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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 22:07:21 UTC

Update Date

2022-03-07 02:55:07 UTC

HMDB ID

HMDB0036934

Secondary Accession Numbers

HMDB36934

Metabolite Identification

Common Name

6-Methyl 2-galloylgalactarate

Description

6-Methyl 2-galloylgalactarate belongs to the class of organic compounds known as glucuronic acid derivatives. Glucuronic acid derivatives are compounds containing a glucuronic acid moiety (or a derivative), which consists of a glucose moiety with the C6 carbon oxidized to a carboxylic acid. 6-Methyl 2-galloylgalactarate has been detected, but not quantified in, fruits. This could make 6-methyl 2-galloylgalactarate a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on 6-Methyl 2-galloylgalactarate.

Structure

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

  Mrv0541 05061309252D          

 26 26  0  0  0  0            999 V2000
    6.4302   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    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
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.0625    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
   -2.1434   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  4  2  2  0  0  0  0
  4  3  1  0  0  0  0
  5  2  1  0  0  0  0
  6  3  2  0  0  0  0
  7  5  2  0  0  0  0
  7  6  1  0  0  0  0
  9  8  1  0  0  0  0
 10  8  1  0  0  0  0
 11  9  1  0  0  0  0
 12 11  1  0  0  0  0
 13  4  1  0  0  0  0
 14 10  1  0  0  0  0
 15  5  1  0  0  0  0
 16  6  1  0  0  0  0
 17  7  1  0  0  0  0
 18  8  1  0  0  0  0
 19  9  1  0  0  0  0
 20 10  1  0  0  0  0
 21 12  2  0  0  0  0
 22 12  1  0  0  0  0
 23 13  2  0  0  0  0
 24 14  2  0  0  0  0
 25  1  1  0  0  0  0
 25 14  1  0  0  0  0
 26 11  1  0  0  0  0
 26 13  1  0  0  0  0
M  END

HMDB0036934
     RDKit          3D
6-Methyl 2-galloylgalactarate
 42 42  0  0  0  0  0  0  0  0999 V2000
   -4.6927    3.5228    0.1881 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2246    2.3455   -0.4435 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9016    1.2439    0.2975 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0300    1.3024    1.5471 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4126    0.0036   -0.3204 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3211    0.0812   -1.6972 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0235   -0.3873    0.1902 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0672   -0.4785    1.5855 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7076   -1.7094   -0.4444 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7184   -2.6073   -0.0668 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4012   -2.2988    0.0323 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6937   -1.4852   -0.2890 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5406   -0.9244    0.6594 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3093   -1.1615    1.8666 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6660   -0.0877    0.3195 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4487    0.4235    1.3212 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5306    1.2264    1.0219 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3407    1.7570    2.0306 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7785    1.4825   -0.3074 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8572    2.2865   -0.6670 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0064    0.9795   -1.3166 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2835    1.2568   -2.6475 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9305    0.1801   -1.0025 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2661   -3.6235   -0.5999 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1443   -4.4888   -0.4307 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8323   -3.9035   -1.3781 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6506    3.3278    0.7457 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8364    4.2934   -0.6020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8994    3.8971    0.8628 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0702   -0.8688   -0.0848 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7033   -0.6923   -2.1650 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2934    0.4025   -0.0844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9695   -0.7702    1.8633 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7048   -1.5930   -1.5280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7515   -2.7169    0.9100 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4281   -2.3821    1.1469 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2499    0.2182    2.3858 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1169    1.5403    2.9784 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4552    2.6802    0.0420 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0719    1.8423   -2.8730 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3376   -0.2034   -1.8262 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7686   -3.9107   -2.3907 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 13 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 17 19  2  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 21 23  2  0
 11 24  1  0
 24 25  2  0
 24 26  1  0
 23 15  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  5 30  1  0
  6 31  1  0
  7 32  1  0
  8 33  1  0
  9 34  1  0
 10 35  1  0
 11 36  1  0
 16 37  1  0
 18 38  1  0
 20 39  1  0
 22 40  1  0
 23 41  1  0
 26 42  1  0
M  END

  Mrv0541 05061309252D          

 26 26  0  0  0  0            999 V2000
    6.4302   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    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
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.0625    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
   -2.1434   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  4  2  2  0  0  0  0
  4  3  1  0  0  0  0
  5  2  1  0  0  0  0
  6  3  2  0  0  0  0
  7  5  2  0  0  0  0
  7  6  1  0  0  0  0
  9  8  1  0  0  0  0
 10  8  1  0  0  0  0
 11  9  1  0  0  0  0
 12 11  1  0  0  0  0
 13  4  1  0  0  0  0
 14 10  1  0  0  0  0
 15  5  1  0  0  0  0
 16  6  1  0  0  0  0
 17  7  1  0  0  0  0
 18  8  1  0  0  0  0
 19  9  1  0  0  0  0
 20 10  1  0  0  0  0
 21 12  2  0  0  0  0
 22 12  1  0  0  0  0
 23 13  2  0  0  0  0
 24 14  2  0  0  0  0
 25  1  1  0  0  0  0
 25 14  1  0  0  0  0
 26 11  1  0  0  0  0
 26 13  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0036934

> <DATABASE_NAME>
hmdb

> <SMILES>
COC(=O)C(O)C(O)C(O)C(OC(=O)C1=CC(O)=C(O)C(O)=C1)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C14H16O12/c1-25-14(24)10(20)8(18)9(19)11(12(21)22)26-13(23)4-2-5(15)7(17)6(16)3-4/h2-3,8-11,15-20H,1H3,(H,21,22)

> <INCHI_KEY>
UVUGMMKTRWZGRA-UHFFFAOYSA-N

> <FORMULA>
C14H16O12

> <MOLECULAR_WEIGHT>
376.2696

> <EXACT_MASS>
376.064175976

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_AVERAGE_POLARIZABILITY>
33.417305558664935

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3,4,5-trihydroxy-6-methoxy-6-oxo-2-(3,4,5-trihydroxybenzoyloxy)hexanoic acid

> <ALOGPS_LOGP>
0.49

> <JCHEM_LOGP>
-1.3589718329999996

> <ALOGPS_LOGS>
-1.75

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.106453494137533

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.7534283030985383

> <JCHEM_PKA_STRONGEST_BASIC>
-3.7315980756370957

> <JCHEM_POLAR_SURFACE_AREA>
211.27999999999997

> <JCHEM_REFRACTIVITY>
78.67219999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.62e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3,4,5-trihydroxy-6-methoxy-6-oxo-2-(3,4,5-trihydroxybenzoyloxy)hexanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0036934
     RDKit          3D
6-Methyl 2-galloylgalactarate
 42 42  0  0  0  0  0  0  0  0999 V2000
   -4.6927    3.5228    0.1881 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2246    2.3455   -0.4435 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9016    1.2439    0.2975 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0300    1.3024    1.5471 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4126    0.0036   -0.3204 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3211    0.0812   -1.6972 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0235   -0.3873    0.1902 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0672   -0.4785    1.5855 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7076   -1.7094   -0.4444 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7184   -2.6073   -0.0668 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4012   -2.2988    0.0323 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6937   -1.4852   -0.2890 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5406   -0.9244    0.6594 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3093   -1.1615    1.8666 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6660   -0.0877    0.3195 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4487    0.4235    1.3212 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5306    1.2264    1.0219 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3407    1.7570    2.0306 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7785    1.4825   -0.3074 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8572    2.2865   -0.6670 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0064    0.9795   -1.3166 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2835    1.2568   -2.6475 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9305    0.1801   -1.0025 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2661   -3.6235   -0.5999 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1443   -4.4888   -0.4307 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8323   -3.9035   -1.3781 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6506    3.3278    0.7457 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8364    4.2934   -0.6020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8994    3.8971    0.8628 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0702   -0.8688   -0.0848 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7033   -0.6923   -2.1650 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2934    0.4025   -0.0844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9695   -0.7702    1.8633 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7048   -1.5930   -1.5280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7515   -2.7169    0.9100 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4281   -2.3821    1.1469 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2499    0.2182    2.3858 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1169    1.5403    2.9784 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4552    2.6802    0.0420 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0719    1.8423   -2.8730 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3376   -0.2034   -1.8262 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7686   -3.9107   -2.3907 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 13 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 17 19  2  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 21 23  2  0
 11 24  1  0
 24 25  2  0
 24 26  1  0
 23 15  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  5 30  1  0
  6 31  1  0
  7 32  1  0
  8 33  1  0
  9 34  1  0
 10 35  1  0
 11 36  1  0
 16 37  1  0
 18 38  1  0
 20 39  1  0
 22 40  1  0
 23 41  1  0
 26 42  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      12.003  -3.850   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.334  -3.850   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.000  -1.540   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.667  -1.540   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.668  -3.850   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.002  -3.080   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.001  -3.850   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.334  -3.850   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.336  -3.850   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -4.001  -3.850   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0      -1.334   0.770   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0      -4.001  -0.770   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0       6.668  -5.390   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       5.335  -1.540   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       8.002  -1.540   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       2.667  -6.160   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       5.335  -6.160   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       1.334  -5.390   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       9.336  -5.390   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0      10.669  -3.080   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       2.667  -3.080   0.000  0.00  0.00           O+0
CONECT    1   25                                                            
CONECT    2    4    5                                                       
CONECT    3    4    6                                                       
CONECT    4    2    3   13                                                  
CONECT    5    2    7   15                                                  
CONECT    6    3    7   16                                                  
CONECT    7    5    6   17                                                  
CONECT    8    9   10   18                                                  
CONECT    9    8   11   19                                                  
CONECT   10    8   14   20                                                  
CONECT   11    9   12   26                                                  
CONECT   12   11   21   22                                                  
CONECT   13    4   23   26                                                  
CONECT   14   10   24   25                                                  
CONECT   15    5                                                            
CONECT   16    6                                                            
CONECT   17    7                                                            
CONECT   18    8                                                            
CONECT   19    9                                                            
CONECT   20   10                                                            
CONECT   21   12                                                            
CONECT   22   12                                                            
CONECT   23   13                                                            
CONECT   24   14                                                            
CONECT   25    1   14                                                       
CONECT   26   11   13                                                       
MASTER        0    0    0    0    0    0    0    0   26    0   52    0
END

COMPND    HMDB0036934
HETATM    1  C1  UNL     1      -4.693   3.523   0.188  1.00  0.00           C  
HETATM    2  O1  UNL     1      -4.225   2.345  -0.444  1.00  0.00           O  
HETATM    3  C2  UNL     1      -3.902   1.244   0.297  1.00  0.00           C  
HETATM    4  O2  UNL     1      -4.030   1.302   1.547  1.00  0.00           O  
HETATM    5  C3  UNL     1      -3.413   0.004  -0.320  1.00  0.00           C  
HETATM    6  O3  UNL     1      -3.321   0.081  -1.697  1.00  0.00           O  
HETATM    7  C4  UNL     1      -2.023  -0.387   0.190  1.00  0.00           C  
HETATM    8  O4  UNL     1      -2.067  -0.478   1.586  1.00  0.00           O  
HETATM    9  C5  UNL     1      -1.708  -1.709  -0.444  1.00  0.00           C  
HETATM   10  O5  UNL     1      -2.718  -2.607  -0.067  1.00  0.00           O  
HETATM   11  C6  UNL     1      -0.401  -2.299   0.032  1.00  0.00           C  
HETATM   12  O6  UNL     1       0.694  -1.485  -0.289  1.00  0.00           O  
HETATM   13  C7  UNL     1       1.541  -0.924   0.659  1.00  0.00           C  
HETATM   14  O7  UNL     1       1.309  -1.162   1.867  1.00  0.00           O  
HETATM   15  C8  UNL     1       2.666  -0.088   0.320  1.00  0.00           C  
HETATM   16  C9  UNL     1       3.449   0.423   1.321  1.00  0.00           C  
HETATM   17  C10 UNL     1       4.531   1.226   1.022  1.00  0.00           C  
HETATM   18  O8  UNL     1       5.341   1.757   2.031  1.00  0.00           O  
HETATM   19  C11 UNL     1       4.779   1.482  -0.307  1.00  0.00           C  
HETATM   20  O9  UNL     1       5.857   2.286  -0.667  1.00  0.00           O  
HETATM   21  C12 UNL     1       4.006   0.979  -1.317  1.00  0.00           C  
HETATM   22  O10 UNL     1       4.283   1.257  -2.647  1.00  0.00           O  
HETATM   23  C13 UNL     1       2.930   0.180  -1.002  1.00  0.00           C  
HETATM   24  C14 UNL     1      -0.266  -3.623  -0.600  1.00  0.00           C  
HETATM   25  O11 UNL     1      -1.144  -4.489  -0.431  1.00  0.00           O  
HETATM   26  O12 UNL     1       0.832  -3.903  -1.378  1.00  0.00           O  
HETATM   27  H1  UNL     1      -5.651   3.328   0.746  1.00  0.00           H  
HETATM   28  H2  UNL     1      -4.836   4.293  -0.602  1.00  0.00           H  
HETATM   29  H3  UNL     1      -3.899   3.897   0.863  1.00  0.00           H  
HETATM   30  H4  UNL     1      -4.070  -0.869  -0.085  1.00  0.00           H  
HETATM   31  H5  UNL     1      -3.703  -0.692  -2.165  1.00  0.00           H  
HETATM   32  H6  UNL     1      -1.293   0.402  -0.084  1.00  0.00           H  
HETATM   33  H7  UNL     1      -2.969  -0.770   1.863  1.00  0.00           H  
HETATM   34  H8  UNL     1      -1.705  -1.593  -1.528  1.00  0.00           H  
HETATM   35  H9  UNL     1      -2.752  -2.717   0.910  1.00  0.00           H  
HETATM   36  H10 UNL     1      -0.428  -2.382   1.147  1.00  0.00           H  
HETATM   37  H11 UNL     1       3.250   0.218   2.386  1.00  0.00           H  
HETATM   38  H12 UNL     1       5.117   1.540   2.978  1.00  0.00           H  
HETATM   39  H13 UNL     1       6.455   2.680   0.042  1.00  0.00           H  
HETATM   40  H14 UNL     1       5.072   1.842  -2.873  1.00  0.00           H  
HETATM   41  H15 UNL     1       2.338  -0.203  -1.826  1.00  0.00           H  
HETATM   42  H16 UNL     1       0.769  -3.911  -2.391  1.00  0.00           H  
CONECT    1    2   27   28   29
CONECT    2    3
CONECT    3    4    4    5
CONECT    5    6    7   30
CONECT    6   31
CONECT    7    8    9   32
CONECT    8   33
CONECT    9   10   11   34
CONECT   10   35
CONECT   11   12   24   36
CONECT   12   13
CONECT   13   14   14   15
CONECT   15   16   16   23
CONECT   16   17   37
CONECT   17   18   19   19
CONECT   18   38
CONECT   19   20   21
CONECT   20   39
CONECT   21   22   23   23
CONECT   22   40
CONECT   23   41
CONECT   24   25   25   26
CONECT   26   42
END

HMDB0036934
     RDKit          3D
6-Methyl 2-galloylgalactarate
 42 42  0  0  0  0  0  0  0  0999 V2000
   -4.6927    3.5228    0.1881 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2246    2.3455   -0.4435 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9016    1.2439    0.2975 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0300    1.3024    1.5471 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4126    0.0036   -0.3204 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3211    0.0812   -1.6972 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0235   -0.3873    0.1902 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0672   -0.4785    1.5855 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7076   -1.7094   -0.4444 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7184   -2.6073   -0.0668 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4012   -2.2988    0.0323 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6937   -1.4852   -0.2890 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5406   -0.9244    0.6594 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3093   -1.1615    1.8666 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6660   -0.0877    0.3195 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4487    0.4235    1.3212 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5306    1.2264    1.0219 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3407    1.7570    2.0306 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7785    1.4825   -0.3074 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8572    2.2865   -0.6670 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0064    0.9795   -1.3166 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2835    1.2568   -2.6475 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9305    0.1801   -1.0025 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2661   -3.6235   -0.5999 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1443   -4.4888   -0.4307 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8323   -3.9035   -1.3781 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6506    3.3278    0.7457 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8364    4.2934   -0.6020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8994    3.8971    0.8628 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0702   -0.8688   -0.0848 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7033   -0.6923   -2.1650 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2934    0.4025   -0.0844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9695   -0.7702    1.8633 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7048   -1.5930   -1.5280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7515   -2.7169    0.9100 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4281   -2.3821    1.1469 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2499    0.2182    2.3858 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1169    1.5403    2.9784 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4552    2.6802    0.0420 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0719    1.8423   -2.8730 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3376   -0.2034   -1.8262 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7686   -3.9107   -2.3907 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 13 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 17 19  2  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 21 23  2  0
 11 24  1  0
 24 25  2  0
 24 26  1  0
 23 15  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  5 30  1  0
  6 31  1  0
  7 32  1  0
  8 33  1  0
  9 34  1  0
 10 35  1  0
 11 36  1  0
 16 37  1  0
 18 38  1  0
 20 39  1  0
 22 40  1  0
 23 41  1  0
 26 42  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
6-Methyl 2-galloylgalactaric acid	Generator
3,4,5-Trihydroxy-6-methoxy-6-oxo-2-(3,4,5-trihydroxybenzoyloxy)hexanoate	HMDB

Chemical Formula

C₁₄H₁₆O₁₂

Average Molecular Weight

376.2696

Monoisotopic Molecular Weight

376.064175976

IUPAC Name

3,4,5-trihydroxy-6-methoxy-6-oxo-2-(3,4,5-trihydroxybenzoyloxy)hexanoic acid

Traditional Name

3,4,5-trihydroxy-6-methoxy-6-oxo-2-(3,4,5-trihydroxybenzoyloxy)hexanoic acid

CAS Registry Number

Not Available

SMILES

COC(=O)C(O)C(O)C(O)C(OC(=O)C1=CC(O)=C(O)C(O)=C1)C(O)=O

InChI Identifier

InChI=1S/C14H16O12/c1-25-14(24)10(20)8(18)9(19)11(12(21)22)26-13(23)4-2-5(15)7(17)6(16)3-4/h2-3,8-11,15-20H,1H3,(H,21,22)

InChI Key

UVUGMMKTRWZGRA-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as glucuronic acid derivatives. Glucuronic acid derivatives are compounds containing a glucuronic acid moiety (or a derivative), which consists of a glucose moiety with the C6 carbon oxidized to a carboxylic acid.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Glucuronic acid derivatives

Alternative Parents

Substituents

Glucuronic acid or derivatives
Galloyl ester
Gallic acid or derivatives
P-hydroxybenzoic acid alkyl ester
M-hydroxybenzoic acid ester
P-hydroxybenzoic acid ester
Benzoate ester
Benzenetriol
Benzoic acid or derivatives
Pyrogallol derivative
Tricarboxylic acid or derivatives
Benzoyl
Fatty acid ester
Beta-hydroxy acid
1-hydroxy-2-unsubstituted benzenoid
Phenol
1-hydroxy-4-unsubstituted benzenoid
Monocyclic benzene moiety
Fatty acyl
Benzenoid
Monosaccharide
Hydroxy acid
Methyl ester
Carboxylic acid ester
Secondary alcohol
Carboxylic acid derivative
Carboxylic acid
Polyol
Carbonyl group
Alcohol
Organic oxide
Hydrocarbon derivative
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Extracellular (HMDB: HMDB0036934)
Cytoplasm (HMDB: HMDB0036934)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0036934)

Source

Exogenous

Exogenous (HMDB: HMDB0036934)

Food

Food (HMDB: HMDB0036934)

Fruit

Fruits (FooDB: FOOD00871)

Endogenous

Plant

Plant (HMDB: HMDB0036934)

Process

Not Available

Role

Biological role

Nutrient (HMDB: HMDB0036934)

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	6.62 g/L	ALOGPS
logP	0.49	ALOGPS
logP	-1.4	ChemAxon
logS	-1.8	ALOGPS
pKa (Strongest Acidic)	2.75	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	211.28 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	78.67 m³·mol⁻¹	ChemAxon
Polarizability	33.42 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	No	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]+	185.068	31661259
DarkChem	[M-H]-	179.929	31661259
DeepCCS	[M+H]+	178.383	30932474
DeepCCS	[M-H]-	176.025	30932474
DeepCCS	[M-2H]-	210.237	30932474
DeepCCS	[M+Na]+	186.06	30932474
AllCCS	[M+H]+	180.5	32859911
AllCCS	[M+H-H2O]+	178.0	32859911
AllCCS	[M+NH4]+	182.8	32859911
AllCCS	[M+Na]+	183.5	32859911
AllCCS	[M-H]-	178.8	32859911
AllCCS	[M+Na-2H]-	178.9	32859911
AllCCS	[M+HCOO]-	179.2	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
6-Methyl 2-galloylgalactarate	COC(=O)C(O)C(O)C(O)C(OC(=O)C1=CC(O)=C(O)C(O)=C1)C(O)=O	5146.4	Standard polar	33892256
6-Methyl 2-galloylgalactarate	COC(=O)C(O)C(O)C(O)C(OC(=O)C1=CC(O)=C(O)C(O)=C1)C(O)=O	2932.3	Standard non polar	33892256
6-Methyl 2-galloylgalactarate	COC(=O)C(O)C(O)C(O)C(OC(=O)C1=CC(O)=C(O)C(O)=C1)C(O)=O	3039.6	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
6-Methyl 2-galloylgalactarate,1TMS,isomer #1	COC(=O)C(O[Si](C)(C)C)C(O)C(O)C(OC(=O)C1=CC(O)=C(O)C(O)=C1)C(=O)O	3198.9	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,1TMS,isomer #2	COC(=O)C(O)C(O[Si](C)(C)C)C(O)C(OC(=O)C1=CC(O)=C(O)C(O)=C1)C(=O)O	3175.6	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,1TMS,isomer #3	COC(=O)C(O)C(O)C(O[Si](C)(C)C)C(OC(=O)C1=CC(O)=C(O)C(O)=C1)C(=O)O	3164.6	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,1TMS,isomer #4	COC(=O)C(O)C(O)C(O)C(OC(=O)C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)C(=O)O	3080.8	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,1TMS,isomer #5	COC(=O)C(O)C(O)C(O)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)C(=O)O	3009.7	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,1TMS,isomer #6	COC(=O)C(O)C(O)C(O)C(OC(=O)C1=CC(O)=C(O)C(O)=C1)C(=O)O[Si](C)(C)C	3139.7	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,2TMS,isomer #1	COC(=O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C(OC(=O)C1=CC(O)=C(O)C(O)=C1)C(=O)O	3148.2	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,2TMS,isomer #10	COC(=O)C(O)C(O)C(O[Si](C)(C)C)C(OC(=O)C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)C(=O)O	3027.3	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,2TMS,isomer #11	COC(=O)C(O)C(O)C(O[Si](C)(C)C)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)C(=O)O	2948.6	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,2TMS,isomer #12	COC(=O)C(O)C(O)C(O[Si](C)(C)C)C(OC(=O)C1=CC(O)=C(O)C(O)=C1)C(=O)O[Si](C)(C)C	3085.4	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,2TMS,isomer #13	COC(=O)C(O)C(O)C(O)C(OC(=O)C1=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C1)C(=O)O	2996.8	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,2TMS,isomer #14	COC(=O)C(O)C(O)C(O)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O	2963.6	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,2TMS,isomer #15	COC(=O)C(O)C(O)C(O)C(OC(=O)C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	2996.0	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,2TMS,isomer #16	COC(=O)C(O)C(O)C(O)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)C(=O)O[Si](C)(C)C	2950.3	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,2TMS,isomer #2	COC(=O)C(O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C(OC(=O)C1=CC(O)=C(O)C(O)=C1)C(=O)O	3143.9	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,2TMS,isomer #3	COC(=O)C(O[Si](C)(C)C)C(O)C(O)C(OC(=O)C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)C(=O)O	3057.3	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,2TMS,isomer #4	COC(=O)C(O[Si](C)(C)C)C(O)C(O)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)C(=O)O	2985.1	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,2TMS,isomer #5	COC(=O)C(O[Si](C)(C)C)C(O)C(O)C(OC(=O)C1=CC(O)=C(O)C(O)=C1)C(=O)O[Si](C)(C)C	3120.1	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,2TMS,isomer #6	COC(=O)C(O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(OC(=O)C1=CC(O)=C(O)C(O)=C1)C(=O)O	3117.4	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,2TMS,isomer #7	COC(=O)C(O)C(O[Si](C)(C)C)C(O)C(OC(=O)C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)C(=O)O	3027.3	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,2TMS,isomer #8	COC(=O)C(O)C(O[Si](C)(C)C)C(O)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)C(=O)O	2968.0	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,2TMS,isomer #9	COC(=O)C(O)C(O[Si](C)(C)C)C(O)C(OC(=O)C1=CC(O)=C(O)C(O)=C1)C(=O)O[Si](C)(C)C	3088.7	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TMS,isomer #1	COC(=O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(OC(=O)C1=CC(O)=C(O)C(O)=C1)C(=O)O	3105.3	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TMS,isomer #10	COC(=O)C(O[Si](C)(C)C)C(O)C(O)C(OC(=O)C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	2938.8	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TMS,isomer #11	COC(=O)C(O[Si](C)(C)C)C(O)C(O)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)C(=O)O[Si](C)(C)C	2935.7	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TMS,isomer #12	COC(=O)C(O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(OC(=O)C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)C(=O)O	2967.6	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TMS,isomer #13	COC(=O)C(O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)C(=O)O	2889.7	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TMS,isomer #14	COC(=O)C(O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(OC(=O)C1=CC(O)=C(O)C(O)=C1)C(=O)O[Si](C)(C)C	3050.5	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TMS,isomer #15	COC(=O)C(O)C(O[Si](C)(C)C)C(O)C(OC(=O)C1=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C1)C(=O)O	2948.4	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TMS,isomer #16	COC(=O)C(O)C(O[Si](C)(C)C)C(O)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O	2921.1	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TMS,isomer #17	COC(=O)C(O)C(O[Si](C)(C)C)C(O)C(OC(=O)C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	2914.7	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TMS,isomer #18	COC(=O)C(O)C(O[Si](C)(C)C)C(O)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)C(=O)O[Si](C)(C)C	2926.4	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TMS,isomer #19	COC(=O)C(O)C(O)C(O[Si](C)(C)C)C(OC(=O)C1=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C1)C(=O)O	2940.8	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TMS,isomer #2	COC(=O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C(OC(=O)C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)C(=O)O	2997.5	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TMS,isomer #20	COC(=O)C(O)C(O)C(O[Si](C)(C)C)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O	2914.1	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TMS,isomer #21	COC(=O)C(O)C(O)C(O[Si](C)(C)C)C(OC(=O)C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	2912.3	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TMS,isomer #22	COC(=O)C(O)C(O)C(O[Si](C)(C)C)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)C(=O)O[Si](C)(C)C	2902.1	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TMS,isomer #23	COC(=O)C(O)C(O)C(O)C(OC(=O)C1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O	2954.6	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TMS,isomer #24	COC(=O)C(O)C(O)C(O)C(OC(=O)C1=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	2914.1	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TMS,isomer #25	COC(=O)C(O)C(O)C(O)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	2891.9	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TMS,isomer #3	COC(=O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)C(=O)O	2912.6	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TMS,isomer #4	COC(=O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C(OC(=O)C1=CC(O)=C(O)C(O)=C1)C(=O)O[Si](C)(C)C	3074.7	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TMS,isomer #5	COC(=O)C(O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C(OC(=O)C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)C(=O)O	2996.2	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TMS,isomer #6	COC(=O)C(O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)C(=O)O	2912.2	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TMS,isomer #7	COC(=O)C(O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C(OC(=O)C1=CC(O)=C(O)C(O)=C1)C(=O)O[Si](C)(C)C	3068.9	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TMS,isomer #8	COC(=O)C(O[Si](C)(C)C)C(O)C(O)C(OC(=O)C1=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C1)C(=O)O	2971.2	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TMS,isomer #9	COC(=O)C(O[Si](C)(C)C)C(O)C(O)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O	2948.3	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TMS,isomer #1	COC(=O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(OC(=O)C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)C(=O)O	2965.3	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TMS,isomer #10	COC(=O)C(O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C(OC(=O)C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	2884.3	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TMS,isomer #11	COC(=O)C(O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)C(=O)O[Si](C)(C)C	2901.2	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TMS,isomer #12	COC(=O)C(O[Si](C)(C)C)C(O)C(O)C(OC(=O)C1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O	2959.1	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TMS,isomer #13	COC(=O)C(O[Si](C)(C)C)C(O)C(O)C(OC(=O)C1=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	2951.8	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TMS,isomer #14	COC(=O)C(O[Si](C)(C)C)C(O)C(O)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	2926.7	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TMS,isomer #15	COC(=O)C(O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(OC(=O)C1=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C1)C(=O)O	2914.7	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TMS,isomer #16	COC(=O)C(O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O	2899.8	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TMS,isomer #17	COC(=O)C(O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(OC(=O)C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	2864.6	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TMS,isomer #18	COC(=O)C(O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)C(=O)O[Si](C)(C)C	2877.3	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TMS,isomer #19	COC(=O)C(O)C(O[Si](C)(C)C)C(O)C(OC(=O)C1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O	2938.1	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TMS,isomer #2	COC(=O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)C(=O)O	2894.6	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TMS,isomer #20	COC(=O)C(O)C(O[Si](C)(C)C)C(O)C(OC(=O)C1=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	2935.3	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TMS,isomer #21	COC(=O)C(O)C(O[Si](C)(C)C)C(O)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	2915.1	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TMS,isomer #22	COC(=O)C(O)C(O)C(O[Si](C)(C)C)C(OC(=O)C1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O	2937.1	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TMS,isomer #23	COC(=O)C(O)C(O)C(O[Si](C)(C)C)C(OC(=O)C1=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	2906.7	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TMS,isomer #24	COC(=O)C(O)C(O)C(O[Si](C)(C)C)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	2886.5	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TMS,isomer #25	COC(=O)C(O)C(O)C(O)C(OC(=O)C1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	2909.3	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TMS,isomer #3	COC(=O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(OC(=O)C1=CC(O)=C(O)C(O)=C1)C(=O)O[Si](C)(C)C	3031.6	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TMS,isomer #4	COC(=O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C(OC(=O)C1=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C1)C(=O)O	2924.5	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TMS,isomer #5	COC(=O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O	2915.6	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TMS,isomer #6	COC(=O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C(OC(=O)C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	2883.9	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TMS,isomer #7	COC(=O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)C(=O)O[Si](C)(C)C	2894.1	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TMS,isomer #8	COC(=O)C(O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C(OC(=O)C1=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C1)C(=O)O	2929.8	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TMS,isomer #9	COC(=O)C(O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O	2915.9	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,5TMS,isomer #1	COC(=O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(OC(=O)C1=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C1)C(=O)O	2922.4	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,5TMS,isomer #10	COC(=O)C(O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	2919.9	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,5TMS,isomer #11	COC(=O)C(O[Si](C)(C)C)C(O)C(O)C(OC(=O)C1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	2943.4	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,5TMS,isomer #12	COC(=O)C(O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(OC(=O)C1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O	2934.4	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,5TMS,isomer #13	COC(=O)C(O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(OC(=O)C1=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	2889.9	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,5TMS,isomer #14	COC(=O)C(O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	2889.4	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,5TMS,isomer #15	COC(=O)C(O)C(O[Si](C)(C)C)C(O)C(OC(=O)C1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	2937.5	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,5TMS,isomer #16	COC(=O)C(O)C(O)C(O[Si](C)(C)C)C(OC(=O)C1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	2909.0	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,5TMS,isomer #2	COC(=O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O	2911.6	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,5TMS,isomer #3	COC(=O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(OC(=O)C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	2863.4	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,5TMS,isomer #4	COC(=O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)C(=O)O[Si](C)(C)C	2878.3	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,5TMS,isomer #5	COC(=O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C(OC(=O)C1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O	2941.1	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,5TMS,isomer #6	COC(=O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C(OC(=O)C1=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	2914.0	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,5TMS,isomer #7	COC(=O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	2912.4	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,5TMS,isomer #8	COC(=O)C(O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C(OC(=O)C1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O	2946.5	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,5TMS,isomer #9	COC(=O)C(O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C(OC(=O)C1=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	2918.7	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,6TMS,isomer #1	COC(=O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(OC(=O)C1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O	2943.1	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,6TMS,isomer #2	COC(=O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(OC(=O)C1=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	2903.1	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,6TMS,isomer #3	COC(=O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	2911.1	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,6TMS,isomer #4	COC(=O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C(OC(=O)C1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	2938.9	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,6TMS,isomer #5	COC(=O)C(O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C(OC(=O)C1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	2942.9	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,6TMS,isomer #6	COC(=O)C(O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(OC(=O)C1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	2916.6	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,7TMS,isomer #1	COC(=O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(OC(=O)C1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	2940.0	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,1TBDMS,isomer #1	COC(=O)C(O[Si](C)(C)C(C)(C)C)C(O)C(O)C(OC(=O)C1=CC(O)=C(O)C(O)=C1)C(=O)O	3428.6	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,1TBDMS,isomer #2	COC(=O)C(O)C(O[Si](C)(C)C(C)(C)C)C(O)C(OC(=O)C1=CC(O)=C(O)C(O)=C1)C(=O)O	3402.4	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,1TBDMS,isomer #3	COC(=O)C(O)C(O)C(O[Si](C)(C)C(C)(C)C)C(OC(=O)C1=CC(O)=C(O)C(O)=C1)C(=O)O	3400.1	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,1TBDMS,isomer #4	COC(=O)C(O)C(O)C(O)C(OC(=O)C1=CC(O)=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O	3309.0	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,1TBDMS,isomer #5	COC(=O)C(O)C(O)C(O)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)C(=O)O	3278.4	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,1TBDMS,isomer #6	COC(=O)C(O)C(O)C(O)C(OC(=O)C1=CC(O)=C(O)C(O)=C1)C(=O)O[Si](C)(C)C(C)(C)C	3392.2	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,2TBDMS,isomer #1	COC(=O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C(OC(=O)C1=CC(O)=C(O)C(O)=C1)C(=O)O	3532.7	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,2TBDMS,isomer #10	COC(=O)C(O)C(O)C(O[Si](C)(C)C(C)(C)C)C(OC(=O)C1=CC(O)=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O	3428.0	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,2TBDMS,isomer #11	COC(=O)C(O)C(O)C(O[Si](C)(C)C(C)(C)C)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)C(=O)O	3424.2	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,2TBDMS,isomer #12	COC(=O)C(O)C(O)C(O[Si](C)(C)C(C)(C)C)C(OC(=O)C1=CC(O)=C(O)C(O)=C1)C(=O)O[Si](C)(C)C(C)(C)C	3509.8	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,2TBDMS,isomer #13	COC(=O)C(O)C(O)C(O)C(OC(=O)C1=CC(O[Si](C)(C)C(C)(C)C)=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O	3421.6	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,2TBDMS,isomer #14	COC(=O)C(O)C(O)C(O)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O	3412.8	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,2TBDMS,isomer #15	COC(=O)C(O)C(O)C(O)C(OC(=O)C1=CC(O)=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O[Si](C)(C)C(C)(C)C	3440.4	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,2TBDMS,isomer #16	COC(=O)C(O)C(O)C(O)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)C(=O)O[Si](C)(C)C(C)(C)C	3463.1	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,2TBDMS,isomer #2	COC(=O)C(O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C(OC(=O)C1=CC(O)=C(O)C(O)=C1)C(=O)O	3532.3	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,2TBDMS,isomer #3	COC(=O)C(O[Si](C)(C)C(C)(C)C)C(O)C(O)C(OC(=O)C1=CC(O)=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O	3457.5	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,2TBDMS,isomer #4	COC(=O)C(O[Si](C)(C)C(C)(C)C)C(O)C(O)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)C(=O)O	3461.6	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,2TBDMS,isomer #5	COC(=O)C(O[Si](C)(C)C(C)(C)C)C(O)C(O)C(OC(=O)C1=CC(O)=C(O)C(O)=C1)C(=O)O[Si](C)(C)C(C)(C)C	3543.1	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,2TBDMS,isomer #6	COC(=O)C(O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(OC(=O)C1=CC(O)=C(O)C(O)=C1)C(=O)O	3500.7	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,2TBDMS,isomer #7	COC(=O)C(O)C(O[Si](C)(C)C(C)(C)C)C(O)C(OC(=O)C1=CC(O)=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O	3423.7	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,2TBDMS,isomer #8	COC(=O)C(O)C(O[Si](C)(C)C(C)(C)C)C(O)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)C(=O)O	3440.4	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,2TBDMS,isomer #9	COC(=O)C(O)C(O[Si](C)(C)C(C)(C)C)C(O)C(OC(=O)C1=CC(O)=C(O)C(O)=C1)C(=O)O[Si](C)(C)C(C)(C)C	3513.1	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TBDMS,isomer #1	COC(=O)C(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)C(OC(=O)C1=CC(O)=C(O)C(O)=C1)C(=O)O	3643.0	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TBDMS,isomer #10	COC(=O)C(O[Si](C)(C)C(C)(C)C)C(O)C(O)C(OC(=O)C1=CC(O)=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O[Si](C)(C)C(C)(C)C	3596.7	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TBDMS,isomer #11	COC(=O)C(O[Si](C)(C)C(C)(C)C)C(O)C(O)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)C(=O)O[Si](C)(C)C(C)(C)C	3682.6	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TBDMS,isomer #12	COC(=O)C(O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(OC(=O)C1=CC(O)=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O	3563.2	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TBDMS,isomer #13	COC(=O)C(O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)C(=O)O	3598.2	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TBDMS,isomer #14	COC(=O)C(O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(OC(=O)C1=CC(O)=C(O)C(O)=C1)C(=O)O[Si](C)(C)C(C)(C)C	3622.3	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TBDMS,isomer #15	COC(=O)C(O)C(O[Si](C)(C)C(C)(C)C)C(O)C(OC(=O)C1=CC(O[Si](C)(C)C(C)(C)C)=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O	3614.0	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TBDMS,isomer #16	COC(=O)C(O)C(O[Si](C)(C)C(C)(C)C)C(O)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O	3593.9	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TBDMS,isomer #17	COC(=O)C(O)C(O[Si](C)(C)C(C)(C)C)C(O)C(OC(=O)C1=CC(O)=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O[Si](C)(C)C(C)(C)C	3577.9	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TBDMS,isomer #18	COC(=O)C(O)C(O[Si](C)(C)C(C)(C)C)C(O)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)C(=O)O[Si](C)(C)C(C)(C)C	3659.0	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TBDMS,isomer #19	COC(=O)C(O)C(O)C(O[Si](C)(C)C(C)(C)C)C(OC(=O)C1=CC(O[Si](C)(C)C(C)(C)C)=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O	3584.6	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TBDMS,isomer #2	COC(=O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C(OC(=O)C1=CC(O)=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O	3583.2	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TBDMS,isomer #20	COC(=O)C(O)C(O)C(O[Si](C)(C)C(C)(C)C)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O	3570.5	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TBDMS,isomer #21	COC(=O)C(O)C(O)C(O[Si](C)(C)C(C)(C)C)C(OC(=O)C1=CC(O)=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O[Si](C)(C)C(C)(C)C	3571.5	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TBDMS,isomer #22	COC(=O)C(O)C(O)C(O[Si](C)(C)C(C)(C)C)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)C(=O)O[Si](C)(C)C(C)(C)C	3636.8	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TBDMS,isomer #23	COC(=O)C(O)C(O)C(O)C(OC(=O)C1=CC(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)=C1)C(=O)O	3574.3	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TBDMS,isomer #24	COC(=O)C(O)C(O)C(O)C(OC(=O)C1=CC(O[Si](C)(C)C(C)(C)C)=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O[Si](C)(C)C(C)(C)C	3622.5	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TBDMS,isomer #25	COC(=O)C(O)C(O)C(O)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O[Si](C)(C)C(C)(C)C	3600.4	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TBDMS,isomer #3	COC(=O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)C(=O)O	3631.9	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TBDMS,isomer #4	COC(=O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C(OC(=O)C1=CC(O)=C(O)C(O)=C1)C(=O)O[Si](C)(C)C(C)(C)C	3645.4	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TBDMS,isomer #5	COC(=O)C(O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C(OC(=O)C1=CC(O)=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O	3584.4	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TBDMS,isomer #6	COC(=O)C(O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)C(=O)O	3627.4	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TBDMS,isomer #7	COC(=O)C(O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C(OC(=O)C1=CC(O)=C(O)C(O)=C1)C(=O)O[Si](C)(C)C(C)(C)C	3654.7	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TBDMS,isomer #8	COC(=O)C(O[Si](C)(C)C(C)(C)C)C(O)C(O)C(OC(=O)C1=CC(O[Si](C)(C)C(C)(C)C)=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O	3638.4	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,3TBDMS,isomer #9	COC(=O)C(O[Si](C)(C)C(C)(C)C)C(O)C(O)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O	3616.8	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TBDMS,isomer #1	COC(=O)C(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)C(OC(=O)C1=CC(O)=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O	3724.4	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TBDMS,isomer #10	COC(=O)C(O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C(OC(=O)C1=CC(O)=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O[Si](C)(C)C(C)(C)C	3754.8	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TBDMS,isomer #11	COC(=O)C(O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)C(=O)O[Si](C)(C)C(C)(C)C	3848.4	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TBDMS,isomer #12	COC(=O)C(O[Si](C)(C)C(C)(C)C)C(O)C(O)C(OC(=O)C1=CC(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)=C1)C(=O)O	3798.4	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TBDMS,isomer #13	COC(=O)C(O[Si](C)(C)C(C)(C)C)C(O)C(O)C(OC(=O)C1=CC(O[Si](C)(C)C(C)(C)C)=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O[Si](C)(C)C(C)(C)C	3859.8	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TBDMS,isomer #14	COC(=O)C(O[Si](C)(C)C(C)(C)C)C(O)C(O)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O[Si](C)(C)C(C)(C)C	3830.3	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TBDMS,isomer #15	COC(=O)C(O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(OC(=O)C1=CC(O[Si](C)(C)C(C)(C)C)=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O	3784.3	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TBDMS,isomer #16	COC(=O)C(O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O	3755.4	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TBDMS,isomer #17	COC(=O)C(O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(OC(=O)C1=CC(O)=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O[Si](C)(C)C(C)(C)C	3721.2	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TBDMS,isomer #18	COC(=O)C(O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)C(=O)O[Si](C)(C)C(C)(C)C	3812.7	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TBDMS,isomer #19	COC(=O)C(O)C(O[Si](C)(C)C(C)(C)C)C(O)C(OC(=O)C1=CC(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)=C1)C(=O)O	3778.9	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TBDMS,isomer #2	COC(=O)C(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)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)C(=O)O	3790.1	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TBDMS,isomer #20	COC(=O)C(O)C(O[Si](C)(C)C(C)(C)C)C(O)C(OC(=O)C1=CC(O[Si](C)(C)C(C)(C)C)=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O[Si](C)(C)C(C)(C)C	3844.6	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TBDMS,isomer #21	COC(=O)C(O)C(O[Si](C)(C)C(C)(C)C)C(O)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O[Si](C)(C)C(C)(C)C	3813.7	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TBDMS,isomer #22	COC(=O)C(O)C(O)C(O[Si](C)(C)C(C)(C)C)C(OC(=O)C1=CC(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)=C1)C(=O)O	3756.7	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TBDMS,isomer #23	COC(=O)C(O)C(O)C(O[Si](C)(C)C(C)(C)C)C(OC(=O)C1=CC(O[Si](C)(C)C(C)(C)C)=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O[Si](C)(C)C(C)(C)C	3815.1	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TBDMS,isomer #24	COC(=O)C(O)C(O)C(O[Si](C)(C)C(C)(C)C)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O[Si](C)(C)C(C)(C)C	3780.4	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TBDMS,isomer #25	COC(=O)C(O)C(O)C(O)C(OC(=O)C1=CC(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)=C1)C(=O)O[Si](C)(C)C(C)(C)C	3782.5	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TBDMS,isomer #3	COC(=O)C(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)C(OC(=O)C1=CC(O)=C(O)C(O)=C1)C(=O)O[Si](C)(C)C(C)(C)C	3760.7	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TBDMS,isomer #4	COC(=O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C(OC(=O)C1=CC(O[Si](C)(C)C(C)(C)C)=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O	3803.1	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TBDMS,isomer #5	COC(=O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O	3773.2	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TBDMS,isomer #6	COC(=O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C(OC(=O)C1=CC(O)=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O[Si](C)(C)C(C)(C)C	3742.5	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TBDMS,isomer #7	COC(=O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)C(=O)O[Si](C)(C)C(C)(C)C	3833.0	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TBDMS,isomer #8	COC(=O)C(O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C(OC(=O)C1=CC(O[Si](C)(C)C(C)(C)C)=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O	3804.2	Semi standard non polar	33892256
6-Methyl 2-galloylgalactarate,4TBDMS,isomer #9	COC(=O)C(O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C(OC(=O)C1=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O	3771.9	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 - 6-Methyl 2-galloylgalactarate GC-MS (Non-derivatized) - 70eV, Positive	splash10-0zfr-6912000000-8cd753abaf2d0b8d0f73	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-Methyl 2-galloylgalactarate GC-MS (4 TMS) - 70eV, Positive	splash10-004i-4091001000-7d315c5a65ba7048ad0a	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-Methyl 2-galloylgalactarate 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-Methyl 2-galloylgalactarate 10V, Positive-QTOF	splash10-0pdi-1749000000-f68c4f1c8d6db3243d2e	2016-08-02	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Methyl 2-galloylgalactarate 20V, Positive-QTOF	splash10-102i-4951000000-a0997f0761a8bc2f6cd7	2016-08-02	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Methyl 2-galloylgalactarate 40V, Positive-QTOF	splash10-0udi-5900000000-0a24712763f5d20569da	2016-08-02	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Methyl 2-galloylgalactarate 10V, Negative-QTOF	splash10-0170-6792000000-d3247f0480b0e1e3b56c	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Methyl 2-galloylgalactarate 20V, Negative-QTOF	splash10-0670-6940000000-e50d2e5586ba43d019a6	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Methyl 2-galloylgalactarate 40V, Negative-QTOF	splash10-016r-3920000000-62bec7203baca04558a3	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Methyl 2-galloylgalactarate 10V, Negative-QTOF	splash10-0550-8594000000-dd541c51ffdc0e721406	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Methyl 2-galloylgalactarate 20V, Negative-QTOF	splash10-00kr-8890000000-4080917be638754f0a7c	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Methyl 2-galloylgalactarate 40V, Negative-QTOF	splash10-004i-3900000000-a83843300bf39a271c3e	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Methyl 2-galloylgalactarate 10V, Positive-QTOF	splash10-0zfr-2669000000-07e64dc73435898f3a19	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Methyl 2-galloylgalactarate 20V, Positive-QTOF	splash10-0nmr-8980000000-94dc34212f6058161e87	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Methyl 2-galloylgalactarate 40V, Positive-QTOF	splash10-0udi-4910000000-2eeabc44219168bf5124	2021-09-25	Wishart Lab	View Spectrum

NMR Spectra

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

Biological Properties

Cellular Locations

Cytoplasm
Extracellular

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB015903

KNApSAcK ID

Not Available

Chemspider ID

35014324

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

75060827

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

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

Showing metabocard for 6-Methyl 2-galloylgalactarate (HMDB0036934)

MOL for HMDB0036934 (6-Methyl 2-galloylgalactarate)

3D MOL for HMDB0036934 (6-Methyl 2-galloylgalactarate)

3D SDF for HMDB0036934 (6-Methyl 2-galloylgalactarate)

3D-SDF for HMDB0036934 (6-Methyl 2-galloylgalactarate)

PDB for HMDB0036934 (6-Methyl 2-galloylgalactarate)

3D PDB for HMDB0036934 (6-Methyl 2-galloylgalactarate)

SMILES for HMDB0036934 (6-Methyl 2-galloylgalactarate)

INCHI for HMDB0036934 (6-Methyl 2-galloylgalactarate)

Structure for HMDB0036934 (6-Methyl 2-galloylgalactarate)

3D Structure for HMDB0036934 (6-Methyl 2-galloylgalactarate)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra