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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-12 02:32:37 UTC

Update Date

2022-03-07 02:56:48 UTC

HMDB ID

HMDB0040930

Secondary Accession Numbers

HMDB40930

Metabolite Identification

Common Name

1,5-Bis(4-hydroxy-3-methoxyphenyl)-1,4-pentadien-3-one

Description

1,5-Bis(4-hydroxy-3-methoxyphenyl)-1,4-pentadien-3-one belongs to the class of organic compounds known as hydroxycinnamic acids and derivatives. Hydroxycinnamic acids and derivatives are compounds containing an cinnamic acid (or a derivative thereof) where the benzene ring is hydroxylated. 1,5-Bis(4-hydroxy-3-methoxyphenyl)-1,4-pentadien-3-one has been detected, but not quantified in, herbs and spices and turmerics (Curcuma longa). This could make 1,5-bis(4-hydroxy-3-methoxyphenyl)-1,4-pentadien-3-one a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on 1,5-Bis(4-hydroxy-3-methoxyphenyl)-1,4-pentadien-3-one.

Structure

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

HMDB0040930
     RDKit          3D
1,5-Bis(4-hydroxy-3-methoxyphenyl)-1,4-pentadien-3-one
 42 43  0  0  0  0  0  0  0  0999 V2000
    6.1376   -1.2633   -1.4339 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5532   -1.5706   -0.1864 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4565   -0.8742    0.3156 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8870    0.1432   -0.3721 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7672    0.8847    0.0965 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3583    2.0332   -0.6478 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1852    2.4436   -0.9212 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0244    1.7542   -0.5171 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0457    0.6696    0.0516 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2654    2.4314   -0.8437 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4417    2.0722   -0.5390 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8703    0.9422    0.2107 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2761    0.3273    1.2576 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7573   -0.8648    1.8370 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8922   -1.4645    1.3417 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4109   -2.6394    1.8735 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5200   -0.8648    0.2841 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.8804   -0.5503    2.0203 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.0644   -1.5928   -1.7977 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5399    0.7438   -1.0885 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4714    1.0527    1.8276 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4374   -0.8039    2.9970 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv0541 05061312152D          

 24 25  0  0  0  0            999 V2000
   -4.2868    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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 13  3  1  0  0  0  0
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 23 18  1  0  0  0  0
 24  2  1  0  0  0  0
 24 19  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0040930

> <DATABASE_NAME>
hmdb

> <SMILES>
COC1=C(O)C=CC(\C=C/C(=O)/C=C\C2=CC(OC)=C(O)C=C2)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C19H18O5/c1-23-18-11-13(5-9-16(18)21)3-7-15(20)8-4-14-6-10-17(22)19(12-14)24-2/h3-12,21-22H,1-2H3/b7-3-,8-4-

> <INCHI_KEY>
ISIMGBQRFXXNON-VHOZIDCHSA-N

> <FORMULA>
C19H18O5

> <MOLECULAR_WEIGHT>
326.3432

> <EXACT_MASS>
326.115423686

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_AVERAGE_POLARIZABILITY>
33.49817870695116

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1Z,4Z)-1,5-bis(4-hydroxy-3-methoxyphenyl)penta-1,4-dien-3-one

> <ALOGPS_LOGP>
3.31

> <JCHEM_LOGP>
3.902670582333333

> <ALOGPS_LOGS>
-4.79

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.805976591295552

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.20391659940859

> <JCHEM_PKA_STRONGEST_BASIC>
-4.331575407940574

> <JCHEM_POLAR_SURFACE_AREA>
75.99000000000001

> <JCHEM_REFRACTIVITY>
93.91539999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.33e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1Z,4Z)-1,5-bis(4-hydroxy-3-methoxyphenyl)penta-1,4-dien-3-one

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0040930
     RDKit          3D
1,5-Bis(4-hydroxy-3-methoxyphenyl)-1,4-pentadien-3-one
 42 43  0  0  0  0  0  0  0  0999 V2000
    6.1376   -1.2633   -1.4339 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5532   -1.5706   -0.1864 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4565   -0.8742    0.3156 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8870    0.1432   -0.3721 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7672    0.8847    0.0965 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3583    2.0332   -0.6478 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1852    2.4436   -0.9212 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0244    1.7542   -0.5171 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0457    0.6696    0.0516 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2654    2.4314   -0.8437 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4417    2.0722   -0.5390 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8703    0.9422    0.2107 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2761    0.3273    1.2576 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7573   -0.8648    1.8370 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8922   -1.4645    1.3417 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4109   -2.6394    1.8735 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5200   -0.8648    0.2841 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6772   -1.4546   -0.2361 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3736   -0.8857   -1.3292 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0378    0.2919   -0.2673 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2898    0.4967    1.3227 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8804   -0.5503    2.0203 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9593   -1.2506    1.5442 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5204   -2.2952    2.2787 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1469   -1.6960   -1.5234 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.1638    3.3788   -1.4338 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2658    2.7696   -0.9273 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4315    0.7597    1.7787 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2563   -1.3237    2.6643 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9361   -3.0711    2.6554 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8314    0.0784   -1.0754 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5912   -0.6688   -2.1144 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0644   -1.5928   -1.7977 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5399    0.7438   -1.0885 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4714    1.0527    1.8276 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4374   -0.8039    2.9970 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3146   -2.7703    1.8703 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
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 10 11  2  0
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 23  3  1  0
 20 12  1  0
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 20 39  1  0
 21 40  1  0
 22 41  1  0
 24 42  1  0
M  END

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0      -8.002   6.160   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -5.335   0.000   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -4.001   2.310   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      -4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -4.001   3.850   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -6.668   2.310   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -5.335   1.540   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.667   0.000   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -5.335   4.620   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -6.668   3.850   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -1.334  -0.770   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      -5.335   6.160   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       4.001  -0.770   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      -8.002   4.620   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       4.001   2.310   0.000  0.00  0.00           O+0
CONECT    1   23                                                            
CONECT    2   24                                                            
CONECT    3    7   13                                                       
CONECT    4    8   14                                                       
CONECT    5    9   13                                                       
CONECT    6   10   14                                                       
CONECT    7    3   15                                                       
CONECT    8    4   15                                                       
CONECT    9    5   16                                                       
CONECT   10    6   17                                                       
CONECT   11   13   18                                                       
CONECT   12   14   19                                                       
CONECT   13    3    5   11                                                  
CONECT   14    4    6   12                                                  
CONECT   15    7    8   20                                                  
CONECT   16    9   18   21                                                  
CONECT   17   10   19   22                                                  
CONECT   18   11   16   23                                                  
CONECT   19   12   17   24                                                  
CONECT   20   15                                                            
CONECT   21   16                                                            
CONECT   22   17                                                            
CONECT   23    1   18                                                       
CONECT   24    2   19                                                       
MASTER        0    0    0    0    0    0    0    0   24    0   50    0
END

COMPND    HMDB0040930
HETATM    1  C1  UNL     1       6.138  -1.263  -1.434  1.00  0.00           C  
HETATM    2  O1  UNL     1       5.553  -1.571  -0.186  1.00  0.00           O  
HETATM    3  C2  UNL     1       4.457  -0.874   0.316  1.00  0.00           C  
HETATM    4  C3  UNL     1       3.887   0.143  -0.372  1.00  0.00           C  
HETATM    5  C4  UNL     1       2.767   0.885   0.097  1.00  0.00           C  
HETATM    6  C5  UNL     1       2.358   2.033  -0.648  1.00  0.00           C  
HETATM    7  C6  UNL     1       1.185   2.444  -0.921  1.00  0.00           C  
HETATM    8  C7  UNL     1      -0.024   1.754  -0.517  1.00  0.00           C  
HETATM    9  O2  UNL     1       0.046   0.670   0.052  1.00  0.00           O  
HETATM   10  C8  UNL     1      -1.265   2.431  -0.844  1.00  0.00           C  
HETATM   11  C9  UNL     1      -2.442   2.072  -0.539  1.00  0.00           C  
HETATM   12  C10 UNL     1      -2.870   0.942   0.211  1.00  0.00           C  
HETATM   13  C11 UNL     1      -2.276   0.327   1.258  1.00  0.00           C  
HETATM   14  C12 UNL     1      -2.757  -0.865   1.837  1.00  0.00           C  
HETATM   15  C13 UNL     1      -3.892  -1.464   1.342  1.00  0.00           C  
HETATM   16  O3  UNL     1      -4.411  -2.639   1.873  1.00  0.00           O  
HETATM   17  C14 UNL     1      -4.520  -0.865   0.284  1.00  0.00           C  
HETATM   18  O4  UNL     1      -5.677  -1.455  -0.236  1.00  0.00           O  
HETATM   19  C15 UNL     1      -6.374  -0.886  -1.329  1.00  0.00           C  
HETATM   20  C16 UNL     1      -4.038   0.292  -0.267  1.00  0.00           C  
HETATM   21  C17 UNL     1       2.290   0.497   1.323  1.00  0.00           C  
HETATM   22  C18 UNL     1       2.880  -0.550   2.020  1.00  0.00           C  
HETATM   23  C19 UNL     1       3.959  -1.251   1.544  1.00  0.00           C  
HETATM   24  O5  UNL     1       4.520  -2.295   2.279  1.00  0.00           O  
HETATM   25  H1  UNL     1       7.147  -1.696  -1.523  1.00  0.00           H  
HETATM   26  H2  UNL     1       6.204  -0.168  -1.622  1.00  0.00           H  
HETATM   27  H3  UNL     1       5.500  -1.698  -2.221  1.00  0.00           H  
HETATM   28  H4  UNL     1       4.281   0.449  -1.357  1.00  0.00           H  
HETATM   29  H5  UNL     1       3.203   2.665  -1.048  1.00  0.00           H  
HETATM   30  H6  UNL     1       1.029   3.383  -1.504  1.00  0.00           H  
HETATM   31  H7  UNL     1      -1.164   3.379  -1.434  1.00  0.00           H  
HETATM   32  H8  UNL     1      -3.266   2.770  -0.927  1.00  0.00           H  
HETATM   33  H9  UNL     1      -1.432   0.760   1.779  1.00  0.00           H  
HETATM   34  H10 UNL     1      -2.256  -1.324   2.664  1.00  0.00           H  
HETATM   35  H11 UNL     1      -3.936  -3.071   2.655  1.00  0.00           H  
HETATM   36  H12 UNL     1      -6.831   0.078  -1.075  1.00  0.00           H  
HETATM   37  H13 UNL     1      -5.591  -0.669  -2.114  1.00  0.00           H  
HETATM   38  H14 UNL     1      -7.064  -1.593  -1.798  1.00  0.00           H  
HETATM   39  H15 UNL     1      -4.540   0.744  -1.088  1.00  0.00           H  
HETATM   40  H16 UNL     1       1.471   1.053   1.828  1.00  0.00           H  
HETATM   41  H17 UNL     1       2.437  -0.804   2.997  1.00  0.00           H  
HETATM   42  H18 UNL     1       5.315  -2.770   1.870  1.00  0.00           H  
CONECT    1    2   25   26   27
CONECT    2    3
CONECT    3    4    4   23
CONECT    4    5   28
CONECT    5    6   21   21
CONECT    6    7    7   29
CONECT    7    8   30
CONECT    8    9    9   10
CONECT   10   11   11   31
CONECT   11   12   32
CONECT   12   13   13   20
CONECT   13   14   33
CONECT   14   15   15   34
CONECT   15   16   17
CONECT   16   35
CONECT   17   18   20   20
CONECT   18   19
CONECT   19   36   37   38
CONECT   20   39
CONECT   21   22   40
CONECT   22   23   23   41
CONECT   23   24
CONECT   24   42
END

HMDB0040930
     RDKit          3D
1,5-Bis(4-hydroxy-3-methoxyphenyl)-1,4-pentadien-3-one
 42 43  0  0  0  0  0  0  0  0999 V2000
    6.1376   -1.2633   -1.4339 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5532   -1.5706   -0.1864 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4565   -0.8742    0.3156 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8870    0.1432   -0.3721 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7672    0.8847    0.0965 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3583    2.0332   -0.6478 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1852    2.4436   -0.9212 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0244    1.7542   -0.5171 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0457    0.6696    0.0516 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2654    2.4314   -0.8437 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4417    2.0722   -0.5390 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8703    0.9422    0.2107 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2761    0.3273    1.2576 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7573   -0.8648    1.8370 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8922   -1.4645    1.3417 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4109   -2.6394    1.8735 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5200   -0.8648    0.2841 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6772   -1.4546   -0.2361 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3736   -0.8857   -1.3292 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0378    0.2919   -0.2673 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2898    0.4967    1.3227 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8804   -0.5503    2.0203 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9593   -1.2506    1.5442 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5204   -2.2952    2.2787 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1469   -1.6960   -1.5234 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2042   -0.1676   -1.6223 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4998   -1.6976   -2.2214 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2808    0.4491   -1.3574 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2029    2.6649   -1.0483 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0285    3.3826   -1.5045 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1638    3.3788   -1.4338 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2658    2.7696   -0.9273 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4315    0.7597    1.7787 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2563   -1.3237    2.6643 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9361   -3.0711    2.6554 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8314    0.0784   -1.0754 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5912   -0.6688   -2.1144 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0644   -1.5928   -1.7977 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5399    0.7438   -1.0885 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4714    1.0527    1.8276 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4374   -0.8039    2.9970 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3146   -2.7703    1.8703 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 18 19  1  0
 17 20  2  0
  5 21  2  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 23  3  1  0
 20 12  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  4 28  1  0
  6 29  1  0
  7 30  1  0
 10 31  1  0
 11 32  1  0
 13 33  1  0
 14 34  1  0
 16 35  1  0
 19 36  1  0
 19 37  1  0
 19 38  1  0
 20 39  1  0
 21 40  1  0
 22 41  1  0
 24 42  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
1,5-Bis(4-hydroxy-3-methoxyphenyl)-1,4-pentadien-3-one, 9ci	HMDB
Hylin	MeSH
1,5-Bis(4-hydroxy-3-methoxyphenyl)-1,4-pentadien-3-one	MeSH

Chemical Formula

C₁₉H₁₈O₅

Average Molecular Weight

326.3432

Monoisotopic Molecular Weight

326.115423686

IUPAC Name

(1Z,4Z)-1,5-bis(4-hydroxy-3-methoxyphenyl)penta-1,4-dien-3-one

Traditional Name

(1Z,4Z)-1,5-bis(4-hydroxy-3-methoxyphenyl)penta-1,4-dien-3-one

CAS Registry Number

131359-25-6

SMILES

COC1=C(O)C=CC(\C=C/C(=O)/C=C\C2=CC(OC)=C(O)C=C2)=C1

InChI Identifier

InChI=1S/C19H18O5/c1-23-18-11-13(5-9-16(18)21)3-7-15(20)8-4-14-6-10-17(22)19(12-14)24-2/h3-12,21-22H,1-2H3/b7-3-,8-4-

InChI Key

ISIMGBQRFXXNON-VHOZIDCHSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hydroxycinnamic acids and derivatives. Hydroxycinnamic acids and derivatives are compounds containing an cinnamic acid (or a derivative thereof) where the benzene ring is hydroxylated.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Cinnamic acids and derivatives

Sub Class

Hydroxycinnamic acids and derivatives

Direct Parent

Hydroxycinnamic acids and derivatives

Alternative Parents

Substituents

Hydroxycinnamic acid or derivatives
Methoxyphenol
Phenoxy compound
Phenol ether
Styrene
Methoxybenzene
Anisole
Phenol
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Benzenoid
Monocyclic benzene moiety
Enone
Alpha,beta-unsaturated ketone
Acryloyl-group
Ketone
Ether
Organic oxygen compound
Carbonyl group
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cell membrane (HMDB: HMDB0040930)

Cellular substructure

Membrane (HMDB: HMDB0040930)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0040930)

Source

Exogenous

Food

Food (HMDB: HMDB0040930)

Herb and spice

Spice

Turmeric (FooDB: FOOD00068)

Herbs and Spices (FooDB: FOOD00866)

Endogenous

Plant

Plant (HMDB: HMDB0040930)

Process

Not Available

Role

Biological role

anti Alzheimeran (HMDB: HMDB0040930)
anti amyloid-beta (HMDB: HMDB0040930)

Nutrient

Nutrient (HMDB: HMDB0040930)

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	82 - 83 °C	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	0.0053 g/L	ALOGPS
logP	3.31	ALOGPS
logP	3.9	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	9.2	ChemAxon
pKa (Strongest Basic)	-4.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	75.99 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	93.92 m³·mol⁻¹	ChemAxon
Polarizability	33.5 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
DeepCCS	[M+H]+	185.975	30932474
DeepCCS	[M-H]-	183.617	30932474
DeepCCS	[M-2H]-	217.824	30932474
DeepCCS	[M+Na]+	193.409	30932474
AllCCS	[M+H]+	179.6	32859911
AllCCS	[M+H-H2O]+	176.0	32859911
AllCCS	[M+NH4]+	182.9	32859911
AllCCS	[M+Na]+	183.8	32859911
AllCCS	[M-H]-	178.0	32859911
AllCCS	[M+Na-2H]-	177.9	32859911
AllCCS	[M+HCOO]-	177.9	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
1,5-Bis(4-hydroxy-3-methoxyphenyl)-1,4-pentadien-3-one	COC1=C(O)C=CC(\C=C/C(=O)/C=C\C2=CC(OC)=C(O)C=C2)=C1	5583.4	Standard polar	33892256
1,5-Bis(4-hydroxy-3-methoxyphenyl)-1,4-pentadien-3-one	COC1=C(O)C=CC(\C=C/C(=O)/C=C\C2=CC(OC)=C(O)C=C2)=C1	3064.7	Standard non polar	33892256
1,5-Bis(4-hydroxy-3-methoxyphenyl)-1,4-pentadien-3-one	COC1=C(O)C=CC(\C=C/C(=O)/C=C\C2=CC(OC)=C(O)C=C2)=C1	3337.5	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
1,5-Bis(4-hydroxy-3-methoxyphenyl)-1,4-pentadien-3-one,1TMS,isomer #1	COC1=CC(/C=C\C(=O)/C=C\C2=CC=C(O[Si](C)(C)C)C(OC)=C2)=CC=C1O	3336.5	Semi standard non polar	33892256
1,5-Bis(4-hydroxy-3-methoxyphenyl)-1,4-pentadien-3-one,2TMS,isomer #1	COC1=CC(/C=C\C(=O)/C=C\C2=CC=C(O[Si](C)(C)C)C(OC)=C2)=CC=C1O[Si](C)(C)C	3350.2	Semi standard non polar	33892256
1,5-Bis(4-hydroxy-3-methoxyphenyl)-1,4-pentadien-3-one,1TBDMS,isomer #1	COC1=CC(/C=C\C(=O)/C=C\C2=CC=C(O[Si](C)(C)C(C)(C)C)C(OC)=C2)=CC=C1O	3614.9	Semi standard non polar	33892256
1,5-Bis(4-hydroxy-3-methoxyphenyl)-1,4-pentadien-3-one,2TBDMS,isomer #1	COC1=CC(/C=C\C(=O)/C=C\C2=CC=C(O[Si](C)(C)C(C)(C)C)C(OC)=C2)=CC=C1O[Si](C)(C)C(C)(C)C	3901.3	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 - 1,5-Bis(4-hydroxy-3-methoxyphenyl)-1,4-pentadien-3-one GC-MS (Non-derivatized) - 70eV, Positive	splash10-002b-0915000000-991c67ffe767dbeef180	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 1,5-Bis(4-hydroxy-3-methoxyphenyl)-1,4-pentadien-3-one GC-MS (2 TMS) - 70eV, Positive	splash10-0ab9-3062900000-9ee72abf96edc4513d33	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 1,5-Bis(4-hydroxy-3-methoxyphenyl)-1,4-pentadien-3-one 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 - 1,5-Bis(4-hydroxy-3-methoxyphenyl)-1,4-pentadien-3-one 10V, Positive-QTOF	splash10-004i-0209000000-2326cd3c68abcf720a69	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1,5-Bis(4-hydroxy-3-methoxyphenyl)-1,4-pentadien-3-one 20V, Positive-QTOF	splash10-002s-0923000000-99edbe4926e301790a86	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1,5-Bis(4-hydroxy-3-methoxyphenyl)-1,4-pentadien-3-one 40V, Positive-QTOF	splash10-059i-1920000000-8d2ac84a6665134c85fe	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1,5-Bis(4-hydroxy-3-methoxyphenyl)-1,4-pentadien-3-one 10V, Negative-QTOF	splash10-004i-0109000000-b68da4adac0aad76de64	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1,5-Bis(4-hydroxy-3-methoxyphenyl)-1,4-pentadien-3-one 20V, Negative-QTOF	splash10-004i-0519000000-e28c6c4cc4c9043d6e15	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1,5-Bis(4-hydroxy-3-methoxyphenyl)-1,4-pentadien-3-one 40V, Negative-QTOF	splash10-0040-0791000000-800bdc6ec2d911b0b8d3	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1,5-Bis(4-hydroxy-3-methoxyphenyl)-1,4-pentadien-3-one 10V, Positive-QTOF	splash10-004i-0029000000-e11b43f3987e33b270a2	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1,5-Bis(4-hydroxy-3-methoxyphenyl)-1,4-pentadien-3-one 20V, Positive-QTOF	splash10-004j-0892000000-e8f6452c7c47b7a2c5b1	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1,5-Bis(4-hydroxy-3-methoxyphenyl)-1,4-pentadien-3-one 40V, Positive-QTOF	splash10-056s-1930000000-47d570a745c006cc98b2	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1,5-Bis(4-hydroxy-3-methoxyphenyl)-1,4-pentadien-3-one 10V, Negative-QTOF	splash10-004i-0009000000-765e63f069b5c07fc717	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1,5-Bis(4-hydroxy-3-methoxyphenyl)-1,4-pentadien-3-one 20V, Negative-QTOF	splash10-00di-0977000000-d5d86ae960f484372979	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1,5-Bis(4-hydroxy-3-methoxyphenyl)-1,4-pentadien-3-one 40V, Negative-QTOF	splash10-0fl1-0292000000-18b9e3097cc47b1aa950	2021-09-22	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Membrane

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

FDB020771

KNApSAcK ID

C00055462

Chemspider ID

30777523

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

131752986

PDB ID

Not Available

ChEBI ID

175163

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

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

Showing metabocard for 1,5-Bis(4-hydroxy-3-methoxyphenyl)-1,4-pentadien-3-one (HMDB0040930)

MOL for HMDB0040930 (1,5-Bis(4-hydroxy-3-methoxyphenyl)-1,4-pentadien-3-one)

3D MOL for HMDB0040930 (1,5-Bis(4-hydroxy-3-methoxyphenyl)-1,4-pentadien-3-one)

3D SDF for HMDB0040930 (1,5-Bis(4-hydroxy-3-methoxyphenyl)-1,4-pentadien-3-one)

3D-SDF for HMDB0040930 (1,5-Bis(4-hydroxy-3-methoxyphenyl)-1,4-pentadien-3-one)

PDB for HMDB0040930 (1,5-Bis(4-hydroxy-3-methoxyphenyl)-1,4-pentadien-3-one)

3D PDB for HMDB0040930 (1,5-Bis(4-hydroxy-3-methoxyphenyl)-1,4-pentadien-3-one)

SMILES for HMDB0040930 (1,5-Bis(4-hydroxy-3-methoxyphenyl)-1,4-pentadien-3-one)

INCHI for HMDB0040930 (1,5-Bis(4-hydroxy-3-methoxyphenyl)-1,4-pentadien-3-one)

Structure for HMDB0040930 (1,5-Bis(4-hydroxy-3-methoxyphenyl)-1,4-pentadien-3-one)

3D Structure for HMDB0040930 (1,5-Bis(4-hydroxy-3-methoxyphenyl)-1,4-pentadien-3-one)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra