Jump To Section:

Identification Taxonomy Ontology Physical properties Spectra Biological properties Concentrations Links References enzymes (1) Show 1 protein XML

Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-10-30 10:32:48 UTC

Update Date

2022-03-07 03:17:34 UTC

HMDB ID

HMDB0059651

Secondary Accession Numbers

HMDB59651

Metabolite Identification

Common Name

2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate

Description

2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate, also known as 2-protocatechuoyl phloroglucinolcarboxylate or 2,4Dioh-6(2,4Diohbenacid)benzacid, belongs to the class of organic compounds known as depsides and depsidones. These are polycyclic compounds that is either a polyphenolic compound composed of two or more monocyclic aromatic units linked by an ester bond (depside), or a compound containing the depsidone structure (depsidone). 2-(3,4-dihydroxybenzoyloxy)-4,6-dihydroxybenzoate is part of the Flavonoid metabolism pathway. 2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate is an extremely weak basic (essentially neutral) compound (based on its pKa). 2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate exists in all living organisms, ranging from bacteria to humans.

Structure

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

HMDB0059651
     RDKit          3D
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate
 32 33  0  0  0  0  0  0  0  0999 V2000
   -0.1205   -0.9930    1.5059 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5296   -0.2230    0.6069 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3834    0.5509   -0.0485 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7227    0.5908    0.1599 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2444    1.4430    1.1056 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6174    1.4698    1.3048 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1350    2.3453    2.2741 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4809    0.6816    0.5982 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9197   -0.1839   -0.3662 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8023   -0.9661   -1.0642 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5601   -0.2364   -0.5904 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9158   -1.0896   -1.5552 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6738   -1.0881   -1.7090 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6282   -1.9475   -2.3553 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9363   -0.1358    0.2501 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3441    0.7247   -0.7453 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6746    0.8313   -1.1085 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6489    0.0911   -0.5006 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9729    0.2004   -0.8655 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2474   -0.7831    0.5082 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2545   -1.5221    1.1086 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9185   -0.8887    0.8700 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5946    2.0914    1.6944 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5507    2.9486    2.8245 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5526    0.6926    0.7436 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6790   -1.6239   -1.7592 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5866   -2.9489   -2.3411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6256    1.3467   -1.2748 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9401    1.5227   -1.8966 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2191    0.8460   -1.6010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9773   -2.1632    1.8452 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6378   -1.5835    1.6646 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  1  0
  6  8  2  0
  8  9  1  0
  9 10  1  0
  9 11  2  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
  2 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20 22  2  0
 11  4  1  0
 22 15  1  0
  5 23  1  0
  7 24  1  0
  8 25  1  0
 10 26  1  0
 14 27  1  0
 16 28  1  0
 17 29  1  0
 19 30  1  0
 21 31  1  0
 22 32  1  0
M  END


  Mrv0541 10101211222D          

 22 23  0  0  0  0            999 V2000
    5.0013    1.2375    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
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    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
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    2.4750    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   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    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
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    0.0000 C   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
    4.2868    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    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
    1.4289   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  2  0  0  0  0
  6  1  1  0  0  0  0
  6  3  2  0  0  0  0
  7  4  2  0  0  0  0
  7  5  1  0  0  0  0
  8  2  1  0  0  0  0
  9  3  1  0  0  0  0
  9  8  2  0  0  0  0
 10  4  1  0  0  0  0
 11  5  2  0  0  0  0
 12 10  2  0  0  0  0
 12 11  1  0  0  0  0
 13 12  1  0  0  0  0
 14  6  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 10  1  0  0  0  0
 19 13  2  0  0  0  0
 20 13  1  0  0  0  0
 21 14  2  0  0  0  0
 22 11  1  0  0  0  0
 22 14  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0059651

> <DATABASE_NAME>
hmdb

> <SMILES>
OC(=O)C1=C(O)C=C(O)C=C1OC(=O)C1=CC(O)=C(O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C14H10O8/c15-7-4-10(18)12(13(19)20)11(5-7)22-14(21)6-1-2-8(16)9(17)3-6/h1-5,15-18H,(H,19,20)

