3893 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3409   -1.4974   -0.0459 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6267   -1.9910   -0.0943 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0437   -0.1598   -0.4875 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0674    0.6333   -0.9650 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7806    1.9143   -1.3877 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8312    2.6891   -1.8633 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4862    2.3707   -1.3240 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4365    1.5907   -0.8466 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7282    0.3114   -0.4254 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7920   -0.5637    0.0667 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5487   -0.2837    0.2036 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9254   -0.4525    1.5418 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2615   -0.2444    1.7710 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4518    0.9230    2.6575 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4469    1.5430    3.0678 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7020    1.3595    3.0535 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0692    0.0178    0.5190 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4205   -0.0654    0.8544 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7697   -0.9473   -0.5893 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5003   -2.1198   -0.4977 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3046   -1.3103   -0.6584 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7987   -1.2156   -1.9328 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7846   -2.9542   -0.3820 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0806    0.2140   -0.9918 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3190    3.2528   -1.1552 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2386    3.3626   -1.6467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4372    2.0007   -0.8188 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8834    0.7105   -0.1029 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7438   -1.1478    2.2448 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9376    1.6002    4.0067 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8759    1.0493    0.1642 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7256   -0.9786    1.0096 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0240   -0.4388   -1.5467 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5752   -2.5736   -1.3727 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0841   -2.2950   -0.2125 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3740   -2.0733   -2.2029 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  2  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  1  0
  6  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 14 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 10  4  1  0
 22 12  1  0
  3 24  1  0
  5 25  1  0
  7 26  1  0
  8 27  1  0
  9 28  1  0
 12 29  1  0
 14 30  1  0
 17 31  1  0
 18 32  1  0
 19 33  1  0
 20 34  1  0
 21 35  1  0
 22 36  1  0
 23 37  1  0
M  END


  Mrv1652308221920372D          

 23 24  0  0  0  0            999 V2000
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    7.0125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  2  0  0  0  0
  4  1  1  0  0  0  0
  4  3  2  0  0  0  0
  5  3  1  0  0  0  0
  6  2  1  0  0  0  0
  6  5  2  0  0  0  0
  8  7  1  0  0  0  0
  9  7  1  0  0  0  0
 10  8  1  0  0  0  0
 11  5  1  0  0  0  0
 12 10  1  0  0  0  0
 13  9  1  0  0  0  0
 14  4  1  0  0  0  0
 15  7  1  0  0  0  0
 16  8  1  0  0  0  0
 17  9  1  0  0  0  0
 18 11  2  0  0  0  0
 19 11  1  0  0  0  0
 20 12  2  0  0  0  0
 21 12  1  0  0  0  0
 22  6  1  0  0  0  0
 22 13  1  0  0  0  0
 23 10  1  0  0  0  0
 23 13  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0134110

> <DATABASE_NAME>
hmdb

> <SMILES>
OC1C(O)C(OC2=C(C=C(O)C=C2)C(O)=O)OC(C1O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C13H14O10/c14-4-1-2-6(5(3-4)11(18)19)22-13-9(17)7(15)8(16)10(23-13)12(20)21/h1-3,7-10,13-17H,(H,18,19)(H,20,21)

> <INCHI_KEY>
YMTKHYRBSOTLTP-UHFFFAOYSA-N

> <FORMULA>
C13H14O10

> <MOLECULAR_WEIGHT>
330.245

> <EXACT_MASS>
330.058696651

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
37

> <JCHEM_AVERAGE_POLARIZABILITY>
29.08195466042469

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid

> <ALOGPS_LOGP>
-0.19

> <JCHEM_LOGP>
-0.9240954746666665

> <ALOGPS_LOGS>
-1.32

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
3.7339845706787793

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.67772853625

> <JCHEM_PKA_STRONGEST_BASIC>
-3.686827051885045

> <JCHEM_POLAR_SURFACE_AREA>
173.98

> <JCHEM_REFRACTIVITY>
69.2878

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.57e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0134110
     RDKit          3D
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid
 37 38  0  0  0  0  0  0  0  0999 V2000
   -2.4294   -2.2309    0.3893 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3409   -1.4974   -0.0459 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6267   -1.9910   -0.0943 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0437   -0.1598   -0.4875 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0674    0.6333   -0.9650 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7806    1.9143   -1.3877 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8312    2.6891   -1.8633 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4862    2.3707   -1.3240 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4365    1.5907   -0.8466 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7282    0.3114   -0.4254 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7920   -0.5637    0.0667 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5487   -0.2837    0.2036 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9254   -0.4525    1.5418 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2615   -0.2444    1.7710 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4518    0.9230    2.6575 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4469    1.5430    3.0678 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7020    1.3595    3.0535 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0692    0.0178    0.5190 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4205   -0.0654    0.8544 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7697   -0.9473   -0.5893 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5003   -2.1198   -0.4977 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3046   -1.3103   -0.6584 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7987   -1.2156   -1.9328 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7846   -2.9542   -0.3820 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0806    0.2140   -0.9918 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3190    3.2528   -1.1552 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2386    3.3626   -1.6467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4372    2.0007   -0.8188 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8834    0.7105   -0.1029 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7438   -1.1478    2.2448 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9376    1.6002    4.0067 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8759    1.0493    0.1642 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7256   -0.9786    1.0096 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0240   -0.4388   -1.5467 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5752   -2.5736   -1.3727 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0841   -2.2950   -0.2125 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3740   -2.0733   -2.2029 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  2  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  1  0
  6  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 14 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 10  4  1  0
 22 12  1  0
  3 24  1  0
  5 25  1  0
  7 26  1  0
  8 27  1  0
  9 28  1  0
 12 29  1  0
 14 30  1  0
 17 31  1  0
 18 32  1  0
 19 33  1  0
 20 34  1  0
 21 35  1  0
 22 36  1  0
 23 37  1  0
M  END

HEADER    PROTEIN                                 22-AUG-19   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   22-AUG-19         0                                  
HETATM    1  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.667   6.160   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.335   4.620   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.335   6.160   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.001   6.930   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.334  11.550   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.000  10.780   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.667  10.780   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.000   9.240   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.668   6.930   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.334   8.470   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.667   9.240   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       4.001   2.310   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0       1.334  13.090   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0      -1.334  11.550   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       4.001  11.550   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0       8.002   6.160   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       6.668   8.470   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      -1.334   6.930   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      -2.667   9.240   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       4.001   8.470   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       1.334   8.470   0.000  0.00  0.00           O+0
CONECT    1    2    4                                                       
CONECT    2    1    6                                                       
CONECT    3    4    5                                                       
CONECT    4    1    3   14                                                  
CONECT    5    3    6   11                                                  
CONECT    6    2    5   22                                                  
CONECT    7    8    9   15                                                  
CONECT    8    7   10   16                                                  
CONECT    9    7   13   17                                                  
CONECT   10    8   12   23                                                  
CONECT   11    5   18   19                                                  
CONECT   12   10   20   21                                                  
CONECT   13    9   22   23                                                  
CONECT   14    4                                                            
CONECT   15    7                                                            
CONECT   16    8                                                            
CONECT   17    9                                                            
CONECT   18   11                                                            
CONECT   19   11                                                            
CONECT   20   12                                                            
CONECT   21   12                                                            
CONECT   22    6   13                                                       
CONECT   23   10   13                                                       
MASTER        0    0    0    0    0    0    0    0   23    0   48    0
END

COMPND    HMDB0134110
HETATM    1  O1  UNL     1      -2.429  -2.231   0.389  1.00  0.00           O  
HETATM    2  C1  UNL     1      -3.341  -1.497  -0.046  1.00  0.00           C  
HETATM    3  O2  UNL     1      -4.627  -1.991  -0.094  1.00  0.00           O  
HETATM    4  C2  UNL     1      -3.044  -0.160  -0.487  1.00  0.00           C  
HETATM    5  C3  UNL     1      -4.067   0.633  -0.965  1.00  0.00           C  
HETATM    6  C4  UNL     1      -3.781   1.914  -1.388  1.00  0.00           C  
HETATM    7  O3  UNL     1      -4.831   2.689  -1.863  1.00  0.00           O  
HETATM    8  C5  UNL     1      -2.486   2.371  -1.324  1.00  0.00           C  
HETATM    9  C6  UNL     1      -1.437   1.591  -0.847  1.00  0.00           C  
HETATM   10  C7  UNL     1      -1.728   0.311  -0.425  1.00  0.00           C  
HETATM   11  O4  UNL     1      -0.792  -0.564   0.067  1.00  0.00           O  
HETATM   12  C8  UNL     1       0.549  -0.284   0.204  1.00  0.00           C  
HETATM   13  O5  UNL     1       0.925  -0.452   1.542  1.00  0.00           O  
HETATM   14  C9  UNL     1       2.261  -0.244   1.771  1.00  0.00           C  
HETATM   15  C10 UNL     1       2.452   0.923   2.658  1.00  0.00           C  
HETATM   16  O6  UNL     1       1.447   1.543   3.068  1.00  0.00           O  
HETATM   17  O7  UNL     1       3.702   1.359   3.054  1.00  0.00           O  
HETATM   18  C11 UNL     1       3.069   0.018   0.519  1.00  0.00           C  
HETATM   19  O8  UNL     1       4.421  -0.065   0.854  1.00  0.00           O  
HETATM   20  C12 UNL     1       2.770  -0.947  -0.589  1.00  0.00           C  
HETATM   21  O9  UNL     1       3.500  -2.120  -0.498  1.00  0.00           O  
HETATM   22  C13 UNL     1       1.305  -1.310  -0.658  1.00  0.00           C  
HETATM   23  O10 UNL     1       0.799  -1.216  -1.933  1.00  0.00           O  
HETATM   24  H1  UNL     1      -4.785  -2.954  -0.382  1.00  0.00           H  
HETATM   25  H2  UNL     1      -5.081   0.214  -0.992  1.00  0.00           H  
HETATM   26  H3  UNL     1      -5.319   3.253  -1.155  1.00  0.00           H  
HETATM   27  H4  UNL     1      -2.239   3.363  -1.647  1.00  0.00           H  
HETATM   28  H5  UNL     1      -0.437   2.001  -0.819  1.00  0.00           H  
HETATM   29  H6  UNL     1       0.883   0.710  -0.103  1.00  0.00           H  
HETATM   30  H7  UNL     1       2.744  -1.148   2.245  1.00  0.00           H  
HETATM   31  H8  UNL     1       3.938   1.600   4.007  1.00  0.00           H  
HETATM   32  H9  UNL     1       2.876   1.049   0.164  1.00  0.00           H  
HETATM   33  H10 UNL     1       4.726  -0.979   1.010  1.00  0.00           H  
HETATM   34  H11 UNL     1       3.024  -0.439  -1.547  1.00  0.00           H  
HETATM   35  H12 UNL     1       3.575  -2.574  -1.373  1.00  0.00           H  
HETATM   36  H13 UNL     1       1.084  -2.295  -0.213  1.00  0.00           H  
HETATM   37  H14 UNL     1       0.374  -2.073  -2.203  1.00  0.00           H  
CONECT    1    2    2
CONECT    2    3    4
CONECT    3   24
CONECT    4    5    5   10
CONECT    5    6   25
CONECT    6    7    8    8
CONECT    7   26
CONECT    8    9   27
CONECT    9   10   10   28
CONECT   10   11
CONECT   11   12
CONECT   12   13   22   29
CONECT   13   14
CONECT   14   15   18   30
CONECT   15   16   16   17
CONECT   17   31
CONECT   18   19   20   32
CONECT   19   33
CONECT   20   21   22   34
CONECT   21   35
CONECT   22   23   36
CONECT   23   37
END

HMDB0134110
     RDKit          3D
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid
 37 38  0  0  0  0  0  0  0  0999 V2000
   -2.4294   -2.2309    0.3893 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3409   -1.4974   -0.0459 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6267   -1.9910   -0.0943 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0437   -0.1598   -0.4875 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0674    0.6333   -0.9650 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7806    1.9143   -1.3877 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8312    2.6891   -1.8633 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4862    2.3707   -1.3240 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4365    1.5907   -0.8466 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7282    0.3114   -0.4254 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7920   -0.5637    0.0667 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5487   -0.2837    0.2036 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9254   -0.4525    1.5418 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2615   -0.2444    1.7710 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4518    0.9230    2.6575 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4469    1.5430    3.0678 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7020    1.3595    3.0535 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0692    0.0178    0.5190 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4205   -0.0654    0.8544 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7697   -0.9473   -0.5893 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5003   -2.1198   -0.4977 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3046   -1.3103   -0.6584 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7987   -1.2156   -1.9328 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7846   -2.9542   -0.3820 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0806    0.2140   -0.9918 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3190    3.2528   -1.1552 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2386    3.3626   -1.6467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4372    2.0007   -0.8188 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8834    0.7105   -0.1029 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7438   -1.1478    2.2448 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9376    1.6002    4.0067 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8759    1.0493    0.1642 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7256   -0.9786    1.0096 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0240   -0.4388   -1.5467 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5752   -2.5736   -1.3727 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0841   -2.2950   -0.2125 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3740   -2.0733   -2.2029 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  2  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  1  0
  6  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 14 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 10  4  1  0
 22 12  1  0
  3 24  1  0
  5 25  1  0
  7 26  1  0
  8 27  1  0
  9 28  1  0
 12 29  1  0
 14 30  1  0
 17 31  1  0
 18 32  1  0
 19 33  1  0
 20 34  1  0
 21 35  1  0
 22 36  1  0
 23 37  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
6-(2-Carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylate	Generator

Chemical Formula

C₁₃H₁₄O₁₀

Average Molecular Weight

330.245

Monoisotopic Molecular Weight

330.058696651

IUPAC Name

6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid

Traditional Name

6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid

CAS Registry Number

Not Available

SMILES

OC1C(O)C(OC2=C(C=C(O)C=C2)C(O)=O)OC(C1O)C(O)=O

InChI Identifier

InChI=1S/C13H14O10/c14-4-1-2-6(5(3-4)11(18)19)22-13-9(17)7(15)8(16)10(23-13)12(20)21/h1-3,7-10,13-17H,(H,18,19)(H,20,21)

InChI Key

YMTKHYRBSOTLTP-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Phenolic glycosides

Alternative Parents

Substituents

Phenolic glycoside
1-o-glucuronide
O-glucuronide
Glucuronic acid or derivatives
Hexose monosaccharide
O-glycosyl compound
Hydroxybenzoic acid
4-alkoxyphenol
Benzoic acid or derivatives
Benzoic acid
Phenol ether
Phenoxy compound
Benzoyl
Phenol
1-hydroxy-2-unsubstituted benzenoid
Beta-hydroxy acid
Pyran
Dicarboxylic acid or derivatives
Oxane
Hydroxy acid
Monocyclic benzene moiety
Monosaccharide
Benzenoid
Secondary alcohol
Carboxylic acid
Carboxylic acid derivative
Acetal
Organoheterocyclic compound
Oxacycle
Polyol
Carbonyl group
Hydrocarbon derivative
Organic oxide
Alcohol
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 32966057)

Excreta

Biofluid or Excreta

Urine (PMID: 32966057)

Source

Endogenous

Endogenous (HMDB: HMDB0134110)

Exogenous

Food

Cocoa and cocoa product

Cocoa and cocoa products (HMDB: HMDB0134110)

Coffee and coffee product

Coffee product

Coffee products (HMDB: HMDB0134110)

Tea

Tea products (HMDB: HMDB0134110)

Fat and oil

Olive oil (HMDB: HMDB0134110)

Fruit

Fruits (HMDB: HMDB0134110)

Vegetable

Vegetables (HMDB: HMDB0134110)

Legumes (HMDB: HMDB0134110)

Cereal and cereal product

Cereal product

Whole grain cereal products (HMDB: HMDB0134110)

Nut

Nuts (HMDB: HMDB0134110)

Beverage

Alcoholic beverage

Red wine (HMDB: HMDB0134110)

Process

Not Available

Role

Not Available

Physical Properties

State

Not Available

Experimental Molecular Properties

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

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	-0.19	ALOGPS
logP	-0.92	ChemAxon
logS	-1.3	ALOGPS
pKa (Strongest Acidic)	2.68	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	173.98 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	69.29 m³·mol⁻¹	ChemAxon
Polarizability	29.08 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	175.002	31661259
DarkChem	[M-H]-	170.796	31661259
DeepCCS	[M+H]+	168.744	30932474
DeepCCS	[M-H]-	166.386	30932474
DeepCCS	[M-2H]-	199.371	30932474
DeepCCS	[M+Na]+	174.837	30932474
AllCCS	[M+H]+	173.7	32859911
AllCCS	[M+H-H2O]+	170.6	32859911
AllCCS	[M+NH4]+	176.6	32859911
AllCCS	[M+Na]+	177.5	32859911
AllCCS	[M-H]-	168.6	32859911
AllCCS	[M+Na-2H]-	168.3	32859911
AllCCS	[M+HCOO]-	168.1	32859911

Predicted Retention Times

Underivatized

Chromatographic Method	Retention Time	Reference
Measured using a Waters Acquity ultraperformance liquid chromatography (UPLC) ethylene-bridged hybrid (BEH) C18 column (100 mm × 2.1 mm; 1.7 μmparticle diameter). Predicted by Afia on May 17, 2022.	2.97 minutes	32390414
Predicted by Siyang on May 30, 2022	10.7351 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	7.75 minutes	32390414
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	895.3 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	250.6 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	58.8 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	166.2 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	68.6 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	268.8 seconds	40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid	277.5 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	677.0 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	592.4 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	152.2 seconds	40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid	1046.8 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	205.3 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	197.1 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	541.4 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	314.2 seconds	40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water	380.1 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid	OC1C(O)C(OC2=C(C=C(O)C=C2)C(O)=O)OC(C1O)C(O)=O	4554.1	Standard polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid	OC1C(O)C(OC2=C(C=C(O)C=C2)C(O)=O)OC(C1O)C(O)=O	3020.9	Standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid	OC1C(O)C(OC2=C(C=C(O)C=C2)C(O)=O)OC(C1O)C(O)=O	3034.2	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,1TMS,isomer #1	C[Si](C)(C)OC1C(O)C(OC2=CC=C(O)C=C2C(=O)O)OC(C(=O)O)C1O	3044.7	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,1TMS,isomer #2	C[Si](C)(C)OC1C(OC2=CC=C(O)C=C2C(=O)O)OC(C(=O)O)C(O)C1O	3041.1	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,1TMS,isomer #3	C[Si](C)(C)OC1=CC=C(OC2OC(C(=O)O)C(O)C(O)C2O)C(C(=O)O)=C1	3068.7	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,1TMS,isomer #4	C[Si](C)(C)OC(=O)C1=CC(O)=CC=C1OC1OC(C(=O)O)C(O)C(O)C1O	3036.4	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,1TMS,isomer #5	C[Si](C)(C)OC1C(C(=O)O)OC(OC2=CC=C(O)C=C2C(=O)O)C(O)C1O	3038.3	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,1TMS,isomer #6	C[Si](C)(C)OC(=O)C1OC(OC2=CC=C(O)C=C2C(=O)O)C(O)C(O)C1O	3032.2	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,2TMS,isomer #1	C[Si](C)(C)OC1C(OC2=CC=C(O)C=C2C(=O)O)OC(C(=O)O)C(O)C1O[Si](C)(C)C	3033.6	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,2TMS,isomer #10	C[Si](C)(C)OC(=O)C1OC(OC2=CC=C(O[Si](C)(C)C)C=C2C(=O)O)C(O)C(O)C1O	2985.1	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,2TMS,isomer #11	C[Si](C)(C)OC1=CC=C(OC2OC(C(=O)O)C(O[Si](C)(C)C)C(O)C2O)C(C(=O)O)=C1	3004.4	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,2TMS,isomer #12	C[Si](C)(C)OC(=O)C1=CC(O[Si](C)(C)C)=CC=C1OC1OC(C(=O)O)C(O)C(O)C1O	2972.5	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,2TMS,isomer #13	C[Si](C)(C)OC(=O)C1=CC(O)=CC=C1OC1OC(C(=O)O[Si](C)(C)C)C(O)C(O)C1O	2978.9	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,2TMS,isomer #14	C[Si](C)(C)OC(=O)C1=CC(O)=CC=C1OC1OC(C(=O)O)C(O[Si](C)(C)C)C(O)C1O	2969.8	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,2TMS,isomer #15	C[Si](C)(C)OC(=O)C1OC(OC2=CC=C(O)C=C2C(=O)O)C(O)C(O)C1O[Si](C)(C)C	2992.6	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,2TMS,isomer #2	C[Si](C)(C)OC1=CC=C(OC2OC(C(=O)O)C(O)C(O[Si](C)(C)C)C2O)C(C(=O)O)=C1	2995.1	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,2TMS,isomer #3	C[Si](C)(C)OC(=O)C1=CC(O)=CC=C1OC1OC(C(=O)O)C(O)C(O[Si](C)(C)C)C1O	2959.9	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,2TMS,isomer #4	C[Si](C)(C)OC(=O)C1OC(OC2=CC=C(O)C=C2C(=O)O)C(O)C(O[Si](C)(C)C)C1O	3003.3	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,2TMS,isomer #5	C[Si](C)(C)OC1C(C(=O)O)OC(OC2=CC=C(O)C=C2C(=O)O)C(O)C1O[Si](C)(C)C	3031.5	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,2TMS,isomer #6	C[Si](C)(C)OC1=CC=C(OC2OC(C(=O)O)C(O)C(O)C2O[Si](C)(C)C)C(C(=O)O)=C1	3013.2	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,2TMS,isomer #7	C[Si](C)(C)OC(=O)C1=CC(O)=CC=C1OC1OC(C(=O)O)C(O)C(O)C1O[Si](C)(C)C	2982.3	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,2TMS,isomer #8	C[Si](C)(C)OC(=O)C1OC(OC2=CC=C(O)C=C2C(=O)O)C(O[Si](C)(C)C)C(O)C1O	3011.4	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,2TMS,isomer #9	C[Si](C)(C)OC1C(OC2=CC=C(O)C=C2C(=O)O)OC(C(=O)O)C(O[Si](C)(C)C)C1O	3029.1	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,3TMS,isomer #1	C[Si](C)(C)OC1=CC=C(OC2OC(C(=O)O)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(C(=O)O)=C1	2980.6	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,3TMS,isomer #10	C[Si](C)(C)OC(=O)C1OC(OC2=CC=C(O)C=C2C(=O)O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2981.7	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,3TMS,isomer #11	C[Si](C)(C)OC(=O)C1OC(OC2=CC=C(O[Si](C)(C)C)C=C2C(=O)O)C(O[Si](C)(C)C)C(O)C1O	2950.3	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,3TMS,isomer #12	C[Si](C)(C)OC1=CC=C(OC2OC(C(=O)O)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(C(=O)O)=C1	2983.0	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,3TMS,isomer #13	C[Si](C)(C)OC(=O)C1=CC(O[Si](C)(C)C)=CC=C1OC1OC(C(=O)O)C(O)C(O)C1O[Si](C)(C)C	2905.2	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,3TMS,isomer #14	C[Si](C)(C)OC(=O)C1=CC(O)=CC=C1OC1OC(C(=O)O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C	2908.6	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,3TMS,isomer #15	C[Si](C)(C)OC(=O)C1=CC(O)=CC=C1OC1OC(C(=O)O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2948.9	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,3TMS,isomer #16	C[Si](C)(C)OC(=O)C1OC(OC2=CC=C(O)C=C2C(=O)O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2999.0	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,3TMS,isomer #17	C[Si](C)(C)OC(=O)C1=CC(O[Si](C)(C)C)=CC=C1OC1OC(C(=O)O[Si](C)(C)C)C(O)C(O)C1O	2871.0	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,3TMS,isomer #18	C[Si](C)(C)OC(=O)C1OC(OC2=CC=C(O[Si](C)(C)C)C=C2C(=O)O)C(O)C(O)C1O[Si](C)(C)C	2938.0	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,3TMS,isomer #19	C[Si](C)(C)OC(=O)C1=CC(O[Si](C)(C)C)=CC=C1OC1OC(C(=O)O)C(O[Si](C)(C)C)C(O)C1O	2895.9	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,3TMS,isomer #2	C[Si](C)(C)OC(=O)C1=CC(O)=CC=C1OC1OC(C(=O)O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2925.9	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,3TMS,isomer #20	C[Si](C)(C)OC(=O)C1=CC(O)=CC=C1OC1OC(C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O	2893.6	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,3TMS,isomer #3	C[Si](C)(C)OC(=O)C1OC(OC2=CC=C(O)C=C2C(=O)O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2994.9	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,3TMS,isomer #4	C[Si](C)(C)OC1C(OC2=CC=C(O)C=C2C(=O)O)OC(C(=O)O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3031.3	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,3TMS,isomer #5	C[Si](C)(C)OC(=O)C1OC(OC2=CC=C(O[Si](C)(C)C)C=C2C(=O)O)C(O)C(O[Si](C)(C)C)C1O	2924.5	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,3TMS,isomer #6	C[Si](C)(C)OC1=CC=C(OC2OC(C(=O)O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(C(=O)O)=C1	2969.9	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,3TMS,isomer #7	C[Si](C)(C)OC(=O)C1=CC(O[Si](C)(C)C)=CC=C1OC1OC(C(=O)O)C(O)C(O[Si](C)(C)C)C1O	2888.0	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,3TMS,isomer #8	C[Si](C)(C)OC(=O)C1=CC(O)=CC=C1OC1OC(C(=O)O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O	2858.1	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,3TMS,isomer #9	C[Si](C)(C)OC(=O)C1=CC(O)=CC=C1OC1OC(C(=O)O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2922.4	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,4TMS,isomer #1	C[Si](C)(C)OC(=O)C1OC(OC2=CC=C(O[Si](C)(C)C)C=C2C(=O)O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2946.8	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,4TMS,isomer #10	C[Si](C)(C)OC(=O)C1=CC(O)=CC=C1OC1OC(C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2853.3	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,4TMS,isomer #11	C[Si](C)(C)OC(=O)C1=CC(O[Si](C)(C)C)=CC=C1OC1OC(C(=O)O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C	2852.8	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,4TMS,isomer #12	C[Si](C)(C)OC(=O)C1OC(OC2=CC=C(O[Si](C)(C)C)C=C2C(=O)O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2958.9	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,4TMS,isomer #13	C[Si](C)(C)OC(=O)C1=CC(O[Si](C)(C)C)=CC=C1OC1OC(C(=O)O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2912.0	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,4TMS,isomer #14	C[Si](C)(C)OC(=O)C1=CC(O)=CC=C1OC1OC(C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2905.6	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,4TMS,isomer #15	C[Si](C)(C)OC(=O)C1=CC(O[Si](C)(C)C)=CC=C1OC1OC(C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O	2847.3	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,4TMS,isomer #2	C[Si](C)(C)OC1=CC=C(OC2OC(C(=O)O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(C(=O)O)=C1	2981.3	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,4TMS,isomer #3	C[Si](C)(C)OC(=O)C1=CC(O[Si](C)(C)C)=CC=C1OC1OC(C(=O)O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2889.2	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,4TMS,isomer #4	C[Si](C)(C)OC(=O)C1=CC(O)=CC=C1OC1OC(C(=O)O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2869.1	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,4TMS,isomer #5	C[Si](C)(C)OC(=O)C1=CC(O)=CC=C1OC1OC(C(=O)O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2925.0	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,4TMS,isomer #6	C[Si](C)(C)OC(=O)C1OC(OC2=CC=C(O)C=C2C(=O)O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2997.8	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,4TMS,isomer #7	C[Si](C)(C)OC(=O)C1=CC(O[Si](C)(C)C)=CC=C1OC1OC(C(=O)O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O	2837.2	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,4TMS,isomer #8	C[Si](C)(C)OC(=O)C1OC(OC2=CC=C(O[Si](C)(C)C)C=C2C(=O)O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2935.1	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,4TMS,isomer #9	C[Si](C)(C)OC(=O)C1=CC(O[Si](C)(C)C)=CC=C1OC1OC(C(=O)O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2891.2	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,5TMS,isomer #1	C[Si](C)(C)OC(=O)C1=CC(O[Si](C)(C)C)=CC=C1OC1OC(C(=O)O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2871.7	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,5TMS,isomer #2	C[Si](C)(C)OC(=O)C1OC(OC2=CC=C(O[Si](C)(C)C)C=C2C(=O)O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2957.1	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,5TMS,isomer #3	C[Si](C)(C)OC(=O)C1=CC(O[Si](C)(C)C)=CC=C1OC1OC(C(=O)O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2896.8	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,5TMS,isomer #4	C[Si](C)(C)OC(=O)C1=CC(O)=CC=C1OC1OC(C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2899.5	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,5TMS,isomer #5	C[Si](C)(C)OC(=O)C1=CC(O[Si](C)(C)C)=CC=C1OC1OC(C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2866.5	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,5TMS,isomer #6	C[Si](C)(C)OC(=O)C1=CC(O[Si](C)(C)C)=CC=C1OC1OC(C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2895.7	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,6TMS,isomer #1	C[Si](C)(C)OC(=O)C1=CC(O[Si](C)(C)C)=CC=C1OC1OC(C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2896.4	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC1C(O)C(OC2=CC=C(O)C=C2C(=O)O)OC(C(=O)O)C1O	3317.6	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1C(OC2=CC=C(O)C=C2C(=O)O)OC(C(=O)O)C(O)C1O	3317.4	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC1=CC=C(OC2OC(C(=O)O)C(O)C(O)C2O)C(C(=O)O)=C1	3325.5	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC(=O)C1=CC(O)=CC=C1OC1OC(C(=O)O)C(O)C(O)C1O	3308.0	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC1C(C(=O)O)OC(OC2=CC=C(O)C=C2C(=O)O)C(O)C1O	3301.6	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,1TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC(=O)C1OC(OC2=CC=C(O)C=C2C(=O)O)C(O)C(O)C1O	3308.7	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC1C(OC2=CC=C(O)C=C2C(=O)O)OC(C(=O)O)C(O)C1O[Si](C)(C)C(C)(C)C	3496.9	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC(=O)C1OC(OC2=CC=C(O[Si](C)(C)C(C)(C)C)C=C2C(=O)O)C(O)C(O)C1O	3447.0	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC1=CC=C(OC2OC(C(=O)O)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C(C(=O)O)=C1	3446.4	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC(=O)C1=CC(O[Si](C)(C)C(C)(C)C)=CC=C1OC1OC(C(=O)O)C(O)C(O)C1O	3443.0	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,2TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC(=O)C1=CC(O)=CC=C1OC1OC(C(=O)O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O	3406.9	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,2TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC(=O)C1=CC(O)=CC=C1OC1OC(C(=O)O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	3406.1	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,2TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC(=O)C1OC(OC2=CC=C(O)C=C2C(=O)O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	3459.5	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1=CC=C(OC2OC(C(=O)O)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C(C(=O)O)=C1	3467.3	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC(=O)C1=CC(O)=CC=C1OC1OC(C(=O)O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	3414.4	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC(=O)C1OC(OC2=CC=C(O)C=C2C(=O)O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	3455.1	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC1C(C(=O)O)OC(OC2=CC=C(O)C=C2C(=O)O)C(O)C1O[Si](C)(C)C(C)(C)C	3475.8	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC1=CC=C(OC2OC(C(=O)O)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C(C(=O)O)=C1	3473.0	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC(=O)C1=CC(O)=CC=C1OC1OC(C(=O)O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	3427.8	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC(=O)C1OC(OC2=CC=C(O)C=C2C(=O)O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	3470.4	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC1C(OC2=CC=C(O)C=C2C(=O)O)OC(C(=O)O)C(O[Si](C)(C)C(C)(C)C)C1O	3487.5	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC1=CC=C(OC2OC(C(=O)O)C(O)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C(C(=O)O)=C1	3628.0	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC(=O)C1OC(OC2=CC=C(O)C=C2C(=O)O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3590.9	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC(=O)C1OC(OC2=CC=C(O[Si](C)(C)C(C)(C)C)C=C2C(=O)O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	3598.9	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC1=CC=C(OC2OC(C(=O)O)C(O[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)C(C(=O)O)=C1	3618.7	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC(=O)C1=CC(O[Si](C)(C)C(C)(C)C)=CC=C1OC1OC(C(=O)O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	3586.7	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC(=O)C1=CC(O)=CC=C1OC1OC(C(=O)O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	3520.7	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC(=O)C1=CC(O)=CC=C1OC1OC(C(=O)O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3541.0	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OC(=O)C1OC(OC2=CC=C(O)C=C2C(=O)O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3619.5	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OC(=O)C1=CC(O[Si](C)(C)C(C)(C)C)=CC=C1OC1OC(C(=O)O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O	3553.3	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OC(=O)C1OC(OC2=CC=C(O[Si](C)(C)C(C)(C)C)C=C2C(=O)O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	3595.0	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,3TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OC(=O)C1=CC(O[Si](C)(C)C(C)(C)C)=CC=C1OC1OC(C(=O)O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	3575.9	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC(=O)C1=CC(O)=CC=C1OC1OC(C(=O)O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3544.1	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,3TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OC(=O)C1=CC(O)=CC=C1OC1OC(C(=O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	3510.7	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC(=O)C1OC(OC2=CC=C(O)C=C2C(=O)O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3603.5	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC1C(OC2=CC=C(O)C=C2C(=O)O)OC(C(=O)O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3617.6	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC(=O)C1OC(OC2=CC=C(O[Si](C)(C)C(C)(C)C)C=C2C(=O)O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	3602.4	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC1=CC=C(OC2OC(C(=O)O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)C(C(=O)O)=C1	3603.4	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC(=O)C1=CC(O[Si](C)(C)C(C)(C)C)=CC=C1OC1OC(C(=O)O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	3607.8	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC(=O)C1=CC(O)=CC=C1OC1OC(C(=O)O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	3519.3	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC(=O)C1=CC(O)=CC=C1OC1OC(C(=O)O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3528.3	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)C1OC(OC2=CC=C(O[Si](C)(C)C(C)(C)C)C=C2C(=O)O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3763.1	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC(=O)C1=CC(O)=CC=C1OC1OC(C(=O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3678.6	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC(=O)C1=CC(O[Si](C)(C)C(C)(C)C)=CC=C1OC1OC(C(=O)O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	3708.7	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,4TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC(=O)C1OC(OC2=CC=C(O[Si](C)(C)C(C)(C)C)C=C2C(=O)O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3779.6	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,4TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC(=O)C1=CC(O[Si](C)(C)C(C)(C)C)=CC=C1OC1OC(C(=O)O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3743.3	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,4TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC(=O)C1=CC(O)=CC=C1OC1OC(C(=O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3699.5	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,4TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC(=O)C1=CC(O[Si](C)(C)C(C)(C)C)=CC=C1OC1OC(C(=O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	3711.7	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1=CC=C(OC2OC(C(=O)O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C(C(=O)O)=C1	3762.4	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC(=O)C1=CC(O[Si](C)(C)C(C)(C)C)=CC=C1OC1OC(C(=O)O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3745.7	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC(=O)C1=CC(O)=CC=C1OC1OC(C(=O)O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3675.8	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC(=O)C1=CC(O)=CC=C1OC1OC(C(=O)O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3666.7	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC(=O)C1OC(OC2=CC=C(O)C=C2C(=O)O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3738.3	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC(=O)C1=CC(O[Si](C)(C)C(C)(C)C)=CC=C1OC1OC(C(=O)O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	3726.6	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC(=O)C1OC(OC2=CC=C(O[Si](C)(C)C(C)(C)C)C=C2C(=O)O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3758.6	Semi standard non polar	33892256
6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC(=O)C1=CC(O[Si](C)(C)C(C)(C)C)=CC=C1OC1OC(C(=O)O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3742.7	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid GC-MS (5 TMS) - 70eV, Positive	splash10-004i-1220019000-a6a6a097cf6732c6f27f	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid GC-MS (Non-derivatized) - 70eV, Positive	splash10-08fr-9442000000-0b71cf51d8bb7b33c7f3	2017-11-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid 10V, Positive-QTOF	splash10-0bt9-0839000000-0c6afda3acc434b23ec2	2019-02-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid 20V, Positive-QTOF	splash10-0a4r-0900000000-6968216762a4fb4b92c0	2019-02-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid 40V, Positive-QTOF	splash10-0a4r-2900000000-e504562bd2e10a3eb4b3	2019-02-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid 10V, Negative-QTOF	splash10-0fbi-1978000000-bc4134ba737c798dfc82	2019-02-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid 20V, Negative-QTOF	splash10-0zg0-1951000000-942c246fa816e6035b6d	2019-02-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid 40V, Negative-QTOF	splash10-0pb9-2900000000-d686eb13e8382d8d9cf3	2019-02-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid 10V, Positive-QTOF	splash10-03e9-0229000000-91abb664fbea2f7ad24b	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid 20V, Positive-QTOF	splash10-000j-0962000000-fa0dfa558245b7656ef1	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid 40V, Positive-QTOF	splash10-0a4r-3900000000-b74bdff705ff3fa81a3f	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid 10V, Negative-QTOF	splash10-0nor-0629000000-b1e23e1a578638954686	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid 20V, Negative-QTOF	splash10-0pb9-3921000000-c1fafd4a5af18558e6ab	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid 40V, Negative-QTOF	splash10-0a4i-3900000000-3b530257d933de99f35f	2021-09-23	Wishart Lab	View Spectrum

NMR Spectra

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

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Blood
Urine

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Detected but not Quantified	Not Quantified	Adult (>18 years old)	Both	Normal	32966057	details
Urine	Detected but not Quantified	Not Quantified	Adult (>18 years old)	Both	Normal	32966057	details

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB091126

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

131837856

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Djoumbou Feunang, Yannick (2017). Cheminformatics Tools for Enabling Metabolomics, 2017 (PhD thesis). University of Alberta.

Showing metabocard for 6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid (HMDB0134110)

MOL for HMDB0134110 (6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D MOL for HMDB0134110 (6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D SDF for HMDB0134110 (6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D-SDF for HMDB0134110 (6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid)

PDB for HMDB0134110 (6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D PDB for HMDB0134110 (6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid)

SMILES for HMDB0134110 (6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid)

INCHI for HMDB0134110 (6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid)

Structure for HMDB0134110 (6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D Structure for HMDB0134110 (6-(2-carboxy-4-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra