MiMeDB: Showing metabocard for Liquiritigenin (MMDBc0053420)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2022-05-16 21:24:05 UTC

Update Date

2024-10-10 01:15:46 UTC

Metabolite ID

MMDBc0053420

Metabolite Identification

Common Name

Liquiritigenin

Description

Liquiritigenin is found in alfalfa. Liquiritigenin is isolated from Glycyrrhiza, Medicago, Myroxylon, Cicer, and all Leguminosae species. Several glycosides, particularly rutinoside and neohesperidoside, are important in influencing citrus fruit flavour.

Structure

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

HMDB0029519
     RDKit          3D
Liquiritigenin
 31 33  0  0  0  0  0  0  0  0999 V2000
   -2.0132   -3.0820    0.0328 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5112   -1.9439   -0.1019 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0539   -1.7840   -0.2527 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3951   -0.6672    0.6344 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7946   -0.2656    0.3217 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3190    0.9105    0.8276 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6214    1.3051    0.5492 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4026    0.5000   -0.2507 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7113    0.8056   -0.5856 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8930   -0.6881   -0.7697 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5861   -1.0623   -0.4771 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4118    0.4661    0.4767 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7630    0.4456    0.1877 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5615    1.5812    0.1818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8966    1.5474   -0.1056 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6479    2.7130   -0.0972 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4513    0.3215   -0.3989 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7162   -0.8432   -0.4105 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3578   -0.7628   -0.1116 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4981   -2.7144    0.0233 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1623   -1.4951   -1.3030 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3517   -0.9699    1.7187 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6938    1.5407    1.4591 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0592    2.2131    0.9266 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9421    1.3538   -1.4222 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5044   -1.3214   -1.3976 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2295   -1.9947   -0.9017 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0688    2.5121    0.4197 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0805    2.9685    0.7863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5109    0.2261   -0.6368 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1195   -1.8159   -0.6354 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  2  0
  4 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 15 17  2  0
 17 18  1  0
 18 19  2  0
 19  2  1  0
 11  5  1  0
 19 13  1  0
  3 20  1  0
  3 21  1  0
  4 22  1  1
  6 23  1  0
  7 24  1  0
  9 25  1  0
 10 26  1  0
 11 27  1  0
 14 28  1  0
 16 29  1  0
 17 30  1  0
 18 31  1  0
M  END


  Mrv1652309042000362D          

 20 22  0  0  1  0            999 V2000
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -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
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    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
    5.0013   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    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
    4.2868    0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    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
    4.2868   -0.8250    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  3  1  1  0  0  0  0
  4  2  2  0  0  0  0
  6  5  2  0  0  0  0
  9  1  2  0  0  0  0
  9  2  1  0  0  0  0
 10  3  2  0  0  0  0
 10  4  1  0  0  0  0
 11  5  1  0  0  0  0
 11  7  2  0  0  0  0
 12  6  1  0  0  0  0
 13  8  1  0  0  0  0
 13 12  1  0  0  0  0
 14  8  1  0  0  0  0
 14  9  1  1  0  0  0
 15  7  1  0  0  0  0
 15 12  2  0  0  0  0
 16 10  1  0  0  0  0
 17 11  1  0  0  0  0
 18 13  2  0  0  0  0
 19 14  1  0  0  0  0
 19 15  1  0  0  0  0
 14 20  1  6  0  0  0
M  END
> <DATABASE_ID>
MMDBc0053420

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@]1(CC(=O)C2=C(O1)C=C(O)C=C2)C1=CC=C(O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C15H12O4/c16-10-3-1-9(2-4-10)14-8-13(18)12-6-5-11(17)7-15(12)19-14/h1-7,14,16-17H,8H2/t14-/m0/s1

> <INCHI_KEY>
FURUXTVZLHCCNA-AWEZNQCLSA-N

> <FORMULA>
C15H12O4

> <MOLECULAR_WEIGHT>
256.2534

> <EXACT_MASS>
256.073558872

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
31

> <JCHEM_AVERAGE_POLARIZABILITY>
26.413284948640513

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S)-7-hydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-4-one

> <ALOGPS_LOGP>
2.79

> <JCHEM_LOGP>
2.4886733719999996

> <ALOGPS_LOGS>
-3.28

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.480776938340991

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.788865277012675

> <JCHEM_PKA_STRONGEST_BASIC>
-4.939949525645975

> <JCHEM_POLAR_SURFACE_AREA>
66.76

> <JCHEM_REFRACTIVITY>
69.30890000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.33e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-deoxyflavanone

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0029519
     RDKit          3D
Liquiritigenin
 31 33  0  0  0  0  0  0  0  0999 V2000
   -2.0132   -3.0820    0.0328 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5112   -1.9439   -0.1019 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0539   -1.7840   -0.2527 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3951   -0.6672    0.6344 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7946   -0.2656    0.3217 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3190    0.9105    0.8276 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6214    1.3051    0.5492 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4026    0.5000   -0.2507 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7113    0.8056   -0.5856 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8930   -0.6881   -0.7697 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5861   -1.0623   -0.4771 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4118    0.4661    0.4767 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7630    0.4456    0.1877 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5615    1.5812    0.1818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8966    1.5474   -0.1056 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6479    2.7130   -0.0972 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4513    0.3215   -0.3989 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7162   -0.8432   -0.4105 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3578   -0.7628   -0.1116 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4981   -2.7144    0.0233 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1623   -1.4951   -1.3030 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3517   -0.9699    1.7187 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6938    1.5407    1.4591 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0592    2.2131    0.9266 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9421    1.3538   -1.4222 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5044   -1.3214   -1.3976 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2295   -1.9947   -0.9017 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0688    2.5121    0.4197 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0805    2.9685    0.7863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5109    0.2261   -0.6368 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1195   -1.8159   -0.6354 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  2  0
  4 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 15 17  2  0
 17 18  1  0
 18 19  2  0
 19  2  1  0
 11  5  1  0
 19 13  1  0
  3 20  1  0
  3 21  1  0
  4 22  1  1
  6 23  1  0
  7 24  1  0
  9 25  1  0
 10 26  1  0
 11 27  1  0
 14 28  1  0
 16 29  1  0
 17 30  1  0
 18 31  1  0
M  END

HEADER    PROTEIN                                 04-SEP-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-20         0                                  
HETATM    1  C   UNK     0       9.336  -2.310   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.669   0.000   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      10.669  -3.080   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      12.003  -0.770   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.336  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      12.003  -2.310   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.002   0.000   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      13.337  -3.080   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       1.334  -0.770   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0       6.668   3.850   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       6.668  -0.770   0.000  0.00  0.00           O+0
HETATM   20  H   UNK     0       8.002  -1.540   0.000  0.00  0.00           H+0
CONECT    1    3    9                                                       
CONECT    2    4    9                                                       
CONECT    3    1   10                                                       
CONECT    4    2   10                                                       
CONECT    5    6   11                                                       
CONECT    6    5   12                                                       
CONECT    7   11   15                                                       
CONECT    8   13   14                                                       
CONECT    9    1    2   14                                                  
CONECT   10    3    4   16                                                  
CONECT   11    5    7   17                                                  
CONECT   12    6   13   15                                                  
CONECT   13    8   12   18                                                  
CONECT   14    8    9   19   20                                             
CONECT   15    7   12   19                                                  
CONECT   16   10                                                            
CONECT   17   11                                                            
CONECT   18   13                                                            
CONECT   19   14   15                                                       
CONECT   20   14                                                            
MASTER        0    0    0    0    0    0    0    0   20    0   44    0
END

COMPND    HMDB0029519
HETATM    1  O1  UNL     1      -2.013  -3.082   0.033  1.00  0.00           O  
HETATM    2  C1  UNL     1      -1.511  -1.944  -0.102  1.00  0.00           C  
HETATM    3  C2  UNL     1      -0.054  -1.784  -0.253  1.00  0.00           C  
HETATM    4  C3  UNL     1       0.395  -0.667   0.634  1.00  0.00           C  
HETATM    5  C4  UNL     1       1.795  -0.266   0.322  1.00  0.00           C  
HETATM    6  C5  UNL     1       2.319   0.911   0.828  1.00  0.00           C  
HETATM    7  C6  UNL     1       3.621   1.305   0.549  1.00  0.00           C  
HETATM    8  C7  UNL     1       4.403   0.500  -0.251  1.00  0.00           C  
HETATM    9  O2  UNL     1       5.711   0.806  -0.586  1.00  0.00           O  
HETATM   10  C8  UNL     1       3.893  -0.688  -0.770  1.00  0.00           C  
HETATM   11  C9  UNL     1       2.586  -1.062  -0.477  1.00  0.00           C  
HETATM   12  O3  UNL     1      -0.412   0.466   0.477  1.00  0.00           O  
HETATM   13  C10 UNL     1      -1.763   0.446   0.188  1.00  0.00           C  
HETATM   14  C11 UNL     1      -2.562   1.581   0.182  1.00  0.00           C  
HETATM   15  C12 UNL     1      -3.897   1.547  -0.106  1.00  0.00           C  
HETATM   16  O4  UNL     1      -4.648   2.713  -0.097  1.00  0.00           O  
HETATM   17  C13 UNL     1      -4.451   0.322  -0.399  1.00  0.00           C  
HETATM   18  C14 UNL     1      -3.716  -0.843  -0.411  1.00  0.00           C  
HETATM   19  C15 UNL     1      -2.358  -0.763  -0.112  1.00  0.00           C  
HETATM   20  H1  UNL     1       0.498  -2.714   0.023  1.00  0.00           H  
HETATM   21  H2  UNL     1       0.162  -1.495  -1.303  1.00  0.00           H  
HETATM   22  H3  UNL     1       0.352  -0.970   1.719  1.00  0.00           H  
HETATM   23  H4  UNL     1       1.694   1.541   1.459  1.00  0.00           H  
HETATM   24  H5  UNL     1       4.059   2.213   0.927  1.00  0.00           H  
HETATM   25  H6  UNL     1       5.942   1.354  -1.422  1.00  0.00           H  
HETATM   26  H7  UNL     1       4.504  -1.321  -1.398  1.00  0.00           H  
HETATM   27  H8  UNL     1       2.230  -1.995  -0.902  1.00  0.00           H  
HETATM   28  H9  UNL     1      -2.069   2.512   0.420  1.00  0.00           H  
HETATM   29  H10 UNL     1      -5.080   2.969   0.786  1.00  0.00           H  
HETATM   30  H11 UNL     1      -5.511   0.226  -0.637  1.00  0.00           H  
HETATM   31  H12 UNL     1      -4.119  -1.816  -0.635  1.00  0.00           H  
CONECT    1    2    2
CONECT    2    3   19
CONECT    3    4   20   21
CONECT    4    5   12   22
CONECT    5    6    6   11
CONECT    6    7   23
CONECT    7    8    8   24
CONECT    8    9   10
CONECT    9   25
CONECT   10   11   11   26
CONECT   11   27
CONECT   12   13
CONECT   13   14   14   19
CONECT   14   15   28
CONECT   15   16   17   17
CONECT   16   29
CONECT   17   18   30
CONECT   18   19   19   31
END

HMDB0029519
     RDKit          3D
Liquiritigenin
 31 33  0  0  0  0  0  0  0  0999 V2000
   -2.0132   -3.0820    0.0328 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5112   -1.9439   -0.1019 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0539   -1.7840   -0.2527 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3951   -0.6672    0.6344 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7946   -0.2656    0.3217 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3190    0.9105    0.8276 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6214    1.3051    0.5492 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4026    0.5000   -0.2507 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7113    0.8056   -0.5856 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8930   -0.6881   -0.7697 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5861   -1.0623   -0.4771 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4118    0.4661    0.4767 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7630    0.4456    0.1877 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5615    1.5812    0.1818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8966    1.5474   -0.1056 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6479    2.7130   -0.0972 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4513    0.3215   -0.3989 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7162   -0.8432   -0.4105 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3578   -0.7628   -0.1116 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4981   -2.7144    0.0233 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1623   -1.4951   -1.3030 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3517   -0.9699    1.7187 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6938    1.5407    1.4591 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0592    2.2131    0.9266 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9421    1.3538   -1.4222 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5044   -1.3214   -1.3976 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2295   -1.9947   -0.9017 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0688    2.5121    0.4197 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0805    2.9685    0.7863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5109    0.2261   -0.6368 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1195   -1.8159   -0.6354 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  2  0
  4 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 15 17  2  0
 17 18  1  0
 18 19  2  0
 19  2  1  0
 11  5  1  0
 19 13  1  0
  3 20  1  0
  3 21  1  0
  4 22  1  1
  6 23  1  0
  7 24  1  0
  9 25  1  0
 10 26  1  0
 11 27  1  0
 14 28  1  0
 16 29  1  0
 17 30  1  0
 18 31  1  0
M  END

Synonyms

Value	Source
(-)-Liquiritigenin	ChEBI
(2S)-7-Hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-1-benzopyran-4-one	ChEBI
(2S)-Liquiritigenin	ChEBI
4',7-Dihydroxyflavanone	ChEBI
7,4'-Dihydroxyflavanone	ChEBI
(-)-(2S)-7,4'-Dihydroxyflavanone	HMDB
(-)-(2S)-7,4’-Dihydroxyflavanone	HMDB
(-)-(S)-4',7-Dihydroxyflavanone	HMDB
(-)-(S)-4’,7-Dihydroxyflavanone	HMDB
(2S)-2,3-Dihydro-7-hydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one	HMDB
(2S)-7-Hydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one	HMDB
4’,7-Dihydroxyflavanone	HMDB
7,4’-Dihydroxyflavanone	HMDB
Liquiritigenin	HMDB
5-Deoxyflavanone	HMDB
DFV	HMDB

Molecular Formula

C₁₅H₁₂O₄

Average Mass

256.2534

Monoisotopic Mass

256.073558872

IUPAC Name

(2S)-7-hydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-4-one

Traditional Name

5-deoxyflavanone

CAS Registry Number

Not Available

SMILES

[H][C@]1(CC(=O)C2=C(O1)C=C(O)C=C2)C1=CC=C(O)C=C1

InChI Identifier

InChI=1S/C15H12O4/c16-10-3-1-9(2-4-10)14-8-13(18)12-6-5-11(17)7-15(12)19-14/h1-7,14,16-17H,8H2/t14-/m0/s1

InChI Key

FURUXTVZLHCCNA-AWEZNQCLSA-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

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

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

dihydroxyflavanone (CHEBI:28777 )
flavanones (C09762 )
Flavanones (LMPK12140061 )

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.13 g/L	ALOGPS
logP	2.79	ALOGPS
logP	2.49	ChemAxon
logS	-3.3	ALOGPS
pKa (Strongest Acidic)	7.79	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	66.76 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	69.31 m³·mol⁻¹	ChemAxon
Polarizability	26.41 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

Membrane

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Protein ID	Protein Name	Protein Type	Uniprot ID	Species

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
Eukaryota/Fungi	Basidiomycota	8	Human feces
Eukaryota/Fungi	Ascomycota	2

Exposure Sources

Other Exposures

Source Type	Data Source	Reference
Drugs - Antimicrobial	U.S. Environmental Protection Agency	CompTox
Cosmetics	U.S. Environmental Protection Agency	CompTox
Domestics	U.S. Environmental Protection Agency	CompTox
Cosmetics	U.S. Environmental Protection Agency	CompTox

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Units	Age	Sex	Health Condition	Data Source	Reference

External Links

HMDB ID

HMDB0029519

DrugBank ID

DB03601

Phenol Explorer Compound ID

Not Available

FooDB ID

KNApSAcK ID

Chemspider ID

KEGG Compound ID

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Liquiritigenin

METLIN ID

Not Available

PubChem Compound

114829

PDB ID

Not Available

ChEBI ID

28777

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

General References

Wishart DS, Li C, Marcu A, Badran H, Pon A, Budinski Z, Patron J, Lipton D, Cao X, Oler E, Li K, Paccoud M, Hong C, Guo AC, Chan C, Wei W, Ramirez-Gaona M: PathBank: a comprehensive pathway database for model organisms. Nucleic Acids Res. 2020 Jan 8;48(D1):D470-D478. doi: 10.1093/nar/gkz861. [PubMed:31602464 ]
Yannai, Shmuel (2004). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. Boca Raton: Chapman & Hall/CRC..

Showing metabocard for Liquiritigenin (MMDBc0053420)

MOL for #<Metabolite:0x00007f920228a0c8>

3D MOL for #<Metabolite:0x00007f920228a0c8>

3D SDF for #<Metabolite:0x00007f920228a0c8>

3D-SDF for #<Metabolite:0x00007f920228a0c8>

PDB for #<Metabolite:0x00007f920228a0c8>

3D PDB for #<Metabolite:0x00007f920228a0c8>

SMILES for #<Metabolite:0x00007f920228a0c8>

INCHI for #<Metabolite:0x00007f920228a0c8>

Structure for #<Metabolite:0x00007f920228a0c8>

3D Structure for #<Metabolite:0x00007f920228a0c8>