MiMeDB: Showing metabocard for Phenethyl hexanoate (MMDBc0047745)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-11-19 15:40:42 UTC

Update Date

2025-01-16 05:03:10 UTC

Metabolite ID

MMDBc0047745

Metabolite Identification

Common Name

Phenethyl hexanoate

Description

2-Phenylethyl hexanoate is found in alcoholic beverages. 2-Phenylethyl hexanoate is found in alcoholic drinks, fruit juices and other natural sources. 2-Phenylethyl hexanoate is a food flavour.

Structure

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

HMDB0037718
     RDKit          3D
2-Phenylethyl hexanoate
 36 36  0  0  0  0  0  0  0  0999 V2000
   -5.0708    0.9644   -0.2521 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3948   -0.3542    0.3374 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5705   -1.4875   -0.1059 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1387   -1.5110    0.2005 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3279   -0.3826   -0.3515 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8815   -0.6097    0.0055 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5749   -1.6212    0.6581 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1157    0.2717   -0.3700 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4602    0.0067   -0.0058 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2969    1.1557   -0.5660 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7095    0.8864   -0.1888 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4967    0.1396   -1.0688 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8111   -0.1584   -0.8044 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3892    0.2858    0.3626 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6096    1.0254    1.2339 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2846    1.3305    0.9761 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4887    0.8547   -1.1695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0270    1.4840   -0.6111 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6131    1.6521    0.4765 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5030   -0.5553    0.1718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2926   -0.2409    1.4652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0566   -2.4258    0.3081 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6902   -1.6162   -1.2238 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6997   -2.4573   -0.2288 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9759   -1.6124    1.3166 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6356    0.5658    0.1469 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4478   -0.3532   -1.4432 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5971   -0.0145    1.0989 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8483   -0.9165   -0.4360 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1828    1.1206   -1.6598 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9862    2.1297   -0.1257 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0406   -0.2078   -1.9840 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4220   -0.7344   -1.4808 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4039    0.0899    0.6291 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0318    1.3933    2.1658 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7034    1.9028    1.6640 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 11  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  2 20  1  0
  2 21  1  0
  3 22  1  0
  3 23  1  0
  4 24  1  0
  4 25  1  0
  5 26  1  0
  5 27  1  0
  9 28  1  0
  9 29  1  0
 10 30  1  0
 10 31  1  0
 12 32  1  0
 13 33  1  0
 14 34  1  0
 15 35  1  0
 16 36  1  0
M  END


  Mrv0541 05061309582D          

 16 16  0  0  0  0            999 V2000
    2.8579    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0  0  0  0
  3  2  1  0  0  0  0
  5  3  1  0  0  0  0
  6  4  2  0  0  0  0
  7  4  1  0  0  0  0
  8  6  1  0  0  0  0
  9  7  2  0  0  0  0
 10  5  1  0  0  0  0
 12 11  1  0  0  0  0
 13  8  2  0  0  0  0
 13  9  1  0  0  0  0
 13 11  1  0  0  0  0
 14 10  1  0  0  0  0
 15 14  2  0  0  0  0
 16 12  1  0  0  0  0
 16 14  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0047745

> <DATABASE_NAME>
MIME

> <SMILES>
CCCCCC(=O)OCCC1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C14H20O2/c1-2-3-5-10-14(15)16-12-11-13-8-6-4-7-9-13/h4,6-9H,2-3,5,10-12H2,1H3

> <INCHI_KEY>
BUYNWUMUDHPPDS-UHFFFAOYSA-N

> <FORMULA>
C14H20O2

> <MOLECULAR_WEIGHT>
220.3074

> <EXACT_MASS>
220.146329884

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_AVERAGE_POLARIZABILITY>
26.253494379747764

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-phenylethyl hexanoate

> <ALOGPS_LOGP>
4.44

> <JCHEM_LOGP>
3.9699245060000004

> <ALOGPS_LOGS>
-4.48

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-7.033445377011904

> <JCHEM_POLAR_SURFACE_AREA>
26.3

> <JCHEM_REFRACTIVITY>
65.2103

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.25e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-phenylethyl hexanoate

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0037718
     RDKit          3D
2-Phenylethyl hexanoate
 36 36  0  0  0  0  0  0  0  0999 V2000
   -5.0708    0.9644   -0.2521 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3948   -0.3542    0.3374 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5705   -1.4875   -0.1059 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1387   -1.5110    0.2005 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3279   -0.3826   -0.3515 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8815   -0.6097    0.0055 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5749   -1.6212    0.6581 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1157    0.2717   -0.3700 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4602    0.0067   -0.0058 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2969    1.1557   -0.5660 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7095    0.8864   -0.1888 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4967    0.1396   -1.0688 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8111   -0.1584   -0.8044 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3892    0.2858    0.3626 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6096    1.0254    1.2339 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2846    1.3305    0.9761 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4887    0.8547   -1.1695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0270    1.4840   -0.6111 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6131    1.6521    0.4765 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5030   -0.5553    0.1718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2926   -0.2409    1.4652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0566   -2.4258    0.3081 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6902   -1.6162   -1.2238 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6997   -2.4573   -0.2288 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9759   -1.6124    1.3166 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6356    0.5658    0.1469 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4478   -0.3532   -1.4432 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5971   -0.0145    1.0989 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8483   -0.9165   -0.4360 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1828    1.1206   -1.6598 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9862    2.1297   -0.1257 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0406   -0.2078   -1.9840 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4220   -0.7344   -1.4808 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4039    0.0899    0.6291 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0318    1.3933    2.1658 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7034    1.9028    1.6640 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 11  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  2 20  1  0
  2 21  1  0
  3 22  1  0
  3 23  1  0
  4 24  1  0
  4 25  1  0
  5 26  1  0
  5 27  1  0
  9 28  1  0
  9 29  1  0
 10 30  1  0
 10 31  1  0
 12 32  1  0
 13 33  1  0
 14 34  1  0
 15 35  1  0
 16 36  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       5.335   9.240   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.668   8.470   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.002   9.240   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      20.005   6.930   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.336   8.470   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      20.005   8.470   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      18.672   6.160   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      18.672   9.240   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      17.338   6.930   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.669   9.240   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      16.004   9.240   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      14.671   8.470   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      17.338   8.470   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      12.003   8.470   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      12.003   6.930   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0      13.337   9.240   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    5                                                       
CONECT    4    6    7                                                       
CONECT    5    3   10                                                       
CONECT    6    4    8                                                       
CONECT    7    4    9                                                       
CONECT    8    6   13                                                       
CONECT    9    7   13                                                       
CONECT   10    5   14                                                       
CONECT   11   12   13                                                       
CONECT   12   11   16                                                       
CONECT   13    8    9   11                                                  
CONECT   14   10   15   16                                                  
CONECT   15   14                                                            
CONECT   16   12   14                                                       
MASTER        0    0    0    0    0    0    0    0   16    0   32    0
END

COMPND    HMDB0037718
HETATM    1  C1  UNL     1      -5.071   0.964  -0.252  1.00  0.00           C  
HETATM    2  C2  UNL     1      -5.395  -0.354   0.337  1.00  0.00           C  
HETATM    3  C3  UNL     1      -4.570  -1.488  -0.106  1.00  0.00           C  
HETATM    4  C4  UNL     1      -3.139  -1.511   0.200  1.00  0.00           C  
HETATM    5  C5  UNL     1      -2.328  -0.383  -0.352  1.00  0.00           C  
HETATM    6  C6  UNL     1      -0.882  -0.610   0.006  1.00  0.00           C  
HETATM    7  O1  UNL     1      -0.575  -1.621   0.658  1.00  0.00           O  
HETATM    8  O2  UNL     1       0.116   0.272  -0.370  1.00  0.00           O  
HETATM    9  C7  UNL     1       1.460   0.007  -0.006  1.00  0.00           C  
HETATM   10  C8  UNL     1       2.297   1.156  -0.566  1.00  0.00           C  
HETATM   11  C9  UNL     1       3.710   0.886  -0.189  1.00  0.00           C  
HETATM   12  C10 UNL     1       4.497   0.140  -1.069  1.00  0.00           C  
HETATM   13  C11 UNL     1       5.811  -0.158  -0.804  1.00  0.00           C  
HETATM   14  C12 UNL     1       6.389   0.286   0.363  1.00  0.00           C  
HETATM   15  C13 UNL     1       5.610   1.025   1.234  1.00  0.00           C  
HETATM   16  C14 UNL     1       4.285   1.330   0.976  1.00  0.00           C  
HETATM   17  H1  UNL     1      -4.489   0.855  -1.170  1.00  0.00           H  
HETATM   18  H2  UNL     1      -6.027   1.484  -0.611  1.00  0.00           H  
HETATM   19  H3  UNL     1      -4.613   1.652   0.476  1.00  0.00           H  
HETATM   20  H4  UNL     1      -6.503  -0.555   0.172  1.00  0.00           H  
HETATM   21  H5  UNL     1      -5.293  -0.241   1.465  1.00  0.00           H  
HETATM   22  H6  UNL     1      -5.057  -2.426   0.308  1.00  0.00           H  
HETATM   23  H7  UNL     1      -4.690  -1.616  -1.224  1.00  0.00           H  
HETATM   24  H8  UNL     1      -2.700  -2.457  -0.229  1.00  0.00           H  
HETATM   25  H9  UNL     1      -2.976  -1.612   1.317  1.00  0.00           H  
HETATM   26  H10 UNL     1      -2.636   0.566   0.147  1.00  0.00           H  
HETATM   27  H11 UNL     1      -2.448  -0.353  -1.443  1.00  0.00           H  
HETATM   28  H12 UNL     1       1.597  -0.014   1.099  1.00  0.00           H  
HETATM   29  H13 UNL     1       1.848  -0.917  -0.436  1.00  0.00           H  
HETATM   30  H14 UNL     1       2.183   1.121  -1.660  1.00  0.00           H  
HETATM   31  H15 UNL     1       1.986   2.130  -0.126  1.00  0.00           H  
HETATM   32  H16 UNL     1       4.041  -0.208  -1.984  1.00  0.00           H  
HETATM   33  H17 UNL     1       6.422  -0.734  -1.481  1.00  0.00           H  
HETATM   34  H18 UNL     1       7.404   0.090   0.629  1.00  0.00           H  
HETATM   35  H19 UNL     1       6.032   1.393   2.166  1.00  0.00           H  
HETATM   36  H20 UNL     1       3.703   1.903   1.664  1.00  0.00           H  
CONECT    1    2   17   18   19
CONECT    2    3   20   21
CONECT    3    4   22   23
CONECT    4    5   24   25
CONECT    5    6   26   27
CONECT    6    7    7    8
CONECT    8    9
CONECT    9   10   28   29
CONECT   10   11   30   31
CONECT   11   12   12   16
CONECT   12   13   32
CONECT   13   14   14   33
CONECT   14   15   34
CONECT   15   16   16   35
CONECT   16   36
END

HMDB0037718
     RDKit          3D
2-Phenylethyl hexanoate
 36 36  0  0  0  0  0  0  0  0999 V2000
   -5.0708    0.9644   -0.2521 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3948   -0.3542    0.3374 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5705   -1.4875   -0.1059 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1387   -1.5110    0.2005 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3279   -0.3826   -0.3515 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8815   -0.6097    0.0055 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5749   -1.6212    0.6581 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1157    0.2717   -0.3700 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4602    0.0067   -0.0058 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2969    1.1557   -0.5660 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7095    0.8864   -0.1888 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4967    0.1396   -1.0688 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8111   -0.1584   -0.8044 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3892    0.2858    0.3626 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6096    1.0254    1.2339 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2846    1.3305    0.9761 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4887    0.8547   -1.1695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0270    1.4840   -0.6111 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6131    1.6521    0.4765 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5030   -0.5553    0.1718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2926   -0.2409    1.4652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0566   -2.4258    0.3081 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6902   -1.6162   -1.2238 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6997   -2.4573   -0.2288 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9759   -1.6124    1.3166 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6356    0.5658    0.1469 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4478   -0.3532   -1.4432 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5971   -0.0145    1.0989 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8483   -0.9165   -0.4360 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1828    1.1206   -1.6598 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9862    2.1297   -0.1257 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0406   -0.2078   -1.9840 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4220   -0.7344   -1.4808 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4039    0.0899    0.6291 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0318    1.3933    2.1658 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7034    1.9028    1.6640 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 11  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  2 20  1  0
  2 21  1  0
  3 22  1  0
  3 23  1  0
  4 24  1  0
  4 25  1  0
  5 26  1  0
  5 27  1  0
  9 28  1  0
  9 29  1  0
 10 30  1  0
 10 31  1  0
 12 32  1  0
 13 33  1  0
 14 34  1  0
 15 35  1  0
 16 36  1  0
M  END

Synonyms

Value	Source
2-Phenylethyl hexanoic acid	Generator
2-Phenethyl hexanoate	HMDB
2-Phenylethyl caproate	HMDB
Benzylcarbinyl caproate	HMDB
Benzylcarbinyl hexanoate	HMDB
FEMA 3221	HMDB
Hexanoic acid, 2-phenylethyl ester	HMDB
Hexanoic acid, phenethyl ester	HMDB
Phenethyl caproate	HMDB
Phenethyl hexanoate	HMDB
Phenylethyl caproate	HMDB
Phenylethyl hexanoate	HMDB
Phenylethyl N-hexanoate	HMDB

Molecular Formula

C₁₄H₂₀O₂

Average Mass

220.3074

Monoisotopic Mass

220.146329884

IUPAC Name

2-phenylethyl hexanoate

Traditional Name

2-phenylethyl hexanoate

CAS Registry Number

Not Available

SMILES

CCCCCC(=O)OCCC1=CC=CC=C1

InChI Identifier

InChI=1S/C14H20O2/c1-2-3-5-10-14(15)16-12-11-13-8-6-4-7-9-13/h4,6-9H,2-3,5,10-12H2,1H3

InChI Key

BUYNWUMUDHPPDS-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as fatty acid esters. These are carboxylic ester derivatives of a fatty acid.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acid esters

Direct Parent

Fatty acid esters

Alternative Parents

Substituents

Fatty acid ester
Benzenoid
Monocyclic benzene moiety
Carboxylic acid ester
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Not Available

Predicted Properties

Property	Value	Source
Water Solubility	0.0072 g/L	ALOGPS
logP	4.44	ALOGPS
logP	3.97	ChemAxon
logS	-4.5	ALOGPS
pKa (Strongest Basic)	-7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	26.3 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	65.21 m³·mol⁻¹	ChemAxon
Polarizability	26.25 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Spectrum Type	Description	Splash Key	Deposition Date	View
GC-MS	GC-MS Spectrum - EI-B (Non-derivatized)	splash10-0udi-4900000000-0841c992786af8b784b3	2017-09-12	View Spectrum
GC-MS	GC-MS Spectrum - EI-B (Non-derivatized)	splash10-0udi-4900000000-0841c992786af8b784b3	2018-05-18	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positive	splash10-0006-9300000000-71553d18952542a9e7a6	2016-09-22	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
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	splash10-00di-6590000000-76ec7840a91d240721e1	2016-08-01	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-0a4i-9810000000-45ac60b4ec807dd6b457	2016-08-01	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-0a4l-9200000000-516bf27053410f8c88b4	2016-08-01	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	splash10-014j-7490000000-734c57e5cd66038634d2	2016-08-03	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	splash10-014j-9810000000-3602f438a99d35ef24f4	2016-08-03	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	splash10-0007-9100000000-5499d339db07ef85a615	2016-08-03	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	splash10-0002-9100000000-fb53d9de9fb85f36326e	2021-09-22	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	splash10-002g-9200000000-1d68dca13f7655194ad0	2021-09-22	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	splash10-0a4m-9000000000-d1edd252e08f751d44b5	2021-09-22	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	splash10-0a4i-6910000000-40664de3608c721fce38	2021-09-22	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-0a4i-5900000000-7b6634edc631b225fcdf	2021-09-22	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-052f-9400000000-38eea0cdbc030c734d97	2021-09-22	View Spectrum

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	Ascomycota	1	Human feces; Human saliva	Unknown

Exposure Sources

Other Exposures

Source Type	Activity	Data Source	Reference
Cosmetics	Not Available	U.S. Environmental Protection Agency	CompTox
Domestics	Not Available	U.S. Environmental Protection Agency	CompTox
Domestics	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

External Links

HMDB ID

HMDB0037718

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB016847

KNApSAcK ID

Not Available

Chemspider ID

55313

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

61384

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

General References

Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. doi: 10.1038/35036052. [PubMed:11413487 ]
Watson AD: Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Lipidomics: a global approach to lipid analysis in biological systems. J Lipid Res. 2006 Oct;47(10):2101-11. doi: 10.1194/jlr.R600022-JLR200. Epub 2006 Aug 10. [PubMed:16902246 ]
Sethi JK, Vidal-Puig AJ: Thematic review series: adipocyte biology. Adipose tissue function and plasticity orchestrate nutritional adaptation. J Lipid Res. 2007 Jun;48(6):1253-62. doi: 10.1194/jlr.R700005-JLR200. Epub 2007 Mar 20. [PubMed:17374880 ]
Lingwood D, Simons K: Lipid rafts as a membrane-organizing principle. Science. 2010 Jan 1;327(5961):46-50. doi: 10.1126/science.1174621. [PubMed:20044567 ]
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..
Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.

Showing metabocard for Phenethyl hexanoate (MMDBc0047745)

MOL for #<Metabolite:0x00007fca68d9f7a8>

3D MOL for #<Metabolite:0x00007fca68d9f7a8>

3D SDF for #<Metabolite:0x00007fca68d9f7a8>

3D-SDF for #<Metabolite:0x00007fca68d9f7a8>

PDB for #<Metabolite:0x00007fca68d9f7a8>

3D PDB for #<Metabolite:0x00007fca68d9f7a8>

SMILES for #<Metabolite:0x00007fca68d9f7a8>

INCHI for #<Metabolite:0x00007fca68d9f7a8>

Structure for #<Metabolite:0x00007fca68d9f7a8>

3D Structure for #<Metabolite:0x00007fca68d9f7a8>