MiMeDB: Showing metabocard for Luteolin (MMDBc0048026)

Not Available

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2022-04-19 21:50:00 UTC

Update Date

2024-09-27 20:08:59 UTC

Metabolite ID

MMDBc0048026

Metabolite Identification

Common Name

Luteolin

Description

Luteolin is a naturally occurring flavonoid. (PMID:17168665 ). The flavonoids are polyphenolic compounds found as integral components of the human diet. They are universally present as constituents of flowering plants, particularly of food plants. The flavonoids are phenyl substituted chromones (benzopyran derivatives) consisting of a 15-carbon basic skeleton (C6-C3-C6), composed of a chroman (C6-C3) nucleus (the benzo ring A and the heterocyclic ring C), also shared by the tocopherols, with a phenyl (the aromatic ring B) substitution usually at the 2-position. Different substitutions can typically occur in the rings, A and B. Several plants and spices containing flavonoid derivatives have found application as disease preventive and therapeutic agents in traditional medicine in Asia for thousands of years. The selection of a particular food plant, plant tissue or herb for its potential health benefits appears to mirror its flavonoid composition. The much lower risk of colon, prostate and breast cancers in Asians, who consume more vegetables, fruits and tea than populations in the Western hemisphere do, raises the question of whether flavonoid components mediate the protective effects of diets rich in these foodstuffs by acting as natural chemopreventive and anticancer agents. An impressive body of information exists on the antitumoral action of plant flavonoids. In vitro work has concentrated on the direct and indirect actions of flavonoids on tumor cells, and has found a variety of anticancer effects such as cell growth and kinase activity inhibition, apoptosis induction, suppression of the secretion of matrix metalloproteinases and of tumor invasive behavior. Furthermore, some studies have reported the impairment of in vivo angiogenesis by dietary flavonoids. Experimental animal studies indicate that certain dietary flavonoids possess antitumoral activity. The hydroxylation pattern of the B ring of the flavones and flavonols, such as luteolin seems to critically influence their activities, especially the inhibition of protein kinase activity and antiproliferation. The different mechanisms underlying the potential anticancer action of plant flavonoids await further elucidation. Certain dietary flavonols and flavones targeting cell surface signal transduction enzymes, such as protein tyrosine and focal adhesion kinases, and the processes of angiogenesis appear to be promising candidates as anticancer agents. Further in vivo studies of these bioactive constituents is deemed necessary in order to develop flavonoid-based anticancer strategies. In view of the increasing interest in the association between dietary flavonoids and cancer initiation and progression, this important field is likely to witness expanded effort and to attract and stimulate further vigorous investigations (PMID:16097445 ).

Structure

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

HMDB0005800
     RDKit          3D
Luteolin
 31 33  0  0  0  0  0  0  0  0999 V2000
    2.2961    2.3283    1.8377 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7358    1.4002    1.2245 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3499    1.4062    1.0492 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3214    0.4160    0.3855 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7781    0.4383    0.2105 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5696    1.4458    0.6954 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9558    1.4350    0.5102 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5402    0.3914   -0.1733 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9099    0.3401   -0.3799 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7676   -0.6487   -0.6796 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3948   -1.6807   -1.3619 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4150   -0.5909   -0.4714 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3947   -0.5669   -0.0949 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7067   -0.6282    0.0387 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3859   -1.7109   -0.5046 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7517   -1.7888   -0.3737 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4043   -2.8833   -0.9273 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4798   -0.8359    0.2755 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8290    0.2768    0.8400 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5661    1.2197    1.4846 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4519    0.3488    0.7042 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1558    2.2555    1.4788 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1158    2.2643    1.2309 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5328    2.2519    0.9117 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5480    1.0338   -0.0581 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9258   -2.4598   -1.7554 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8047   -1.3788   -0.8517 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8072   -2.4813   -1.0282 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7120   -2.7578   -1.9029 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5537   -0.8653    0.3970 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3107    2.0252    1.9211 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  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
  6 23  1  0
  7 24  1  0
  9 25  1  0
 11 26  1  0
 12 27  1  0
 15 28  1  0
 17 29  1  0
 18 30  1  0
 20 31  1  0
M  END


  Mrv1652309272007352D          

 21 23  0  0  0  0            999 V2000
   15.8257    2.1216    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.1103    0.4582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1091   -0.3683    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8231   -0.7806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8213    0.8703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.5359    0.4617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.5394   -0.3703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2577   -0.7810    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9774   -0.3643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9739    0.4675    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2509    0.8831    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.2600   -1.6053    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.8217   -1.6048    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.3965    0.8699    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.6861    0.8819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.4041    0.4678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.1161    0.8814    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.1139    1.7064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.3940    2.1160    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6849    1.7002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.3884    2.9401    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  2  0  0  0  0
  5  2  1  0  0  0  0
  6  7  1  0  0  0  0
  6 11  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
  8 12  2  0  0  0  0
  4 13  1  0  0  0  0
  2 14  1  0  0  0  0
 10 15  1  0  0  0  0
 15 16  2  0  0  0  0
  2  3  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
  3  4  1  0  0  0  0
 18 19  1  0  0  0  0
  4  7  2  0  0  0  0
 19 20  2  0  0  0  0
 20 15  1  0  0  0  0
 19 21  1  0  0  0  0
 18  1  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0048026

> <DATABASE_NAME>
MIME

> <SMILES>
OC1=CC(O)=C2C(=O)C=C(OC2=C1)C1=CC=C(O)C(O)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C15H10O6/c16-8-4-11(19)15-12(20)6-13(21-14(15)5-8)7-1-2-9(17)10(18)3-7/h1-6,16-19H

> <INCHI_KEY>
IQPNAANSBPBGFQ-UHFFFAOYSA-N

> <FORMULA>
C15H10O6

> <MOLECULAR_WEIGHT>
286.2363

> <EXACT_MASS>
286.047738052

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
31

> <JCHEM_AVERAGE_POLARIZABILITY>
27.727516971367624

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-chromen-4-one

> <ALOGPS_LOGP>
2.73

> <JCHEM_LOGP>
2.4031238119999996

> <ALOGPS_LOGS>
-3.32

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.069737468610946

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.574503413930256

> <JCHEM_PKA_STRONGEST_BASIC>
-5.382358240962719

> <JCHEM_POLAR_SURFACE_AREA>
107.22

> <JCHEM_REFRACTIVITY>
74.8948

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.38e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
luteolin

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0005800
     RDKit          3D
Luteolin
 31 33  0  0  0  0  0  0  0  0999 V2000
    2.2961    2.3283    1.8377 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7358    1.4002    1.2245 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3499    1.4062    1.0492 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3214    0.4160    0.3855 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7781    0.4383    0.2105 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5696    1.4458    0.6954 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9558    1.4350    0.5102 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5402    0.3914   -0.1733 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9099    0.3401   -0.3799 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7676   -0.6487   -0.6796 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3948   -1.6807   -1.3619 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4150   -0.5909   -0.4714 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3947   -0.5669   -0.0949 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7067   -0.6282    0.0387 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3859   -1.7109   -0.5046 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7517   -1.7888   -0.3737 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4043   -2.8833   -0.9273 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4798   -0.8359    0.2755 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8290    0.2768    0.8400 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5661    1.2197    1.4846 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4519    0.3488    0.7042 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1558    2.2555    1.4788 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1158    2.2643    1.2309 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5328    2.2519    0.9117 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5480    1.0338   -0.0581 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9258   -2.4598   -1.7554 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8047   -1.3788   -0.8517 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8072   -2.4813   -1.0282 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7120   -2.7578   -1.9029 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5537   -0.8653    0.3970 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3107    2.0252    1.9211 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  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
  6 23  1  0
  7 24  1  0
  9 25  1  0
 11 26  1  0
 12 27  1  0
 15 28  1  0
 17 29  1  0
 18 30  1  0
 20 31  1  0
M  END

HEADER    PROTEIN                                 27-SEP-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   27-SEP-20         0                                  
HETATM    1  O   UNK     0      29.541   3.960   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      18.873   0.855   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      18.870  -0.688   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      20.203  -1.457   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      20.200   1.625   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      21.534   0.862   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      21.540  -0.691   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      22.881  -1.458   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      24.225  -0.680   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      24.218   0.873   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      22.868   1.648   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0      22.885  -2.997   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0      20.200  -2.996   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0      17.540   1.624   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      25.547   1.646   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      26.888   0.873   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      28.217   1.645   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      28.213   3.185   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      26.869   3.950   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      25.545   3.174   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      26.858   5.488   0.000  0.00  0.00           O+0
CONECT    1   18                                                            
CONECT    2    5   14    3                                                  
CONECT    3    2    4                                                       
CONECT    4   13    3    7                                                  
CONECT    5    6    2                                                       
CONECT    6    5    7   11                                                  
CONECT    7    6    8    4                                                  
CONECT    8    7    9   12                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   15                                                  
CONECT   11    6   10                                                       
CONECT   12    8                                                            
CONECT   13    4                                                            
CONECT   14    2                                                            
CONECT   15   10   16   20                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19    1                                                  
CONECT   19   18   20   21                                                  
CONECT   20   19   15                                                       
CONECT   21   19                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   46    0
END

COMPND    HMDB0005800
HETATM    1  O1  UNL     1       2.296   2.328   1.838  1.00  0.00           O  
HETATM    2  C1  UNL     1       1.736   1.400   1.225  1.00  0.00           C  
HETATM    3  C2  UNL     1       0.350   1.406   1.049  1.00  0.00           C  
HETATM    4  C3  UNL     1      -0.321   0.416   0.385  1.00  0.00           C  
HETATM    5  C4  UNL     1      -1.778   0.438   0.211  1.00  0.00           C  
HETATM    6  C5  UNL     1      -2.570   1.446   0.695  1.00  0.00           C  
HETATM    7  C6  UNL     1      -3.956   1.435   0.510  1.00  0.00           C  
HETATM    8  C7  UNL     1      -4.540   0.391  -0.173  1.00  0.00           C  
HETATM    9  O2  UNL     1      -5.910   0.340  -0.380  1.00  0.00           O  
HETATM   10  C8  UNL     1      -3.768  -0.649  -0.680  1.00  0.00           C  
HETATM   11  O3  UNL     1      -4.395  -1.681  -1.362  1.00  0.00           O  
HETATM   12  C9  UNL     1      -2.415  -0.591  -0.471  1.00  0.00           C  
HETATM   13  O4  UNL     1       0.395  -0.567  -0.095  1.00  0.00           O  
HETATM   14  C10 UNL     1       1.707  -0.628   0.039  1.00  0.00           C  
HETATM   15  C11 UNL     1       2.386  -1.711  -0.505  1.00  0.00           C  
HETATM   16  C12 UNL     1       3.752  -1.789  -0.374  1.00  0.00           C  
HETATM   17  O5  UNL     1       4.404  -2.883  -0.927  1.00  0.00           O  
HETATM   18  C13 UNL     1       4.480  -0.836   0.276  1.00  0.00           C  
HETATM   19  C14 UNL     1       3.829   0.277   0.840  1.00  0.00           C  
HETATM   20  O6  UNL     1       4.566   1.220   1.485  1.00  0.00           O  
HETATM   21  C15 UNL     1       2.452   0.349   0.704  1.00  0.00           C  
HETATM   22  H1  UNL     1      -0.156   2.255   1.479  1.00  0.00           H  
HETATM   23  H2  UNL     1      -2.116   2.264   1.231  1.00  0.00           H  
HETATM   24  H3  UNL     1      -4.533   2.252   0.912  1.00  0.00           H  
HETATM   25  H4  UNL     1      -6.548   1.034  -0.058  1.00  0.00           H  
HETATM   26  H5  UNL     1      -3.926  -2.460  -1.755  1.00  0.00           H  
HETATM   27  H6  UNL     1      -1.805  -1.379  -0.852  1.00  0.00           H  
HETATM   28  H7  UNL     1       1.807  -2.481  -1.028  1.00  0.00           H  
HETATM   29  H8  UNL     1       4.712  -2.758  -1.903  1.00  0.00           H  
HETATM   30  H9  UNL     1       5.554  -0.865   0.397  1.00  0.00           H  
HETATM   31  H10 UNL     1       4.311   2.025   1.921  1.00  0.00           H  
CONECT    1    2    2
CONECT    2    3   21
CONECT    3    4    4   22
CONECT    4    5   13
CONECT    5    6    6   12
CONECT    6    7   23
CONECT    7    8    8   24
CONECT    8    9   10
CONECT    9   25
CONECT   10   11   12   12
CONECT   11   26
CONECT   12   27
CONECT   13   14
CONECT   14   15   15   21
CONECT   15   16   28
CONECT   16   17   18   18
CONECT   17   29
CONECT   18   19   30
CONECT   19   20   21   21
CONECT   20   31
END

HMDB0005800
     RDKit          3D
Luteolin
 31 33  0  0  0  0  0  0  0  0999 V2000
    2.2961    2.3283    1.8377 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7358    1.4002    1.2245 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3499    1.4062    1.0492 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3214    0.4160    0.3855 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7781    0.4383    0.2105 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5696    1.4458    0.6954 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9558    1.4350    0.5102 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5402    0.3914   -0.1733 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9099    0.3401   -0.3799 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7676   -0.6487   -0.6796 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3948   -1.6807   -1.3619 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4150   -0.5909   -0.4714 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3947   -0.5669   -0.0949 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7067   -0.6282    0.0387 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3859   -1.7109   -0.5046 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7517   -1.7888   -0.3737 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4043   -2.8833   -0.9273 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4798   -0.8359    0.2755 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8290    0.2768    0.8400 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5661    1.2197    1.4846 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4519    0.3488    0.7042 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1558    2.2555    1.4788 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1158    2.2643    1.2309 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5328    2.2519    0.9117 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5480    1.0338   -0.0581 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9258   -2.4598   -1.7554 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8047   -1.3788   -0.8517 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8072   -2.4813   -1.0282 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7120   -2.7578   -1.9029 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5537   -0.8653    0.3970 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3107    2.0252    1.9211 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  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
  6 23  1  0
  7 24  1  0
  9 25  1  0
 11 26  1  0
 12 27  1  0
 15 28  1  0
 17 29  1  0
 18 30  1  0
 20 31  1  0
M  END

Synonyms

Value	Source
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-benzopyrone	ChEBI
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4H-1-benzopyran-4-one	ChEBI
3',4',5,7-Tetrahydroxyflavone	ChEBI
5,7,3',4'-Tetrahydroxyflavone	ChEBI
Digitoflavone	ChEBI
Flacitran	ChEBI
Luteolol	ChEBI
Salifazide	ChEBI
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4H-benzopyrone-4-one	HMDB
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4H-chromen-4-one	HMDB
Luteoline	MeSH, HMDB
3',4',5,7-Tetrahydroxy-flavone	MeSH, HMDB
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4H-benzopyran-4-one	PhytoBank
3’,4’,5,7-Tetrahydroxyflavone	PhytoBank
5,7,3’,4’-Tetrahydroxyflavone	PhytoBank
Cyanidenon	PhytoBank

Molecular Formula

C₁₅H₁₀O₆

Average Mass

286.2363

Monoisotopic Mass

286.047738052

IUPAC Name

2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-chromen-4-one

Traditional Name

luteolin

CAS Registry Number

Not Available

SMILES

OC1=CC(O)=C2C(=O)C=C(OC2=C1)C1=CC=C(O)C(O)=C1

InChI Identifier

InChI=1S/C15H10O6/c16-8-4-11(19)15-12(20)6-13(21-14(15)5-8)7-1-2-9(17)10(18)3-7/h1-6,16-19H

InChI Key

IQPNAANSBPBGFQ-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as flavones. These are flavonoids with a structure based on the backbone of 2-phenylchromen-4-one (2-phenyl-1-benzopyran-4-one).

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Flavones

Direct Parent

Flavones

Alternative Parents

Substituents

3'-hydroxyflavonoid
4'-hydroxyflavonoid
5-hydroxyflavonoid
7-hydroxyflavonoid
Flavone
Hydroxyflavonoid
Chromone
Benzopyran
1-benzopyran
Catechol
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Pyranone
Monocyclic benzene moiety
Pyran
Benzenoid
Vinylogous acid
Heteroaromatic compound
Organoheterocyclic compound
Oxacycle
Organooxygen compound
Hydrocarbon derivative
Organic oxygen compound
Organic oxide
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

tetrahydroxyflavone (CHEBI:15864 )
3'-hydroxyflavonoid (CHEBI:15864 )
flavones (C01514 )
Flavones and Flavonols (C01514 )
Flavones and Flavonols (LMPK12110006 )

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.14 g/L	ALOGPS
logP	2.73	ALOGPS
logP	2.4	ChemAxon
logS	-3.3	ALOGPS
pKa (Strongest Acidic)	6.57	ChemAxon
pKa (Strongest Basic)	-5.4	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	107.22 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	74.89 m³·mol⁻¹	ChemAxon
Polarizability	27.73 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

Spectrum Type	Description	Splash Key	Deposition Date	View
GC-MS	GC-MS Spectrum - GC-MS (4 TMS)	splash10-0bt9-0000190000-f355e064b0e4a8fee2a8	2014-06-16	View Spectrum
GC-MS	GC-MS Spectrum - GC-MS (Non-derivatized)	splash10-0bt9-0001290000-3a6e4f4a889b4b595e3e	2014-06-16	View Spectrum
GC-MS	GC-MS Spectrum - GC-MS (Non-derivatized)	splash10-0bt9-0000190000-f355e064b0e4a8fee2a8	2017-09-12	View Spectrum
GC-MS	GC-MS Spectrum - GC-MS (Non-derivatized)	splash10-0bt9-0001290000-3a6e4f4a889b4b595e3e	2017-09-12	View Spectrum
GC-MS	GC-MS Spectrum - GC-EI-TOF (Non-derivatized)	splash10-00dj-1735900000-66504e5cc81bcf3dd0a2	2017-09-12	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positive	splash10-0aou-0290000000-c72aa0a44afb34434ad5	2017-07-27	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (4 TMS) - 70eV, Positive	splash10-0zmi-2040190000-5d0acf5ba2153f12546d	2017-10-06	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - LC-ESI-QTOF (UPLC Q-Tof Premier, Waters) , Negative	splash10-000i-0490000000-b23f87f7af1af38d9686	2012-08-31	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - LC-ESI-QTOF (UPLC Q-Tof Premier, Waters) , Negative	splash10-000i-0690000000-74dbeef56be77f266f6e	2012-08-31	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - LC-ESI-QTOF (UPLC Q-Tof Premier, Waters) 30V, Negative	splash10-001i-0900000000-4b5589ca157de0b5885b	2012-08-31	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - LC-ESI-ITTOF (LCMS-IT-TOF) , Negative	splash10-0079-0090080000-787383a28d957fc65a9e	2012-08-31	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - ESI-TOF , Negative	splash10-000i-0090000000-03ffb3e4764e7236f82d	2017-08-14	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - ESI-TOF 30V, Negative	splash10-0a4i-0190000000-7f42ffe76ed9c3f69f11	2017-08-14	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - ESI-TOF , Negative	splash10-000i-0090000000-03ffb3e4764e7236f82d	2017-09-12	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - ESI-TOF 30V, Negative	splash10-0a4i-0190000000-7f42ffe76ed9c3f69f11	2017-09-12	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - DI-ESI-qTof , Negative	splash10-000i-0790000000-814cdaf9d50189cf2f2a	2017-09-14	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - LC-ESI-QTOF , negative	splash10-000i-0490000000-b23f87f7af1af38d9686	2017-09-14	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - LC-ESI-QTOF , negative	splash10-000i-0690000000-4135ff68dafc65e9f339	2017-09-14	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - LC-ESI-QTOF , negative	splash10-001i-0900000000-4b5589ca157de0b5885b	2017-09-14	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - LC-ESI-QTOF , negative	splash10-000i-0090000000-568d5c1e3df3c5693fb4	2017-09-14	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - LC-ESI-QTOF , negative	splash10-000i-0190000000-b20ef421e6accd0523a4	2017-09-14	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - LC-ESI-QTOF , negative	splash10-001i-0900000000-2ca1121832520dd96a2c	2017-09-14	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - Linear Ion Trap , negative	splash10-0006-0490000000-14b50e413340dc95fac3	2017-09-14	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - Linear Ion Trap , negative	splash10-0006-0490000000-371552bb5776fd662dd9	2017-09-14	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - Linear Ion Trap , negative	splash10-0006-0590000000-a412d0980f838bf49619	2017-09-14	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - Linear Ion Trap , negative	splash10-000i-0090000000-075f1c69f8e77ea5dbe9	2017-09-14	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - LC-ESI-TOF , negative	splash10-0a4i-0190000000-7f42ffe76ed9c3f69f11	2017-09-14	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - 10V, Negative	splash10-000i-0090000000-236ab0853a3df459fc37	2021-09-20	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - 40V, Negative	splash10-001i-0900000000-fda1f09c1506187911ff	2021-09-20	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - 20V, Negative	splash10-000i-0190000000-956ceb8d223bd9454f93	2021-09-20	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - 40V, Negative	splash10-001i-1900000000-ba91f3571fdd8398c5e9	2021-09-20	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - 50V, Negative	splash10-001i-0900000000-051f4eceea0c40ddb177	2021-09-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CD₃OD, experimental)		2012-12-05	View Spectrum
2D NMR	[¹H, ¹³C]-HSQC NMR Spectrum (2D, 600 MHz, CD₃OD, experimental)		2012-12-05	View Spectrum

Biological Properties

Cellular Locations

Membrane

Biospecimen Locations

Blood
Feces
Urine

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
MMDBp0191942	Catechol O-methyltransferase	Unknown	P21964	Homo sapiens
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

Multistep Reactions

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference
MMDBr0012762	Luteolin	4-Hydroxycinnamic acid	Not Available			Manually annotated by MiMeDB team
MMDBr0012805	4-Vinylphenol	4-Ethylphenol	Not Available	vinyl phenol reductase

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Evidence Type	Host and Biospecimen	Data Source	Reference
Neuroprotective		Animal_model	Rat	PubMed	31362009

Microbial Sources

Superkingdom/Kingdom	Phylum	Total species	Hosts and Body Sites
Eukaryota/Fungi	Basidiomycota	8	Human feces
Eukaryota/Fungi	Ascomycota	2
Bacteria	Proteobacteria	1

Exposure Sources

Source Type	Species	Data Source	Reference
Plant	Parsley	FooDB	Not Available
Plant	Peppermint	FooDB	Not Available
Plant	Broccoli	FooDB	Not Available
Plant	Oregano	FooDB	Not Available
Plant	Red bell pepper	FooDB	Not Available
Plant	Anise	FooDB	Not Available
Plant	Thyme	FooDB	Not Available
Plant	Cumin	FooDB	Not Available
Plant	Common juniper	FooDB	Not Available
Plant	Celery	FooDB	Not Available

Source Type	Activity	Data Source	Reference
Not Available	Antioxidant	U.S. Environmental Protection Agency	CompTox
General Exposome	Not Available	U.S. Environmental Protection Agency	CompTox
Drugs	Antimicrobial	U.S. Environmental Protection Agency	CompTox
Cosmetics	Not Available	U.S. Environmental Protection Agency	CompTox
Domestics	Not Available	U.S. Environmental Protection Agency	CompTox
Cosmetics	Not Available	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
Human Blood	Detected and Quantified			0	0.288	uM	Adult (>18 years old)	Both	Normal	HMDB	19747418
Human Blood	Detected and Quantified	0.0999	0.0977			uM	Adult (>18 years old)	Both	Normal	HMDB	19747418
Human Blood	Detected and Quantified	0.101	0.0985			uM	Adult (>18 years old)	Both	Normal	HMDB	20851305
Human Feces	Detected but not Quantified						Adult (>18 years old)	Both	Normal	HMDB	25037050
Human Urine	Detected but not Quantified						Adult (>18 years old)	Both	Normal	HMDB	32966057
Human Blood	Detected but not Quantified						Adult (>18 years old)	Both	Normal	HMDB	32966057

External Links

HMDB ID

HMDB0005800

DrugBank ID

Not Available

Phenol Explorer Compound ID

FooDB ID

KNApSAcK ID

Chemspider ID

KEGG Compound ID

BioCyc ID

5734-TETRAHYDROXYFLAVONE

BiGG ID

Not Available

Wikipedia Link

Luteolin

METLIN ID

Not Available

PubChem Compound

5280445

PDB ID

LU2

ChEBI ID

15864

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

General References

Kandaswami C, Lee LT, Lee PP, Hwang JJ, Ke FC, Huang YT, Lee MT: The antitumor activities of flavonoids. In Vivo. 2005 Sep-Oct;19(5):895-909. [PubMed:16097445 ]
Lupu R, Menendez JA: Pharmacological inhibitors of Fatty Acid Synthase (FASN)--catalyzed endogenous fatty acid biogenesis: a new family of anti-cancer agents? Curr Pharm Biotechnol. 2006 Dec;7(6):483-93. doi: 10.2174/138920106779116928. [PubMed:17168665 ]

Showing metabocard for Luteolin (MMDBc0048026)

MOL for #<Metabolite:0x00007fdb5962e648>

3D MOL for #<Metabolite:0x00007fdb5962e648>

3D SDF for #<Metabolite:0x00007fdb5962e648>

3D-SDF for #<Metabolite:0x00007fdb5962e648>

PDB for #<Metabolite:0x00007fdb5962e648>

3D PDB for #<Metabolite:0x00007fdb5962e648>

SMILES for #<Metabolite:0x00007fdb5962e648>

INCHI for #<Metabolite:0x00007fdb5962e648>

Structure for #<Metabolite:0x00007fdb5962e648>

3D Structure for #<Metabolite:0x00007fdb5962e648>