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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 17:40:12 UTC

Update Date

2022-03-07 02:52:46 UTC

HMDB ID

HMDB0030983

Secondary Accession Numbers

HMDB30983

Metabolite Identification

Common Name

5-(8-Pentadecenyl)-1,3-benzenediol

Description

5-(8-Pentadecenyl)-1,3-benzenediol, also known as bilobol, belongs to the class of organic compounds known as resorcinols. Resorcinols are compounds containing a resorcinol moiety, which is a benzene ring bearing two hydroxyl groups at positions 1 and 3. 5-(8-Pentadecenyl)-1,3-benzenediol has been detected, but not quantified in, a few different foods, such as cashew nuts (Anacardium occidentale), fats and oils, and ginkgo nuts (Ginkgo biloba). This could make 5-(8-pentadecenyl)-1,3-benzenediol a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on 5-(8-Pentadecenyl)-1,3-benzenediol.

Structure

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

HMDB0030983
     RDKit          3D
5-(8-Pentadecenyl)-1,3-benzenediol
 57 57  0  0  0  0  0  0  0  0999 V2000
    8.0872    2.4070    0.7301 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2103    1.2380    0.3123 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9179    1.3670   -1.1658 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0590    0.2688   -1.6989 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7235    0.2514   -0.9834 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8372   -0.8635   -1.5177 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5506   -0.7909   -0.7468 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0989   -1.7764   -0.0141 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8184   -1.6678    0.7363 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1891   -0.3289    0.5139 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1123   -0.1836    1.2660 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1393   -1.2096    0.8589 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3883   -0.9733    1.6651 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5038   -1.9087    1.3585 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0129   -1.8241   -0.0585 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5735   -0.4994   -0.3734 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9244   -0.2884   -0.0968 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5377    0.9155   -0.3631 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8801    1.1623   -0.1014 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8069    1.9575   -0.9215 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4697    1.7631   -1.2005 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7536    2.8127   -1.7578 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8647    0.5271   -0.9208 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5576    3.1203    1.3822 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4372    2.9616   -0.1617 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9469    1.9910    1.3219 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3005    1.2991    0.9401 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7178    0.2729    0.5147 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8943    1.3632   -1.6906 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3742    2.3315   -1.3275 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9630    0.3827   -2.7770 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5586   -0.7035   -1.4790 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1772    1.2005   -1.1497 H   0  0  0  0  0  0  0  0  0  0  0  0
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    3.5667   -0.6033   -2.5729 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3096   -1.8497   -1.4417 H   0  0  0  0  0  0  0  0  0  0  0  0
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    2.6944   -2.6892    0.0312 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1607   -2.5061    0.4261 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.8295    0.4160   -1.1556 H   0  0  0  0  0  0  0  0  0  0  0  0
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 23 57  1  0
M  END


  Mrv0541 05061305382D          

 23 23  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
   -2.1434   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    7.8592   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    9.2881   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -7.4250    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
  4  3  1  0  0  0  0
  5  4  1  0  0  0  0
  6  5  1  0  0  0  0
  7  6  1  0  0  0  0
  8  7  2  0  0  0  0
  9  8  1  0  0  0  0
 10  9  1  0  0  0  0
 11 10  1  0  0  0  0
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 13 12  1  0  0  0  0
 14 13  1  0  0  0  0
 15 14  1  0  0  0  0
 19 15  1  0  0  0  0
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 21 17  2  0  0  0  0
 21 18  1  0  0  0  0
 22 20  1  0  0  0  0
 23 21  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0030983

> <DATABASE_NAME>
hmdb

> <SMILES>
CCCCCC\C=C\CCCCCCCC1=CC(O)=CC(O)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C21H34O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-19-16-20(22)18-21(23)17-19/h7-8,16-18,22-23H,2-6,9-15H2,1H3/b8-7+

> <INCHI_KEY>
TUGAUFMQYWZJAB-BQYQJAHWSA-N

> <FORMULA>
C21H34O2

> <MOLECULAR_WEIGHT>
318.4935

> <EXACT_MASS>
318.255880332

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_AVERAGE_POLARIZABILITY>
41.23941214184833

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
5-[(8E)-pentadec-8-en-1-yl]benzene-1,3-diol

> <ALOGPS_LOGP>
8.00

> <JCHEM_LOGP>
7.741576215333334

> <ALOGPS_LOGS>
-5.98

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.811350807001979

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.359032641616453

> <JCHEM_PKA_STRONGEST_BASIC>
-5.665057916048885

> <JCHEM_POLAR_SURFACE_AREA>
40.46

> <JCHEM_REFRACTIVITY>
100.59159999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.32e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-[(8E)-pentadec-8-en-1-yl]benzene-1,3-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0030983
     RDKit          3D
5-(8-Pentadecenyl)-1,3-benzenediol
 57 57  0  0  0  0  0  0  0  0999 V2000
    8.0872    2.4070    0.7301 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2103    1.2380    0.3123 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9179    1.3670   -1.1658 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0590    0.2688   -1.6989 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7235    0.2514   -0.9834 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8372   -0.8635   -1.5177 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5506   -0.7909   -0.7468 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0989   -1.7764   -0.0141 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8184   -1.6678    0.7363 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1891   -0.3289    0.5139 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1123   -0.1836    1.2660 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1393   -1.2096    0.8589 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.0129   -1.8241   -0.0585 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5735   -0.4994   -0.3734 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.5377    0.9155   -0.3631 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8801    1.1623   -0.1014 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8069    1.9575   -0.9215 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4697    1.7631   -1.2005 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7536    2.8127   -1.7578 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8647    0.5271   -0.9208 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5576    3.1203    1.3822 H   0  0  0  0  0  0  0  0  0  0  0  0
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    8.9469    1.9910    1.3219 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3005    1.2991    0.9401 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7178    0.2729    0.5147 H   0  0  0  0  0  0  0  0  0  0  0  0
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    4.1772    1.2005   -1.1497 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.1282   -1.1101    2.7462 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.2703   -2.9683    1.6324 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.1864   -2.0008   -0.7812 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5369   -1.0801    0.3424 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4489    0.4081    0.3131 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2770    2.9133   -1.1373 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7806    2.7588   -1.9918 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8295    0.4160   -1.1556 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  1  0
  7  8  2  0
  8  9  1  0
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 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  1  0
 18 20  2  0
 20 21  1  0
 21 22  1  0
 21 23  2  0
 23 16  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  2 27  1  0
  2 28  1  0
  3 29  1  0
  3 30  1  0
  4 31  1  0
  4 32  1  0
  5 33  1  0
  5 34  1  0
  6 35  1  0
  6 36  1  0
  7 37  1  0
  8 38  1  0
  9 39  1  0
  9 40  1  0
 10 41  1  0
 10 42  1  0
 11 43  1  0
 11 44  1  0
 12 45  1  0
 12 46  1  0
 13 47  1  0
 13 48  1  0
 14 49  1  0
 14 50  1  0
 15 51  1  0
 15 52  1  0
 17 53  1  0
 19 54  1  0
 20 55  1  0
 22 56  1  0
 23 57  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      -4.001 -10.010   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.667  -9.240   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.334 -10.010   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.000  -9.240   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.334 -10.010   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.667  -9.240   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.001 -10.010   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.335  -9.240   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.668 -10.010   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.002  -9.240   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.336 -10.010   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.669  -9.240   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      12.003 -10.010   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      13.337  -9.240   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      16.004  -9.240   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      14.671 -11.550   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      17.338 -11.550   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      14.671 -10.010   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      17.338 -10.010   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      16.004 -12.320   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      18.672  -9.240   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      16.004 -13.860   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   19                                                       
CONECT   16   19   20                                                       
CONECT   17   19   21                                                       
CONECT   18   20   21                                                       
CONECT   19   15   16   17                                                  
CONECT   20   16   18   22                                                  
CONECT   21   17   18   23                                                  
CONECT   22   20                                                            
CONECT   23   21                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   46    0
END

COMPND    HMDB0030983
HETATM    1  C1  UNL     1       8.087   2.407   0.730  1.00  0.00           C  
HETATM    2  C2  UNL     1       7.210   1.238   0.312  1.00  0.00           C  
HETATM    3  C3  UNL     1       6.918   1.367  -1.166  1.00  0.00           C  
HETATM    4  C4  UNL     1       6.059   0.269  -1.699  1.00  0.00           C  
HETATM    5  C5  UNL     1       4.724   0.251  -0.983  1.00  0.00           C  
HETATM    6  C6  UNL     1       3.837  -0.864  -1.518  1.00  0.00           C  
HETATM    7  C7  UNL     1       2.551  -0.791  -0.747  1.00  0.00           C  
HETATM    8  C8  UNL     1       2.099  -1.776  -0.014  1.00  0.00           C  
HETATM    9  C9  UNL     1       0.818  -1.668   0.736  1.00  0.00           C  
HETATM   10  C10 UNL     1       0.189  -0.329   0.514  1.00  0.00           C  
HETATM   11  C11 UNL     1      -1.112  -0.184   1.266  1.00  0.00           C  
HETATM   12  C12 UNL     1      -2.139  -1.210   0.859  1.00  0.00           C  
HETATM   13  C13 UNL     1      -3.388  -0.973   1.665  1.00  0.00           C  
HETATM   14  C14 UNL     1      -4.504  -1.909   1.358  1.00  0.00           C  
HETATM   15  C15 UNL     1      -5.013  -1.824  -0.059  1.00  0.00           C  
HETATM   16  C16 UNL     1      -5.573  -0.499  -0.373  1.00  0.00           C  
HETATM   17  C17 UNL     1      -6.924  -0.288  -0.097  1.00  0.00           C  
HETATM   18  C18 UNL     1      -7.538   0.916  -0.363  1.00  0.00           C  
HETATM   19  O1  UNL     1      -8.880   1.162  -0.101  1.00  0.00           O  
HETATM   20  C19 UNL     1      -6.807   1.958  -0.922  1.00  0.00           C  
HETATM   21  C20 UNL     1      -5.470   1.763  -1.201  1.00  0.00           C  
HETATM   22  O2  UNL     1      -4.754   2.813  -1.758  1.00  0.00           O  
HETATM   23  C21 UNL     1      -4.865   0.527  -0.921  1.00  0.00           C  
HETATM   24  H1  UNL     1       7.558   3.120   1.382  1.00  0.00           H  
HETATM   25  H2  UNL     1       8.437   2.962  -0.162  1.00  0.00           H  
HETATM   26  H3  UNL     1       8.947   1.991   1.322  1.00  0.00           H  
HETATM   27  H4  UNL     1       6.301   1.299   0.940  1.00  0.00           H  
HETATM   28  H5  UNL     1       7.718   0.273   0.515  1.00  0.00           H  
HETATM   29  H6  UNL     1       7.894   1.363  -1.691  1.00  0.00           H  
HETATM   30  H7  UNL     1       6.374   2.332  -1.328  1.00  0.00           H  
HETATM   31  H8  UNL     1       5.963   0.383  -2.777  1.00  0.00           H  
HETATM   32  H9  UNL     1       6.559  -0.704  -1.479  1.00  0.00           H  
HETATM   33  H10 UNL     1       4.177   1.200  -1.150  1.00  0.00           H  
HETATM   34  H11 UNL     1       4.870   0.113   0.104  1.00  0.00           H  
HETATM   35  H12 UNL     1       3.567  -0.603  -2.573  1.00  0.00           H  
HETATM   36  H13 UNL     1       4.310  -1.850  -1.442  1.00  0.00           H  
HETATM   37  H14 UNL     1       2.002   0.134  -0.826  1.00  0.00           H  
HETATM   38  H15 UNL     1       2.694  -2.689   0.031  1.00  0.00           H  
HETATM   39  H16 UNL     1       0.161  -2.506   0.426  1.00  0.00           H  
HETATM   40  H17 UNL     1       0.996  -1.759   1.847  1.00  0.00           H  
HETATM   41  H18 UNL     1       0.015  -0.215  -0.596  1.00  0.00           H  
HETATM   42  H19 UNL     1       0.878   0.448   0.897  1.00  0.00           H  
HETATM   43  H20 UNL     1      -0.881  -0.241   2.345  1.00  0.00           H  
HETATM   44  H21 UNL     1      -1.514   0.816   1.063  1.00  0.00           H  
HETATM   45  H22 UNL     1      -1.772  -2.249   1.021  1.00  0.00           H  
HETATM   46  H23 UNL     1      -2.385  -1.145  -0.210  1.00  0.00           H  
HETATM   47  H24 UNL     1      -3.768   0.066   1.548  1.00  0.00           H  
HETATM   48  H25 UNL     1      -3.128  -1.110   2.746  1.00  0.00           H  
HETATM   49  H26 UNL     1      -5.348  -1.631   2.049  1.00  0.00           H  
HETATM   50  H27 UNL     1      -4.270  -2.968   1.632  1.00  0.00           H  
HETATM   51  H28 UNL     1      -5.818  -2.600  -0.208  1.00  0.00           H  
HETATM   52  H29 UNL     1      -4.186  -2.001  -0.781  1.00  0.00           H  
HETATM   53  H30 UNL     1      -7.537  -1.080   0.342  1.00  0.00           H  
HETATM   54  H31 UNL     1      -9.449   0.408   0.313  1.00  0.00           H  
HETATM   55  H32 UNL     1      -7.277   2.913  -1.137  1.00  0.00           H  
HETATM   56  H33 UNL     1      -3.781   2.759  -1.992  1.00  0.00           H  
HETATM   57  H34 UNL     1      -3.829   0.416  -1.156  1.00  0.00           H  
CONECT    1    2   24   25   26
CONECT    2    3   27   28
CONECT    3    4   29   30
CONECT    4    5   31   32
CONECT    5    6   33   34
CONECT    6    7   35   36
CONECT    7    8    8   37
CONECT    8    9   38
CONECT    9   10   39   40
CONECT   10   11   41   42
CONECT   11   12   43   44
CONECT   12   13   45   46
CONECT   13   14   47   48
CONECT   14   15   49   50
CONECT   15   16   51   52
CONECT   16   17   17   23
CONECT   17   18   53
CONECT   18   19   20   20
CONECT   19   54
CONECT   20   21   55
CONECT   21   22   23   23
CONECT   22   56
CONECT   23   57
END

HMDB0030983
     RDKit          3D
5-(8-Pentadecenyl)-1,3-benzenediol
 57 57  0  0  0  0  0  0  0  0999 V2000
    8.0872    2.4070    0.7301 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2103    1.2380    0.3123 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9179    1.3670   -1.1658 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0590    0.2688   -1.6989 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7235    0.2514   -0.9834 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8372   -0.8635   -1.5177 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5506   -0.7909   -0.7468 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0989   -1.7764   -0.0141 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8184   -1.6678    0.7363 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1891   -0.3289    0.5139 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1123   -0.1836    1.2660 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1393   -1.2096    0.8589 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3883   -0.9733    1.6651 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5038   -1.9087    1.3585 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0129   -1.8241   -0.0585 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5735   -0.4994   -0.3734 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9244   -0.2884   -0.0968 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5377    0.9155   -0.3631 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8801    1.1623   -0.1014 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8069    1.9575   -0.9215 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4697    1.7631   -1.2005 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7536    2.8127   -1.7578 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8647    0.5271   -0.9208 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5576    3.1203    1.3822 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4372    2.9616   -0.1617 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9469    1.9910    1.3219 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3005    1.2991    0.9401 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7178    0.2729    0.5147 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8943    1.3632   -1.6906 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3742    2.3315   -1.3275 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9630    0.3827   -2.7770 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5586   -0.7035   -1.4790 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1772    1.2005   -1.1497 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8703    0.1126    0.1041 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5667   -0.6033   -2.5729 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3096   -1.8497   -1.4417 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0017    0.1344   -0.8257 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6944   -2.6892    0.0312 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1607   -2.5061    0.4261 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9958   -1.7588    1.8472 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0146   -0.2153   -0.5957 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8776    0.4484    0.8966 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8810   -0.2410    2.3452 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5140    0.8157    1.0632 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7719   -2.2495    1.0212 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3845   -1.1453   -0.2102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7683    0.0661    1.5480 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1282   -1.1101    2.7462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3483   -1.6306    2.0489 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2703   -2.9683    1.6324 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8176   -2.6004   -0.2079 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1864   -2.0008   -0.7812 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5369   -1.0801    0.3424 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4489    0.4081    0.3131 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2770    2.9133   -1.1373 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7806    2.7588   -1.9918 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8295    0.4160   -1.1556 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  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  1  0
 18 20  2  0
 20 21  1  0
 21 22  1  0
 21 23  2  0
 23 16  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  2 27  1  0
  2 28  1  0
  3 29  1  0
  3 30  1  0
  4 31  1  0
  4 32  1  0
  5 33  1  0
  5 34  1  0
  6 35  1  0
  6 36  1  0
  7 37  1  0
  8 38  1  0
  9 39  1  0
  9 40  1  0
 10 41  1  0
 10 42  1  0
 11 43  1  0
 11 44  1  0
 12 45  1  0
 12 46  1  0
 13 47  1  0
 13 48  1  0
 14 49  1  0
 14 50  1  0
 15 51  1  0
 15 52  1  0
 17 53  1  0
 19 54  1  0
 20 55  1  0
 22 56  1  0
 23 57  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
Bilobol	MeSH
5-[(8Z)-Pentadec-8-en-1-yl]benzene-1,3-diol	HMDB
5-[(8Z)-Pentadec-8-enyl]resorcinol	HMDB
Cardolmonoene	HMDB
Trifurcatol a2	HMDB
5-(8-Pentadecenyl)-1,3-benzenediol	MeSH

Chemical Formula

C₂₁H₃₄O₂

Average Molecular Weight

318.4935

Monoisotopic Molecular Weight

318.255880332

IUPAC Name

5-[(8E)-pentadec-8-en-1-yl]benzene-1,3-diol

Traditional Name

5-[(8E)-pentadec-8-en-1-yl]benzene-1,3-diol

CAS Registry Number

22910-86-7

SMILES

CCCCCC\C=C\CCCCCCCC1=CC(O)=CC(O)=C1

InChI Identifier

InChI=1S/C21H34O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-19-16-20(22)18-21(23)17-19/h7-8,16-18,22-23H,2-6,9-15H2,1H3/b8-7+

InChI Key

TUGAUFMQYWZJAB-BQYQJAHWSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as resorcinols. Resorcinols are compounds containing a resorcinol moiety, which is a benzene ring bearing two hydroxyl groups at positions 1 and 3.

Kingdom

Super Class

Class

Sub Class

Direct Parent

Alternative Parents

Substituents

Resorcinol
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Monocyclic benzene moiety
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cell membrane (HMDB: HMDB0030983)

Cellular substructure

Membrane (HMDB: HMDB0030983)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0030983)

Source

Endogenous

Endogenous (HMDB: HMDB0030983)

Plant

Plant (HMDB: HMDB0030983)

Exogenous

Food

Food (HMDB: HMDB0030983)

Nut

Cashew nut (FooDB: FOOD00011)

Herb and spice

Other seed

Ginkgo nuts (FooDB: FOOD00367)

Fat and oil

Fats and oils (FooDB: FOOD00864)

Process

Not Available

Role

Not Available

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	36 - 37 °C	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	0.0033 mg/L @ 25 °C (est)	The Good Scents Company Information System
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.00033 g/L	ALOGPS
logP	8	ALOGPS
logP	7.74	ChemAxon
logS	-6	ALOGPS
pKa (Strongest Acidic)	9.36	ChemAxon
pKa (Strongest Basic)	-5.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	40.46 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	100.59 m³·mol⁻¹	ChemAxon
Polarizability	41.24 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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
DarkChem	[M+H]+	184.356	31661259
DarkChem	[M-H]-	189.587	31661259
DeepCCS	[M+H]+	192.81	30932474
DeepCCS	[M-H]-	190.452	30932474
DeepCCS	[M-2H]-	223.338	30932474
DeepCCS	[M+Na]+	198.975	30932474
AllCCS	[M+H]+	187.3	32859911
AllCCS	[M+H-H2O]+	184.4	32859911
AllCCS	[M+NH4]+	190.0	32859911
AllCCS	[M+Na]+	190.8	32859911
AllCCS	[M-H]-	189.0	32859911
AllCCS	[M+Na-2H]-	190.6	32859911
AllCCS	[M+HCOO]-	192.5	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
5-(8-Pentadecenyl)-1,3-benzenediol	CCCCCC\C=C\CCCCCCCC1=CC(O)=CC(O)=C1	3560.1	Standard polar	33892256
5-(8-Pentadecenyl)-1,3-benzenediol	CCCCCC\C=C\CCCCCCCC1=CC(O)=CC(O)=C1	2713.1	Standard non polar	33892256
5-(8-Pentadecenyl)-1,3-benzenediol	CCCCCC\C=C\CCCCCCCC1=CC(O)=CC(O)=C1	2807.1	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
5-(8-Pentadecenyl)-1,3-benzenediol,1TMS,isomer #1	CCCCCC/C=C/CCCCCCCC1=CC(O)=CC(O[Si](C)(C)C)=C1	2750.9	Semi standard non polar	33892256
5-(8-Pentadecenyl)-1,3-benzenediol,2TMS,isomer #1	CCCCCC/C=C/CCCCCCCC1=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1	2673.8	Semi standard non polar	33892256
5-(8-Pentadecenyl)-1,3-benzenediol,1TBDMS,isomer #1	CCCCCC/C=C/CCCCCCCC1=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C1	2987.1	Semi standard non polar	33892256
5-(8-Pentadecenyl)-1,3-benzenediol,2TBDMS,isomer #1	CCCCCC/C=C/CCCCCCCC1=CC(O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C1	3116.3	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 - 5-(8-Pentadecenyl)-1,3-benzenediol GC-MS (Non-derivatized) - 70eV, Positive	splash10-00di-4920000000-4d86731d18b3b6767828	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 5-(8-Pentadecenyl)-1,3-benzenediol GC-MS (2 TMS) - 70eV, Positive	splash10-006w-8923400000-31116db0448e0ef5f62d	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 5-(8-Pentadecenyl)-1,3-benzenediol 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 - 5-(8-Pentadecenyl)-1,3-benzenediol 10V, Positive-QTOF	splash10-014i-0119000000-edc71902749cb9b3b35c	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-(8-Pentadecenyl)-1,3-benzenediol 20V, Positive-QTOF	splash10-014j-6963000000-4a238b90a5b11b7e3763	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-(8-Pentadecenyl)-1,3-benzenediol 40V, Positive-QTOF	splash10-0006-9840000000-4c2bedb7468378830d6b	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-(8-Pentadecenyl)-1,3-benzenediol 10V, Negative-QTOF	splash10-014i-0009000000-60c6e04f3a600b792649	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-(8-Pentadecenyl)-1,3-benzenediol 20V, Negative-QTOF	splash10-014i-0019000000-e5f900256785603f3d96	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-(8-Pentadecenyl)-1,3-benzenediol 40V, Negative-QTOF	splash10-0ftf-2792000000-8371181e4026377c0b94	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-(8-Pentadecenyl)-1,3-benzenediol 10V, Positive-QTOF	splash10-014i-1019000000-08c13c52e27ee70d99b1	2021-09-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-(8-Pentadecenyl)-1,3-benzenediol 20V, Positive-QTOF	splash10-014i-9717000000-3a469f8c69425ef2a756	2021-09-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-(8-Pentadecenyl)-1,3-benzenediol 40V, Positive-QTOF	splash10-00mo-9200000000-82a148adf2687f78d049	2021-09-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-(8-Pentadecenyl)-1,3-benzenediol 10V, Negative-QTOF	splash10-014i-0009000000-bbaa566ea695ae62f84e	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-(8-Pentadecenyl)-1,3-benzenediol 20V, Negative-QTOF	splash10-014i-0009000000-7966f1d4a8d5c59d3191	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-(8-Pentadecenyl)-1,3-benzenediol 40V, Negative-QTOF	splash10-00dr-3910000000-5bc2cbd2381efc397155	2021-09-25	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

FDB002971

KNApSAcK ID

C00002640

Chemspider ID

5291955

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

6916254

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

rw1824091

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 5-(8-Pentadecenyl)-1,3-benzenediol (HMDB0030983)

MOL for HMDB0030983 (5-(8-Pentadecenyl)-1,3-benzenediol)

3D MOL for HMDB0030983 (5-(8-Pentadecenyl)-1,3-benzenediol)

3D SDF for HMDB0030983 (5-(8-Pentadecenyl)-1,3-benzenediol)

3D-SDF for HMDB0030983 (5-(8-Pentadecenyl)-1,3-benzenediol)

PDB for HMDB0030983 (5-(8-Pentadecenyl)-1,3-benzenediol)

3D PDB for HMDB0030983 (5-(8-Pentadecenyl)-1,3-benzenediol)

SMILES for HMDB0030983 (5-(8-Pentadecenyl)-1,3-benzenediol)

INCHI for HMDB0030983 (5-(8-Pentadecenyl)-1,3-benzenediol)

Structure for HMDB0030983 (5-(8-Pentadecenyl)-1,3-benzenediol)

3D Structure for HMDB0030983 (5-(8-Pentadecenyl)-1,3-benzenediol)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra