MiMeDB: Showing metabocard for Eriodictyol (MMDBc0000611)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2020-12-10 18:51:05 UTC

Update Date

2024-09-27 20:46:06 UTC

Metabolite ID

MMDBc0000611

Metabolite Identification

Common Name

Eriodictyol

Description

Eriodictyol, also known as 3',4',5,7-tetrahydroxyflavanone or 2,3-dihydroluteolin, belongs to the class of organic compounds known as flavanones. Flavanones are compounds containing a flavan-3-one moiety, with a structure characterized by a 2-phenyl-3,4-dihydro-2H-1-benzopyran bearing a ketone at the carbon C3. Thus, eriodictyol is considered to be a flavonoid lipid molecule. Outside of the human body, eriodictyol has been detected, but not quantified in, several different foods, such as common oregano, common thymes, parsley, sweet basils, and tarragons. This could make eriodictyol a potential biomarker for the consumption of these foods. Eriodictyol is a compound isolated from Eriodictyon californicum and can be used in medicine as an expectorant. BioTransformer predicts that eriodictiol is a product of luteolin metabolism via a flavonoid-c-ring-reduction reaction catalyzed by an unspecified-gut microbiota enzyme (PMID: 30612223 ).

Structure

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

HMDB0005810
     RDKit          3D
Eriodictyol
 33 35  0  0  0  0  0  0  0  0999 V2000
   -1.9544   -0.5904   -2.7699 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5421   -0.1145   -1.7191 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1303    0.3334   -1.4866 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2948   -0.4546   -0.2442 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7284   -0.4530   -0.0389 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4734   -1.5691   -0.3418 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8442   -1.6140   -0.1624 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5006   -0.4899    0.3437 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8795   -0.5682    0.5121 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7733    0.6178    0.6461 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4171    1.7405    1.1499 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3854    0.6430    0.4570 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4482    0.0884    0.8223 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8274    0.1503    0.6906 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6493    0.3092    1.8027 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0158    0.3694    1.6640 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8632    0.5296    2.7772 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5834    0.2729    0.4215 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7918    0.1117   -0.7303 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3541    0.0183   -1.9566 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4456    0.0551   -0.5635 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1805    1.3979   -1.1909 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5148    0.1308   -2.3443 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1127   -1.4985   -0.3925 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0052   -2.4679   -0.7384 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3856   -2.5231   -0.4184 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4715    0.1523    0.8610 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3911    1.8048    1.3127 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8885    1.5470    0.7175 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1807    0.3852    2.7909 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1340    1.4513    3.1061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6535    0.3175    0.2888 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0862   -0.0830   -2.8664 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 10 12  2  0
  4 13  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 16 18  2  0
 18 19  1  0
 19 20  1  0
 19 21  2  0
 21  2  1  0
 12  5  1  0
 21 14  1  0
  3 22  1  0
  3 23  1  0
  4 24  1  6
  6 25  1  0
  7 26  1  0
  9 27  1  0
 11 28  1  0
 12 29  1  0
 15 30  1  0
 17 31  1  0
 18 32  1  0
 20 33  1  0
M  END


  Mrv1652307102016272D          

 21 23  0  0  0  0            999 V2000
    1.0716    1.4437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7861    1.8562    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7861    0.2062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5007   -0.6187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7862    0.6187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3572   -0.6187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0716    0.6187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5007    0.2062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5005    1.4437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5005    0.6187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7862   -1.0312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3572   -1.0312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3572    0.2062    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0717    0.2062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0717   -0.6187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2151    0.6187    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2151    1.8562    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7862   -1.8562    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3572   -1.8562    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3572    0.6187    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1924    0.1694    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0  0  0  0
  7  1  2  0  0  0  0
  7  3  1  0  0  0  0
  8  4  2  0  0  0  0
  8  5  1  0  0  0  0
  9  2  2  0  0  0  0
 10  3  2  0  0  0  0
 10  9  1  0  0  0  0
 11  4  1  0  0  0  0
 12  6  1  0  0  0  0
 13  6  1  0  0  0  0
 13  7  1  6  0  0  0
 14  5  2  0  0  0  0
 15 11  2  0  0  0  0
 15 12  1  0  0  0  0
 15 14  1  0  0  0  0
 16  8  1  0  0  0  0
 17  9  1  0  0  0  0
 18 11  1  0  0  0  0
 19 12  2  0  0  0  0
 20 13  1  0  0  0  0
 20 14  1  0  0  0  0
 10 21  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0000611

> <DATABASE_NAME>
MIME

> <SMILES>
OC1=CC(O)=C2C(=O)C[C@H](OC2=C1)C1=CC=C(O)C(O)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C15H12O6/c16-8-4-11(19)15-12(20)6-13(21-14(15)5-8)7-1-2-9(17)10(18)3-7/h1-5,13,16-19H,6H2/t13-/m0/s1

> <INCHI_KEY>
SBHXYTNGIZCORC-ZDUSSCGKSA-N

> <FORMULA>
C15H12O6

> <MOLECULAR_WEIGHT>
288.2522

> <EXACT_MASS>
288.063388116

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
33

> <JCHEM_AVERAGE_POLARIZABILITY>
27.326042752894896

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2H-1-benzopyran-4-one

> <ALOGPS_LOGP>
2.15

> <JCHEM_LOGP>
2.5315427286666665

> <ALOGPS_LOGS>
-2.90

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.053712609058154

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.847641206936137

> <JCHEM_PKA_STRONGEST_BASIC>
-4.950235552435861

> <JCHEM_POLAR_SURFACE_AREA>
107.22000000000001

> <JCHEM_REFRACTIVITY>
73.27069999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.66e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
eriodictyol

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0005810
     RDKit          3D
Eriodictyol
 33 35  0  0  0  0  0  0  0  0999 V2000
   -1.9544   -0.5904   -2.7699 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5421   -0.1145   -1.7191 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1303    0.3334   -1.4866 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2948   -0.4546   -0.2442 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7284   -0.4530   -0.0389 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4734   -1.5691   -0.3418 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8442   -1.6140   -0.1624 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5006   -0.4899    0.3437 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8795   -0.5682    0.5121 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7733    0.6178    0.6461 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4171    1.7405    1.1499 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3854    0.6430    0.4570 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4482    0.0884    0.8223 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8274    0.1503    0.6906 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6493    0.3092    1.8027 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0158    0.3694    1.6640 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8632    0.5296    2.7772 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5834    0.2729    0.4215 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7918    0.1117   -0.7303 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3541    0.0183   -1.9566 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4456    0.0551   -0.5635 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1805    1.3979   -1.1909 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5148    0.1308   -2.3443 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1127   -1.4985   -0.3925 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0052   -2.4679   -0.7384 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3856   -2.5231   -0.4184 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4715    0.1523    0.8610 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3911    1.8048    1.3127 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8885    1.5470    0.7175 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1807    0.3852    2.7909 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1340    1.4513    3.1061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6535    0.3175    0.2888 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0862   -0.0830   -2.8664 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 10 12  2  0
  4 13  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 16 18  2  0
 18 19  1  0
 19 20  1  0
 19 21  2  0
 21  2  1  0
 12  5  1  0
 21 14  1  0
  3 22  1  0
  3 23  1  0
  4 24  1  6
  6 25  1  0
  7 26  1  0
  9 27  1  0
 11 28  1  0
 12 29  1  0
 15 30  1  0
 17 31  1  0
 18 32  1  0
 20 33  1  0
M  END

HEADER    PROTEIN                                 10-JUL-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-JUL-20         0                                  
HETATM    1  C   UNK     0       2.000   2.695   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.334   3.465   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.334   0.385   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.668  -1.155   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -3.334   1.155   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.667  -1.155   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.000   1.155   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -4.668   0.385   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.668   2.695   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.668   1.155   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -3.334  -1.925   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.667  -1.925   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.667   0.385   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.001   0.385   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.001  -1.155   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -6.002   1.155   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       6.002   3.465   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0      -3.334  -3.465   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0      -0.667  -3.465   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      -0.667   1.155   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       5.959   0.316   0.000  0.00  0.00           O+0
CONECT    1    2    7                                                       
CONECT    2    1    9                                                       
CONECT    3    7   10                                                       
CONECT    4    8   11                                                       
CONECT    5    8   14                                                       
CONECT    6   12   13                                                       
CONECT    7    1    3   13                                                  
CONECT    8    4    5   16                                                  
CONECT    9    2   10   17                                                  
CONECT   10    3    9   21                                                  
CONECT   11    4   15   18                                                  
CONECT   12    6   15   19                                                  
CONECT   13    6    7   20                                                  
CONECT   14    5   15   20                                                  
CONECT   15   11   12   14                                                  
CONECT   16    8                                                            
CONECT   17    9                                                            
CONECT   18   11                                                            
CONECT   19   12                                                            
CONECT   20   13   14                                                       
CONECT   21   10                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   46    0
END

COMPND    HMDB0005810
HETATM    1  O1  UNL     1      -1.954  -0.590  -2.770  1.00  0.00           O  
HETATM    2  C1  UNL     1      -1.542  -0.114  -1.719  1.00  0.00           C  
HETATM    3  C2  UNL     1      -0.130   0.333  -1.487  1.00  0.00           C  
HETATM    4  C3  UNL     1       0.295  -0.455  -0.244  1.00  0.00           C  
HETATM    5  C4  UNL     1       1.728  -0.453  -0.039  1.00  0.00           C  
HETATM    6  C5  UNL     1       2.473  -1.569  -0.342  1.00  0.00           C  
HETATM    7  C6  UNL     1       3.844  -1.614  -0.162  1.00  0.00           C  
HETATM    8  C7  UNL     1       4.501  -0.490   0.344  1.00  0.00           C  
HETATM    9  O2  UNL     1       5.880  -0.568   0.512  1.00  0.00           O  
HETATM   10  C8  UNL     1       3.773   0.618   0.646  1.00  0.00           C  
HETATM   11  O3  UNL     1       4.417   1.740   1.150  1.00  0.00           O  
HETATM   12  C9  UNL     1       2.385   0.643   0.457  1.00  0.00           C  
HETATM   13  O4  UNL     1      -0.448   0.088   0.822  1.00  0.00           O  
HETATM   14  C10 UNL     1      -1.827   0.150   0.691  1.00  0.00           C  
HETATM   15  C11 UNL     1      -2.649   0.309   1.803  1.00  0.00           C  
HETATM   16  C12 UNL     1      -4.016   0.369   1.664  1.00  0.00           C  
HETATM   17  O5  UNL     1      -4.863   0.530   2.777  1.00  0.00           O  
HETATM   18  C13 UNL     1      -4.583   0.273   0.422  1.00  0.00           C  
HETATM   19  C14 UNL     1      -3.792   0.112  -0.730  1.00  0.00           C  
HETATM   20  O6  UNL     1      -4.354   0.018  -1.957  1.00  0.00           O  
HETATM   21  C15 UNL     1      -2.446   0.055  -0.563  1.00  0.00           C  
HETATM   22  H1  UNL     1      -0.181   1.398  -1.191  1.00  0.00           H  
HETATM   23  H2  UNL     1       0.515   0.131  -2.344  1.00  0.00           H  
HETATM   24  H3  UNL     1      -0.113  -1.499  -0.392  1.00  0.00           H  
HETATM   25  H4  UNL     1       2.005  -2.468  -0.738  1.00  0.00           H  
HETATM   26  H5  UNL     1       4.386  -2.523  -0.418  1.00  0.00           H  
HETATM   27  H6  UNL     1       6.472   0.152   0.861  1.00  0.00           H  
HETATM   28  H7  UNL     1       5.391   1.805   1.313  1.00  0.00           H  
HETATM   29  H8  UNL     1       1.889   1.547   0.718  1.00  0.00           H  
HETATM   30  H9  UNL     1      -2.181   0.385   2.791  1.00  0.00           H  
HETATM   31  H10 UNL     1      -5.134   1.451   3.106  1.00  0.00           H  
HETATM   32  H11 UNL     1      -5.654   0.317   0.289  1.00  0.00           H  
HETATM   33  H12 UNL     1      -4.086  -0.083  -2.866  1.00  0.00           H  
CONECT    1    2    2
CONECT    2    3   21
CONECT    3    4   22   23
CONECT    4    5   13   24
CONECT    5    6    6   12
CONECT    6    7   25
CONECT    7    8    8   26
CONECT    8    9   10
CONECT    9   27
CONECT   10   11   12   12
CONECT   11   28
CONECT   12   29
CONECT   13   14
CONECT   14   15   15   21
CONECT   15   16   30
CONECT   16   17   18   18
CONECT   17   31
CONECT   18   19   32
CONECT   19   20   21   21
CONECT   20   33
END

HMDB0005810
     RDKit          3D
Eriodictyol
 33 35  0  0  0  0  0  0  0  0999 V2000
   -1.9544   -0.5904   -2.7699 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5421   -0.1145   -1.7191 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1303    0.3334   -1.4866 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2948   -0.4546   -0.2442 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7284   -0.4530   -0.0389 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4734   -1.5691   -0.3418 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8442   -1.6140   -0.1624 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5006   -0.4899    0.3437 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8795   -0.5682    0.5121 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7733    0.6178    0.6461 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4171    1.7405    1.1499 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3854    0.6430    0.4570 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4482    0.0884    0.8223 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8274    0.1503    0.6906 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6493    0.3092    1.8027 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0158    0.3694    1.6640 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8632    0.5296    2.7772 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5834    0.2729    0.4215 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7918    0.1117   -0.7303 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3541    0.0183   -1.9566 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4456    0.0551   -0.5635 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1805    1.3979   -1.1909 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5148    0.1308   -2.3443 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1127   -1.4985   -0.3925 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0052   -2.4679   -0.7384 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3856   -2.5231   -0.4184 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4715    0.1523    0.8610 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3911    1.8048    1.3127 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8885    1.5470    0.7175 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1807    0.3852    2.7909 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1340    1.4513    3.1061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6535    0.3175    0.2888 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0862   -0.0830   -2.8664 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 10 12  2  0
  4 13  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 16 18  2  0
 18 19  1  0
 19 20  1  0
 19 21  2  0
 21  2  1  0
 12  5  1  0
 21 14  1  0
  3 22  1  0
  3 23  1  0
  4 24  1  6
  6 25  1  0
  7 26  1  0
  9 27  1  0
 11 28  1  0
 12 29  1  0
 15 30  1  0
 17 31  1  0
 18 32  1  0
 20 33  1  0
M  END

Synonyms

Value	Source
(S)-2-(3,4-Dihydroxyphenyl)-2,3-dihydro-5,7-dihydroxy-4-benzopyrone	ChEBI
(S)-Eriodictyol	ChEBI
Eriodictiol	ChEBI
(+)-Eriodictyol	HMDB
(2S)-Eriodictyol	HMDB
(S)-2,3-Dihydroluteolin	HMDB
(S)-3',4',5,7-Tetrahydroxyflavanone	HMDB
(S)-3’,4’,5,7-Tetrahydroxyflavanone	HMDB
3',4',5,7-Tetrahydroxyflavanone	HMDB
3’,4’,5,7-Tetrahydroxyflavanone	HMDB
(2S)-2-(3,4-Dihydroxyphenyl)-2,3-dihydro-5,7-dihydroxy-4H-1-benzopyran-4-one	HMDB
(2S)-2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-2,3-dihydrochromen-4-one	HMDB
Huazhongilexone	HMDB

Molecular Formula

C₁₅H₁₂O₆

Average Mass

288.2522

Monoisotopic Mass

288.063388116

IUPAC Name

(2S)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2H-1-benzopyran-4-one

Traditional Name

eriodictyol

CAS Registry Number

Not Available

SMILES

OC1=CC(O)=C2C(=O)C[C@H](OC2=C1)C1=CC=C(O)C(O)=C1

InChI Identifier

InChI=1S/C15H12O6/c16-8-4-11(19)15-12(20)6-13(21-14(15)5-8)7-1-2-9(17)10(18)3-7/h1-5,13,16-19H,6H2/t13-/m0/s1

InChI Key

SBHXYTNGIZCORC-ZDUSSCGKSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as flavanones. Flavanones are compounds containing a flavan-3-one moiety, with a structure characterized by a 2-phenyl-3,4-dihydro-2H-1-benzopyran bearing a ketone at the carbon C3.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Flavans

Direct Parent

Flavanones

Alternative Parents

Substituents

Flavanone
3'-hydroxyflavonoid
4'-hydroxyflavonoid
5-hydroxyflavonoid
7-hydroxyflavonoid
Hydroxyflavonoid
Chromone
Benzopyran
Chromane
1-benzopyran
Catechol
Aryl ketone
Aryl alkyl ketone
1-hydroxy-2-unsubstituted benzenoid
Phenol
1-hydroxy-4-unsubstituted benzenoid
Alkyl aryl ether
Benzenoid
Monocyclic benzene moiety
Vinylogous acid
Ketone
Organoheterocyclic compound
Oxacycle
Ether
Organooxygen compound
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

3'-hydroxyflavanones (CHEBI:28412 )
tetrahydroxyflavanone (CHEBI:28412 )
flavanones (C05631 )
Flavanones (LMPK12140002 )

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.37 g/L	ALOGPS
logP	2.15	ALOGPS
logP	2.53	ChemAxon
logS	-2.9	ALOGPS
pKa (Strongest Acidic)	7.85	ChemAxon
pKa (Strongest Basic)	-5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	107.22 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	73.27 m³·mol⁻¹	ChemAxon
Polarizability	27.33 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Not Available

Biological Properties

Cellular Locations

Cytoplasm
Membrane

Biospecimen Locations

Blood
Feces
Kidney
Liver
Urine

Tissue Locations

Kidney
Liver

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Protein ID	Protein Name	Protein Type	Uniprot ID	Species
MMDBp0192140	UDP-glucuronosyltransferase 1-1	Enzyme	P22309	Homo sapiens
MMDBp0197061	Sulfotransferase 1A3	Enzyme	P0DMM9	Homo sapiens

Human Pathways

Pathways

Name	SMPDB/PathBank

Metabolic Reactions

Reactions

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Evidence Type	Host and Biospecimen	Data Source	Reference

Microbial Sources

Superkingdom/Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
Bacteria/Eubacteria	Verrucomicrobia	1	Human feces; Human stool; Human ; Human urine	Indirect association between microbiota composition and metabolites measured in host biospecimen
Bacteria/Eubacteria	Actinobacteria	1	Human vaginal fluid; Human feces	Indirect association between microbiota composition and metabolites measured in host biospecimen
Bacteria/Eubacteria	Firmicutes	1	Human feces	Indirect association between microbiota composition and metabolites measured in host biospecimen

Exposure Sources

Other Exposures

Source Type	Data Source	Reference
General Exposome	U.S. Environmental Protection Agency	CompTox
Cosmetics	U.S. Environmental Protection Agency	CompTox
Domestics	U.S. Environmental Protection Agency	CompTox
Food Additive	U.S. Food and Drug Administration	FDA

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Units	Age	Sex	Health Condition	Data Source	Reference
Human Urine	Detected and Quantified	0.000694	umol/mmol creatinine	Adult (>18 years old)	Both	Normal	HMDB	20683461
Human Urine	Detected and Quantified	0.00393	umol/mmol creatinine	Adult (>18 years old)	Both	Normal	HMDB	20683461
Human Urine	Detected and Quantified	0.00555	umol/mmol creatinine	Adult (>18 years old)	Both	Normal	HMDB	20683461
Human Urine	Detected and Quantified	0.00733	umol/mmol creatinine	Adult (>18 years old)	Both	Normal	HMDB	21272408
Human Kidney	Detected but not Quantified			Not Specified	Not Specified	Normal	HMDB	34986597
Human Liver	Detected but not Quantified			Not Specified	Not Specified	Normal	HMDB	34986597
Human Feces	Detected but not Quantified			Adult (>18 years old)	Both	Normal	HMDB	25037050
Human Blood	Detected but not Quantified						HMDB

External Links

HMDB ID

HMDB0005810

DrugBank ID

Not Available

Phenol Explorer Compound ID

FooDB ID

KNApSAcK ID

Chemspider ID

KEGG Compound ID

BioCyc ID

BiGG ID

Not Available

Wikipedia Link

Eriodictyol

METLIN ID

3415

PubChem Compound

440735

PDB ID

Not Available

ChEBI ID

28412

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

General References

'T Hart BA, Ip Via Ching TR, Van Dijk H, Labadie RP: How flavonoids inhibit the generation of luminol-dependent chemiluminescence by activated human neutrophils. Chem Biol Interact. 1990;73(2-3):323-35. doi: 10.1016/0009-2797(90)90012-c. [PubMed:2155715 ]
Ogata S, Miyake Y, Yamamoto K, Okumura K, Taguchi H: Apoptosis induced by the flavonoid from lemon fruit (Citrus limon BURM. f.) and its metabolites in HL-60 cells. Biosci Biotechnol Biochem. 2000 May;64(5):1075-8. doi: 10.1271/bbb.64.1075. [PubMed:10879486 ]
Miyake Y, Sakurai C, Usuda M, Fukumoto S, Hiramitsu M, Sakaida K, Osawa T, Kondo K: Difference in plasma metabolite concentration after ingestion of lemon flavonoids and their aglycones in humans. J Nutr Sci Vitaminol (Tokyo). 2006 Feb;52(1):54-60. doi: 10.3177/jnsv.52.54. [PubMed:16637230 ]
Djoumbou-Feunang Y, Fiamoncini J, Gil-de-la-Fuente A, Greiner R, Manach C, Wishart DS: BioTransformer: a comprehensive computational tool for small molecule metabolism prediction and metabolite identification. J Cheminform. 2019 Jan 5;11(1):2. doi: 10.1186/s13321-018-0324-5. [PubMed:30612223 ]

Showing metabocard for Eriodictyol (MMDBc0000611)

MOL for #<Metabolite:0x00007f923c31ad28>

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3D PDB for #<Metabolite:0x00007f923c31ad28>

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Structure for #<Metabolite:0x00007f923c31ad28>

3D Structure for #<Metabolite:0x00007f923c31ad28>