> <INCHI_KEY>
GRXIELRCPYIEQI-UHFFFAOYSA-N

> <FORMULA>
C14H10O8

> <MOLECULAR_WEIGHT>
306.2244

> <EXACT_MASS>
306.037567296

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_AVERAGE_POLARIZABILITY>
27.888505590538912

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-(3,4-dihydroxybenzoyloxy)-4,6-dihydroxybenzoic acid

> <ALOGPS_LOGP>
2.47

> <JCHEM_LOGP>
2.7280028499999998

> <ALOGPS_LOGS>
-3.12

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.46858192613729

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.446274683898726

> <JCHEM_PKA_STRONGEST_BASIC>
-5.821978101135998

> <JCHEM_POLAR_SURFACE_AREA>
144.52

> <JCHEM_REFRACTIVITY>
73.0407

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.31e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-(3,4-dihydroxybenzoyloxy)-4,6-dihydroxybenzoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0059651
     RDKit          3D
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate
 32 33  0  0  0  0  0  0  0  0999 V2000
   -0.1205   -0.9930    1.5059 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5296   -0.2230    0.6069 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3834    0.5509   -0.0485 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7227    0.5908    0.1599 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2444    1.4430    1.1056 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6174    1.4698    1.3048 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1350    2.3453    2.2741 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4809    0.6816    0.5982 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9197   -0.1839   -0.3662 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8023   -0.9661   -1.0642 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5601   -0.2364   -0.5904 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9158   -1.0896   -1.5552 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6738   -1.0881   -1.7090 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6282   -1.9475   -2.3553 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9363   -0.1358    0.2501 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3441    0.7247   -0.7453 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6746    0.8313   -1.1085 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6489    0.0911   -0.5006 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9729    0.2004   -0.8655 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2474   -0.7831    0.5082 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2545   -1.5221    1.1086 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9185   -0.8887    0.8700 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5946    2.0914    1.6944 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5507    2.9486    2.8245 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5526    0.6926    0.7436 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6790   -1.6239   -1.7592 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5866   -2.9489   -2.3411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6256    1.3467   -1.2748 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9401    1.5227   -1.8966 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2191    0.8460   -1.6010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9773   -2.1632    1.8452 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6378   -1.5835    1.6646 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  1  0
  6  8  2  0
  8  9  1  0
  9 10  1  0
  9 11  2  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
  2 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20 22  2  0
 11  4  1  0
 22 15  1  0
  5 23  1  0
  7 24  1  0
  8 25  1  0
 10 26  1  0
 14 27  1  0
 16 28  1  0
 17 29  1  0
 19 30  1  0
 21 31  1  0
 22 32  1  0
M  END

HEADER    PROTEIN                                 10-OCT-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-OCT-12         0                                  
HETATM    1  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    8                                                       
CONECT    3    6    9                                                       
CONECT    4    7   10                                                       
CONECT    5    7   11                                                       
CONECT    6    1    3   14                                                  
CONECT    7    4    5   15                                                  
CONECT    8    2    9   16                                                  
CONECT    9    3    8   17                                                  
CONECT   10    4   12   18                                                  
CONECT   11    5   12   22                                                  
CONECT   12   10   11   13                                                  
CONECT   13   12   19   20                                                  
CONECT   14    6   21   22                                                  
CONECT   15    7                                                            
CONECT   16    8                                                            
CONECT   17    9                                                            
CONECT   18   10                                                            
CONECT   19   13                                                            
CONECT   20   13                                                            
CONECT   21   14                                                            
CONECT   22   11   14                                                       
MASTER        0    0    0    0    0    0    0    0   22    0   46    0
END

COMPND    HMDB0059651
HETATM    1  O1  UNL     1      -0.121  -0.993   1.506  1.00  0.00           O  
HETATM    2  C1  UNL     1      -0.530  -0.223   0.607  1.00  0.00           C  
HETATM    3  O2  UNL     1       0.383   0.551  -0.049  1.00  0.00           O  
HETATM    4  C2  UNL     1       1.723   0.591   0.160  1.00  0.00           C  
HETATM    5  C3  UNL     1       2.244   1.443   1.106  1.00  0.00           C  
HETATM    6  C4  UNL     1       3.617   1.470   1.305  1.00  0.00           C  
HETATM    7  O3  UNL     1       4.135   2.345   2.274  1.00  0.00           O  
HETATM    8  C5  UNL     1       4.481   0.682   0.598  1.00  0.00           C  
HETATM    9  C6  UNL     1       3.920  -0.184  -0.366  1.00  0.00           C  
HETATM   10  O4  UNL     1       4.802  -0.966  -1.064  1.00  0.00           O  
HETATM   11  C7  UNL     1       2.560  -0.236  -0.590  1.00  0.00           C  
HETATM   12  C8  UNL     1       1.916  -1.090  -1.555  1.00  0.00           C  
HETATM   13  O5  UNL     1       0.674  -1.088  -1.709  1.00  0.00           O  
HETATM   14  O6  UNL     1       2.628  -1.947  -2.355  1.00  0.00           O  
HETATM   15  C9  UNL     1      -1.936  -0.136   0.250  1.00  0.00           C  
HETATM   16  C10 UNL     1      -2.344   0.725  -0.745  1.00  0.00           C  
HETATM   17  C11 UNL     1      -3.675   0.831  -1.108  1.00  0.00           C  
HETATM   18  C12 UNL     1      -4.649   0.091  -0.501  1.00  0.00           C  
HETATM   19  O7  UNL     1      -5.973   0.200  -0.865  1.00  0.00           O  
HETATM   20  C13 UNL     1      -4.247  -0.783   0.508  1.00  0.00           C  
HETATM   21  O8  UNL     1      -5.254  -1.522   1.109  1.00  0.00           O  
HETATM   22  C14 UNL     1      -2.919  -0.889   0.870  1.00  0.00           C  
HETATM   23  H1  UNL     1       1.595   2.091   1.694  1.00  0.00           H  
HETATM   24  H2  UNL     1       3.551   2.949   2.825  1.00  0.00           H  
HETATM   25  H3  UNL     1       5.553   0.693   0.744  1.00  0.00           H  
HETATM   26  H4  UNL     1       4.679  -1.624  -1.759  1.00  0.00           H  
HETATM   27  H5  UNL     1       2.587  -2.949  -2.341  1.00  0.00           H  
HETATM   28  H6  UNL     1      -1.626   1.347  -1.275  1.00  0.00           H  
HETATM   29  H7  UNL     1      -3.940   1.523  -1.897  1.00  0.00           H  
HETATM   30  H8  UNL     1      -6.219   0.846  -1.601  1.00  0.00           H  
HETATM   31  H9  UNL     1      -4.977  -2.163   1.845  1.00  0.00           H  
HETATM   32  H10 UNL     1      -2.638  -1.583   1.665  1.00  0.00           H  
CONECT    1    2    2
CONECT    2    3   15
CONECT    3    4
CONECT    4    5    5   11
CONECT    5    6   23
CONECT    6    7    8    8
CONECT    7   24
CONECT    8    9   25
CONECT    9   10   11   11
CONECT   10   26
CONECT   11   12
CONECT   12   13   13   14
CONECT   14   27
CONECT   15   16   16   22
CONECT   16   17   28
CONECT   17   18   18   29
CONECT   18   19   20
CONECT   19   30
CONECT   20   21   22   22
CONECT   21   31
CONECT   22   32
END

HMDB0059651
     RDKit          3D
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate
 32 33  0  0  0  0  0  0  0  0999 V2000
   -0.1205   -0.9930    1.5059 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5296   -0.2230    0.6069 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3834    0.5509   -0.0485 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7227    0.5908    0.1599 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2444    1.4430    1.1056 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6174    1.4698    1.3048 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1350    2.3453    2.2741 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4809    0.6816    0.5982 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9197   -0.1839   -0.3662 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8023   -0.9661   -1.0642 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5601   -0.2364   -0.5904 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9158   -1.0896   -1.5552 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6738   -1.0881   -1.7090 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6282   -1.9475   -2.3553 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9363   -0.1358    0.2501 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3441    0.7247   -0.7453 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6746    0.8313   -1.1085 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6489    0.0911   -0.5006 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9729    0.2004   -0.8655 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2474   -0.7831    0.5082 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2545   -1.5221    1.1086 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9185   -0.8887    0.8700 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5946    2.0914    1.6944 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5507    2.9486    2.8245 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5526    0.6926    0.7436 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6790   -1.6239   -1.7592 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5866   -2.9489   -2.3411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6256    1.3467   -1.2748 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9401    1.5227   -1.8966 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2191    0.8460   -1.6010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9773   -2.1632    1.8452 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6378   -1.5835    1.6646 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  1  0
  6  8  2  0
  8  9  1  0
  9 10  1  0
  9 11  2  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
  2 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20 22  2  0
 11  4  1  0
 22 15  1  0
  5 23  1  0
  7 24  1  0
  8 25  1  0
 10 26  1  0
 14 27  1  0
 16 28  1  0
 17 29  1  0
 19 30  1  0
 21 31  1  0
 22 32  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
2,4DIOH-6(2,4Diohbenacid)benzacid	ChEBI
2-Protocatechuoyl phloroglucinolcarboxylate	ChEBI
2PCPGCA	ChEBI
2-Protocatechuoyl phloroglucinolcarboxylic acid	Generator
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoic acid	Generator
2-Protocatechoylphloroglucinolcarboxylate	HMDB
2-Protocatechoylphloroglucinolcarboxylic acid	HMDB
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate	ChEBI

Chemical Formula

C₁₄H₁₀O₈

Average Molecular Weight

306.2244

Monoisotopic Molecular Weight

306.037567296

IUPAC Name

2-(3,4-dihydroxybenzoyloxy)-4,6-dihydroxybenzoic acid

Traditional Name

2-(3,4-dihydroxybenzoyloxy)-4,6-dihydroxybenzoic acid

CAS Registry Number

Not Available

SMILES

OC(=O)C1=C(O)C=C(O)C=C1OC(=O)C1=CC(O)=C(O)C=C1

InChI Identifier

InChI=1S/C14H10O8/c15-7-4-10(18)12(13(19)20)11(5-7)22-14(21)6-1-2-8(16)9(17)3-6/h1-5,15-18H,(H,19,20)

InChI Key

GRXIELRCPYIEQI-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as depsides and depsidones. These are polycyclic compounds that is either a polyphenolic compound composed of two or more monocyclic aromatic units linked by an ester bond (depside), or a compound containing the depsidone structure (depsidone).

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Depsides and depsidones

Sub Class

Not Available

Direct Parent

Depsides and depsidones

Alternative Parents

Substituents

Depside backbone
M-hydroxybenzoic acid ester
P-hydroxybenzoic acid ester
Dihydroxybenzoic acid
Hydroxybenzoic acid
Phenol ester
Salicylic acid or derivatives
Salicylic acid
Benzoate ester
Benzoic acid
Benzoic acid or derivatives
Phenoxy compound
Resorcinol
Catechol
Benzoyl
Phenol
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Benzenoid
Dicarboxylic acid or derivatives
Monocyclic benzene moiety
Vinylogous acid
Carboxylic acid ester
Carboxylic acid derivative
Carboxylic acid
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

benzoate ester (CHEBI:16068 )
dihydroxybenzoic acid (CHEBI:16068 )

Ontology

Not Available

Physical Properties

State

Solid

Experimental Molecular Properties

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

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.23 g/L	ALOGPS
logP	2.47	ALOGPS
logP	2.73	ChemAxon
logS	-3.1	ALOGPS
pKa (Strongest Acidic)	2.45	ChemAxon
pKa (Strongest Basic)	-5.8	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	144.52 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	73.04 m³·mol⁻¹	ChemAxon
Polarizability	27.89 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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]+	170.257	31661259
DarkChem	[M-H]-	167.006	31661259
DeepCCS	[M+H]+	170.738	30932474
DeepCCS	[M-H]-	168.38	30932474
DeepCCS	[M-2H]-	202.175	30932474
DeepCCS	[M+Na]+	177.403	30932474
AllCCS	[M+H]+	167.2	32859911
AllCCS	[M+H-H2O]+	163.8	32859911
AllCCS	[M+NH4]+	170.3	32859911
AllCCS	[M+Na]+	171.2	32859911
AllCCS	[M-H]-	164.5	32859911
AllCCS	[M+Na-2H]-	164.0	32859911
AllCCS	[M+HCOO]-	163.5	32859911

Predicted Retention Times

Underivatized

Chromatographic Method	Retention Time	Reference
Measured using a Waters Acquity ultraperformance liquid chromatography (UPLC) ethylene-bridged hybrid (BEH) C18 column (100 mm √ó 2.1 mm; 1.7 Œºmparticle diameter). Predicted by Afia on May 17, 2022.	5.3 minutes	32390414
Predicted by Siyang on May 30, 2022	11.0246 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	3.83 minutes	32390414
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	1313.8 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	230.2 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	79.7 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	143.4 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	92.6 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	486.3 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	395.3 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	217.3 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	691.7 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	322.1 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	1248.5 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	244.3 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	302.9 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	570.5 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	188.9 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	402.8 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate	OC(=O)C1=C(O)C=C(O)C=C1OC(=O)C1=CC(O)=C(O)C=C1	4489.8	Standard polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate	OC(=O)C1=C(O)C=C(O)C=C1OC(=O)C1=CC(O)=C(O)C=C1	2852.6	Standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate	OC(=O)C1=C(O)C=C(O)C=C1OC(=O)C1=CC(O)=C(O)C=C1	2871.1	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,1TMS,isomer #1	C[Si](C)(C)OC(=O)C1=C(O)C=C(O)C=C1OC(=O)C1=CC=C(O)C(O)=C1	3077.4	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,1TMS,isomer #2	C[Si](C)(C)OC1=CC(O)=CC(OC(=O)C2=CC=C(O)C(O)=C2)=C1C(=O)O	2966.4	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,1TMS,isomer #3	C[Si](C)(C)OC1=CC(O)=C(C(=O)O)C(OC(=O)C2=CC=C(O)C(O)=C2)=C1	2959.1	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,1TMS,isomer #4	C[Si](C)(C)OC1=CC(C(=O)OC2=CC(O)=CC(O)=C2C(=O)O)=CC=C1O	2930.7	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,1TMS,isomer #5	C[Si](C)(C)OC1=CC=C(C(=O)OC2=CC(O)=CC(O)=C2C(=O)O)C=C1O	2963.8	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,2TMS,isomer #1	C[Si](C)(C)OC(=O)C1=C(OC(=O)C2=CC=C(O)C(O)=C2)C=C(O)C=C1O[Si](C)(C)C	2991.4	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,2TMS,isomer #10	C[Si](C)(C)OC1=CC=C(C(=O)OC2=CC(O)=CC(O)=C2C(=O)O)C=C1O[Si](C)(C)C	2859.8	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,2TMS,isomer #2	C[Si](C)(C)OC(=O)C1=C(O)C=C(O[Si](C)(C)C)C=C1OC(=O)C1=CC=C(O)C(O)=C1	2954.7	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,2TMS,isomer #3	C[Si](C)(C)OC(=O)C1=C(O)C=C(O)C=C1OC(=O)C1=CC=C(O[Si](C)(C)C)C(O)=C1	2928.2	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,2TMS,isomer #4	C[Si](C)(C)OC(=O)C1=C(O)C=C(O)C=C1OC(=O)C1=CC=C(O)C(O[Si](C)(C)C)=C1	2926.4	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,2TMS,isomer #5	C[Si](C)(C)OC1=CC(OC(=O)C2=CC=C(O)C(O)=C2)=C(C(=O)O)C(O[Si](C)(C)C)=C1	2890.8	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,2TMS,isomer #6	C[Si](C)(C)OC1=CC=C(C(=O)OC2=CC(O)=CC(O[Si](C)(C)C)=C2C(=O)O)C=C1O	2881.3	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,2TMS,isomer #7	C[Si](C)(C)OC1=CC(C(=O)OC2=CC(O)=CC(O[Si](C)(C)C)=C2C(=O)O)=CC=C1O	2880.3	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,2TMS,isomer #8	C[Si](C)(C)OC1=CC(O)=C(C(=O)O)C(OC(=O)C2=CC=C(O[Si](C)(C)C)C(O)=C2)=C1	2882.0	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,2TMS,isomer #9	C[Si](C)(C)OC1=CC(O)=C(C(=O)O)C(OC(=O)C2=CC=C(O)C(O[Si](C)(C)C)=C2)=C1	2871.4	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,3TMS,isomer #1	C[Si](C)(C)OC(=O)C1=C(OC(=O)C2=CC=C(O[Si](C)(C)C)C(O)=C2)C=C(O)C=C1O[Si](C)(C)C	2857.3	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,3TMS,isomer #10	C[Si](C)(C)OC1=CC(O)=C(C(=O)O)C(OC(=O)C2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)=C1	2849.6	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,3TMS,isomer #2	C[Si](C)(C)OC(=O)C1=C(OC(=O)C2=CC=C(O)C(O[Si](C)(C)C)=C2)C=C(O)C=C1O[Si](C)(C)C	2853.8	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,3TMS,isomer #3	C[Si](C)(C)OC(=O)C1=C(OC(=O)C2=CC=C(O)C(O)=C2)C=C(O[Si](C)(C)C)C=C1O[Si](C)(C)C	2873.5	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,3TMS,isomer #4	C[Si](C)(C)OC(=O)C1=C(O)C=C(O[Si](C)(C)C)C=C1OC(=O)C1=CC=C(O[Si](C)(C)C)C(O)=C1	2891.7	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,3TMS,isomer #5	C[Si](C)(C)OC(=O)C1=C(O)C=C(O[Si](C)(C)C)C=C1OC(=O)C1=CC=C(O)C(O[Si](C)(C)C)=C1	2876.4	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,3TMS,isomer #6	C[Si](C)(C)OC(=O)C1=C(O)C=C(O)C=C1OC(=O)C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1	2842.3	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,3TMS,isomer #7	C[Si](C)(C)OC1=CC(OC(=O)C2=CC=C(O[Si](C)(C)C)C(O)=C2)=C(C(=O)O)C(O[Si](C)(C)C)=C1	2868.3	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,3TMS,isomer #8	C[Si](C)(C)OC1=CC(OC(=O)C2=CC=C(O)C(O[Si](C)(C)C)=C2)=C(C(=O)O)C(O[Si](C)(C)C)=C1	2854.4	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,3TMS,isomer #9	C[Si](C)(C)OC1=CC=C(C(=O)OC2=CC(O)=CC(O[Si](C)(C)C)=C2C(=O)O)C=C1O[Si](C)(C)C	2858.4	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,4TMS,isomer #1	C[Si](C)(C)OC(=O)C1=C(OC(=O)C2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)C=C(O)C=C1O[Si](C)(C)C	2848.8	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,4TMS,isomer #2	C[Si](C)(C)OC(=O)C1=C(OC(=O)C2=CC=C(O[Si](C)(C)C)C(O)=C2)C=C(O[Si](C)(C)C)C=C1O[Si](C)(C)C	2935.7	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,4TMS,isomer #3	C[Si](C)(C)OC(=O)C1=C(OC(=O)C2=CC=C(O)C(O[Si](C)(C)C)=C2)C=C(O[Si](C)(C)C)C=C1O[Si](C)(C)C	2917.3	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,4TMS,isomer #4	C[Si](C)(C)OC(=O)C1=C(O)C=C(O[Si](C)(C)C)C=C1OC(=O)C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1	2898.1	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,4TMS,isomer #5	C[Si](C)(C)OC1=CC(OC(=O)C2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)=C(C(=O)O)C(O[Si](C)(C)C)=C1	2888.5	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,5TMS,isomer #1	C[Si](C)(C)OC(=O)C1=C(OC(=O)C2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)C=C(O[Si](C)(C)C)C=C1O[Si](C)(C)C	2963.5	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)C1=C(O)C=C(O)C=C1OC(=O)C1=CC=C(O)C(O)=C1	3364.0	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1=CC(O)=CC(OC(=O)C2=CC=C(O)C(O)=C2)=C1C(=O)O	3285.4	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC1=CC(O)=C(C(=O)O)C(OC(=O)C2=CC=C(O)C(O)=C2)=C1	3308.7	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC1=CC(C(=O)OC2=CC(O)=CC(O)=C2C(=O)O)=CC=C1O	3297.8	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC1=CC=C(C(=O)OC2=CC(O)=CC(O)=C2C(=O)O)C=C1O	3328.3	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)C1=C(OC(=O)C2=CC=C(O)C(O)=C2)C=C(O)C=C1O[Si](C)(C)C(C)(C)C	3545.3	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC1=CC=C(C(=O)OC2=CC(O)=CC(O)=C2C(=O)O)C=C1O[Si](C)(C)C(C)(C)C	3454.1	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC(=O)C1=C(O)C=C(O[Si](C)(C)C(C)(C)C)C=C1OC(=O)C1=CC=C(O)C(O)=C1	3502.7	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC(=O)C1=C(O)C=C(O)C=C1OC(=O)C1=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C1	3493.6	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC(=O)C1=C(O)C=C(O)C=C1OC(=O)C1=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C1	3475.0	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC1=CC(OC(=O)C2=CC=C(O)C(O)=C2)=C(C(=O)O)C(O[Si](C)(C)C(C)(C)C)=C1	3477.3	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC1=CC=C(C(=O)OC2=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C2C(=O)O)C=C1O	3488.7	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC1=CC(C(=O)OC2=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C2C(=O)O)=CC=C1O	3461.9	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC1=CC(O)=C(C(=O)O)C(OC(=O)C2=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C2)=C1	3524.8	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC1=CC(O)=C(C(=O)O)C(OC(=O)C2=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C2)=C1	3492.2	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)C1=C(OC(=O)C2=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C2)C=C(O)C=C1O[Si](C)(C)C(C)(C)C	3642.5	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC1=CC(O)=C(C(=O)O)C(OC(=O)C2=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C2)=C1	3688.1	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC(=O)C1=C(OC(=O)C2=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C2)C=C(O)C=C1O[Si](C)(C)C(C)(C)C	3618.4	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC(=O)C1=C(OC(=O)C2=CC=C(O)C(O)=C2)C=C(O[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C	3601.7	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC(=O)C1=C(O)C=C(O[Si](C)(C)C(C)(C)C)C=C1OC(=O)C1=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C1	3667.6	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC(=O)C1=C(O)C=C(O[Si](C)(C)C(C)(C)C)C=C1OC(=O)C1=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C1	3638.8	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC(=O)C1=C(O)C=C(O)C=C1OC(=O)C1=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1	3578.4	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC1=CC(OC(=O)C2=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C2)=C(C(=O)O)C(O[Si](C)(C)C(C)(C)C)=C1	3737.7	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC1=CC(OC(=O)C2=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C2)=C(C(=O)O)C(O[Si](C)(C)C(C)(C)C)=C1	3713.6	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC1=CC=C(C(=O)OC2=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C2C(=O)O)C=C1O[Si](C)(C)C(C)(C)C	3635.8	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)C1=C(OC(=O)C2=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C2)C=C(O)C=C1O[Si](C)(C)C(C)(C)C	3736.6	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC(=O)C1=C(OC(=O)C2=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C2)C=C(O[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C	3830.0	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC(=O)C1=C(OC(=O)C2=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C2)C=C(O[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C	3813.0	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC(=O)C1=C(O)C=C(O[Si](C)(C)C(C)(C)C)C=C1OC(=O)C1=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1	3779.9	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC1=CC(OC(=O)C2=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C2)=C(C(=O)O)C(O[Si](C)(C)C(C)(C)C)=C1	3887.0	Semi standard non polar	33892256
2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)C1=C(OC(=O)C2=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C2)C=C(O[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C	3968.1	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 - 2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate GC-MS (Non-derivatized) - 70eV, Positive	splash10-000i-0900000000-f063a50e2100260c680c	2017-09-20	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate GC-MS (5 TMS) - 70eV, Positive	splash10-001i-0090011000-57d471b57e310ee50676	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate 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 - 2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate 10V, Positive-QTOF	splash10-052r-0596000000-47902ef3296c1477004b	2015-09-15	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate 20V, Positive-QTOF	splash10-000i-0961000000-40a68d3f3894906dba7a	2015-09-15	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate 40V, Positive-QTOF	splash10-0019-5910000000-8ede257c8c7d14f1a891	2015-09-15	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate 10V, Negative-QTOF	splash10-08fr-0194000000-f4af9d9f87266faff042	2015-09-15	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate 20V, Negative-QTOF	splash10-03di-0290000000-38a97201178b58d10cd5	2015-09-15	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate 40V, Negative-QTOF	splash10-06a0-3920000000-6ab6758b580e79a6a45d	2015-09-15	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate 10V, Positive-QTOF	splash10-000i-0692000000-5556817bba47ece0212f	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate 20V, Positive-QTOF	splash10-000i-0950000000-c9c6bed2b1d180ffeb22	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate 40V, Positive-QTOF	splash10-0f79-3930000000-ff1140404484c2ffa85f	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate 10V, Negative-QTOF	splash10-0fb9-0900000000-95ab0e687e19e8f7f0c4	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate 20V, Negative-QTOF	splash10-07gi-0970000000-2eaec82c823970bda725	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate 40V, Negative-QTOF	splash10-0fbc-3930000000-658b94bc5d3ab0cd21a8	2021-09-22	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Membrane (predicted from logP)

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

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

C04524

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

440370

PDB ID

Not Available

ChEBI ID

16068

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

Not Available

Enzymes

Enzyme Details

1. Pirin

General function:: Not Available
Specific function:: Possible transcriptional coregulator. May contribute to the regulation of cellular processes via its interaction with BCL3. May be required for efficient terminal myeloid maturation of hematopoietic cells. May play a role in the regulation of cell migration. May promote apoptosis when overexpressed. Has quercetin 2,3-dioxygenase activity (in vitro).
Gene Name:: PIR
Uniprot ID:: O00625
Molecular weight:: 32113.195

Reactions

Quercetin + Oxygen → 2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate + CO + Hydrogen Ion	details

Showing metabocard for 2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate (HMDB0059651)

MOL for HMDB0059651 (2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate)

3D MOL for HMDB0059651 (2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate)

3D SDF for HMDB0059651 (2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate)

3D-SDF for HMDB0059651 (2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate)

PDB for HMDB0059651 (2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate)

3D PDB for HMDB0059651 (2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate)

SMILES for HMDB0059651 (2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate)

INCHI for HMDB0059651 (2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate)

Structure for HMDB0059651 (2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate)

3D Structure for HMDB0059651 (2-(3,4-Dihydroxybenzoyloxy)-4,6-dihydroxybenzoate)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra

Enzymes

Reactions