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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 23:24:09 UTC

Update Date

2022-03-07 02:55:38 UTC

HMDB ID

HMDB0038118

Secondary Accession Numbers

HMDB38118

Metabolite Identification

Common Name

gamma-Selinene

Description

gamma-Selinene, also known as γ-selinene, belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. Based on a literature review a significant number of articles have been published on gamma-Selinene.

Structure

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

HMDB0038118
     RDKit          3D
gamma-Selinene
 39 40  0  0  0  0  0  0  0  0999 V2000
   -1.4734    2.7582    0.5713 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7363    1.4798    0.3715 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1028    1.0079    0.6914 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3733   -0.3926    0.2803 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4625   -0.8687   -0.8393 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0530   -0.8211   -0.2955 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0204   -1.5545    1.0267 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0587   -1.4810   -1.2065 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1779   -0.6812   -1.4501 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6666    0.0412   -0.2477 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9458    0.1044    0.0783 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9952   -0.5464   -0.7391 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3553    0.8455    1.2984 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6359    0.7144    0.6051 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6623    0.6249   -0.1505 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2505    3.3963    0.9528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4982    3.2021    0.3662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2449    1.0871    1.7908 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8526    1.6756    0.1856 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2513   -1.0734    1.1493 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4100   -0.4791   -0.0978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7681   -1.8705   -1.1606 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5005   -0.1224   -1.6730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0229   -1.9994    1.2418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7273   -2.4118    0.9249 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3438   -0.9261    1.8766 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5326   -1.6875   -2.1867 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2535   -2.4911   -0.8160 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9930   -1.4069   -1.7415 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0786   -0.0106   -2.3297 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0306   -1.6207   -0.4029 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7942   -0.4644   -1.8285 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9722   -0.0823   -0.4975 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5789    0.8438    2.0880 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5660    1.9025    0.9900 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2566    0.3744    1.7558 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5996    0.1741    1.5763 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8836    1.7687    0.7947 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4381    0.9908   -1.1952 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  3
 11 12  1  0
 11 13  1  0
 10 14  1  0
 14 15  1  0
 15  2  1  0
 15  6  1  0
  1 16  1  0
  1 17  1  0
  3 18  1  0
  3 19  1  0
  4 20  1  0
  4 21  1  0
  5 22  1  0
  5 23  1  0
  7 24  1  0
  7 25  1  0
  7 26  1  0
  8 27  1  0
  8 28  1  0
  9 29  1  0
  9 30  1  0
 12 31  1  0
 12 32  1  0
 12 33  1  0
 13 34  1  0
 13 35  1  0
 13 36  1  0
 14 37  1  0
 14 38  1  0
 15 39  1  0
M  END


  Mrv0541 05061310142D          

 15 16  0  0  0  0            999 V2000
    5.7158    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  1  0  0  0  0
  8  5  1  0  0  0  0
  9  7  1  0  0  0  0
 11  1  1  0  0  0  0
 11  2  1  0  0  0  0
 12  3  2  0  0  0  0
 12  6  1  0  0  0  0
 13  7  1  0  0  0  0
 13 10  1  0  0  0  0
 13 11  2  0  0  0  0
 14 10  1  0  0  0  0
 14 12  1  0  0  0  0
 15  4  1  0  0  0  0
 15  8  1  0  0  0  0
 15  9  1  0  0  0  0
 15 14  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0038118

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(C)=C1CCC2(C)CCCC(=C)C2C1

> <INCHI_IDENTIFIER>
InChI=1S/C15H24/c1-11(2)13-7-9-15(4)8-5-6-12(3)14(15)10-13/h14H,3,5-10H2,1-2,4H3

> <INCHI_KEY>
RMZHSBMIZBMVMN-UHFFFAOYSA-N

> <FORMULA>
C15H24

> <MOLECULAR_WEIGHT>
204.3511

> <EXACT_MASS>
204.187800768

> <JCHEM_ACCEPTOR_COUNT>
0

> <JCHEM_AVERAGE_POLARIZABILITY>
26.149891349693185

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4a-methyl-1-methylidene-7-(propan-2-ylidene)-decahydronaphthalene

> <ALOGPS_LOGP>
5.27

> <JCHEM_LOGP>
4.475651567

> <ALOGPS_LOGS>
-4.09

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_POLAR_SURFACE_AREA>
0

> <JCHEM_REFRACTIVITY>
67.1858

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.66e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4a-methyl-1-methylidene-7-(propan-2-ylidene)-hexahydro-2H-naphthalene

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0038118
     RDKit          3D
gamma-Selinene
 39 40  0  0  0  0  0  0  0  0999 V2000
   -1.4734    2.7582    0.5713 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7363    1.4798    0.3715 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1028    1.0079    0.6914 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3733   -0.3926    0.2803 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4625   -0.8687   -0.8393 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0530   -0.8211   -0.2955 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0204   -1.5545    1.0267 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0587   -1.4810   -1.2065 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1779   -0.6812   -1.4501 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6666    0.0412   -0.2477 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9458    0.1044    0.0783 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9952   -0.5464   -0.7391 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3553    0.8455    1.2984 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6359    0.7144    0.6051 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6623    0.6249   -0.1505 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2505    3.3963    0.9528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4982    3.2021    0.3662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2449    1.0871    1.7908 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8526    1.6756    0.1856 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2513   -1.0734    1.1493 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4100   -0.4791   -0.0978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7681   -1.8705   -1.1606 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5005   -0.1224   -1.6730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0229   -1.9994    1.2418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7273   -2.4118    0.9249 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3438   -0.9261    1.8766 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5326   -1.6875   -2.1867 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2535   -2.4911   -0.8160 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9930   -1.4069   -1.7415 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0786   -0.0106   -2.3297 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0306   -1.6207   -0.4029 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7942   -0.4644   -1.8285 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9722   -0.0823   -0.4975 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5789    0.8438    2.0880 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5660    1.9025    0.9900 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2566    0.3744    1.7558 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5996    0.1741    1.5763 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8836    1.7687    0.7947 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4381    0.9908   -1.1952 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  3
 11 12  1  0
 11 13  1  0
 10 14  1  0
 14 15  1  0
 15  2  1  0
 15  6  1  0
  1 16  1  0
  1 17  1  0
  3 18  1  0
  3 19  1  0
  4 20  1  0
  4 21  1  0
  5 22  1  0
  5 23  1  0
  7 24  1  0
  7 25  1  0
  7 26  1  0
  8 27  1  0
  8 28  1  0
  9 29  1  0
  9 30  1  0
 12 31  1  0
 12 32  1  0
 12 33  1  0
 13 34  1  0
 13 35  1  0
 13 36  1  0
 14 37  1  0
 14 38  1  0
 15 39  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      10.669   0.000   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.336  -2.310   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.335   3.080   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.336  -0.770   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.002   0.000   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
CONECT    1   11                                                            
CONECT    2   11                                                            
CONECT    3   12                                                            
CONECT    4   15                                                            
CONECT    5    6    8                                                       
CONECT    6    5   12                                                       
CONECT    7    9   13                                                       
CONECT    8    5   15                                                       
CONECT    9    7   15                                                       
CONECT   10   13   14                                                       
CONECT   11    1    2   13                                                  
CONECT   12    3    6   14                                                  
CONECT   13    7   10   11                                                  
CONECT   14   10   12   15                                                  
CONECT   15    4    8    9   14                                             
MASTER        0    0    0    0    0    0    0    0   15    0   32    0
END

COMPND    HMDB0038118
HETATM    1  C1  UNL     1      -1.473   2.758   0.571  1.00  0.00           C  
HETATM    2  C2  UNL     1      -1.736   1.480   0.371  1.00  0.00           C  
HETATM    3  C3  UNL     1      -3.103   1.008   0.691  1.00  0.00           C  
HETATM    4  C4  UNL     1      -3.373  -0.393   0.280  1.00  0.00           C  
HETATM    5  C5  UNL     1      -2.463  -0.869  -0.839  1.00  0.00           C  
HETATM    6  C6  UNL     1      -1.053  -0.821  -0.295  1.00  0.00           C  
HETATM    7  C7  UNL     1      -1.020  -1.554   1.027  1.00  0.00           C  
HETATM    8  C8  UNL     1      -0.059  -1.481  -1.206  1.00  0.00           C  
HETATM    9  C9  UNL     1       1.178  -0.681  -1.450  1.00  0.00           C  
HETATM   10  C10 UNL     1       1.667   0.041  -0.248  1.00  0.00           C  
HETATM   11  C11 UNL     1       2.946   0.104   0.078  1.00  0.00           C  
HETATM   12  C12 UNL     1       3.995  -0.546  -0.739  1.00  0.00           C  
HETATM   13  C13 UNL     1       3.355   0.846   1.298  1.00  0.00           C  
HETATM   14  C14 UNL     1       0.636   0.714   0.605  1.00  0.00           C  
HETATM   15  C15 UNL     1      -0.662   0.625  -0.150  1.00  0.00           C  
HETATM   16  H1  UNL     1      -2.251   3.396   0.953  1.00  0.00           H  
HETATM   17  H2  UNL     1      -0.498   3.202   0.366  1.00  0.00           H  
HETATM   18  H3  UNL     1      -3.245   1.087   1.791  1.00  0.00           H  
HETATM   19  H4  UNL     1      -3.853   1.676   0.186  1.00  0.00           H  
HETATM   20  H5  UNL     1      -3.251  -1.073   1.149  1.00  0.00           H  
HETATM   21  H6  UNL     1      -4.410  -0.479  -0.098  1.00  0.00           H  
HETATM   22  H7  UNL     1      -2.768  -1.871  -1.161  1.00  0.00           H  
HETATM   23  H8  UNL     1      -2.500  -0.122  -1.673  1.00  0.00           H  
HETATM   24  H9  UNL     1      -0.023  -1.999   1.242  1.00  0.00           H  
HETATM   25  H10 UNL     1      -1.727  -2.412   0.925  1.00  0.00           H  
HETATM   26  H11 UNL     1      -1.344  -0.926   1.877  1.00  0.00           H  
HETATM   27  H12 UNL     1      -0.533  -1.687  -2.187  1.00  0.00           H  
HETATM   28  H13 UNL     1       0.253  -2.491  -0.816  1.00  0.00           H  
HETATM   29  H14 UNL     1       1.993  -1.407  -1.742  1.00  0.00           H  
HETATM   30  H15 UNL     1       1.079  -0.011  -2.330  1.00  0.00           H  
HETATM   31  H16 UNL     1       4.031  -1.621  -0.403  1.00  0.00           H  
HETATM   32  H17 UNL     1       3.794  -0.464  -1.828  1.00  0.00           H  
HETATM   33  H18 UNL     1       4.972  -0.082  -0.497  1.00  0.00           H  
HETATM   34  H19 UNL     1       2.579   0.844   2.088  1.00  0.00           H  
HETATM   35  H20 UNL     1       3.566   1.903   0.990  1.00  0.00           H  
HETATM   36  H21 UNL     1       4.257   0.374   1.756  1.00  0.00           H  
HETATM   37  H22 UNL     1       0.600   0.174   1.576  1.00  0.00           H  
HETATM   38  H23 UNL     1       0.884   1.769   0.795  1.00  0.00           H  
HETATM   39  H24 UNL     1      -0.438   0.991  -1.195  1.00  0.00           H  
CONECT    1    2    2   16   17
CONECT    2    3   15
CONECT    3    4   18   19
CONECT    4    5   20   21
CONECT    5    6   22   23
CONECT    6    7    8   15
CONECT    7   24   25   26
CONECT    8    9   27   28
CONECT    9   10   29   30
CONECT   10   11   11   14
CONECT   11   12   13
CONECT   12   31   32   33
CONECT   13   34   35   36
CONECT   14   15   37   38
CONECT   15   39
END

HMDB0038118
     RDKit          3D
gamma-Selinene
 39 40  0  0  0  0  0  0  0  0999 V2000
   -1.4734    2.7582    0.5713 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7363    1.4798    0.3715 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1028    1.0079    0.6914 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3733   -0.3926    0.2803 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4625   -0.8687   -0.8393 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0530   -0.8211   -0.2955 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0204   -1.5545    1.0267 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0587   -1.4810   -1.2065 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1779   -0.6812   -1.4501 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6666    0.0412   -0.2477 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9458    0.1044    0.0783 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9952   -0.5464   -0.7391 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3553    0.8455    1.2984 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6359    0.7144    0.6051 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6623    0.6249   -0.1505 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2505    3.3963    0.9528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4982    3.2021    0.3662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2449    1.0871    1.7908 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8526    1.6756    0.1856 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2513   -1.0734    1.1493 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4100   -0.4791   -0.0978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7681   -1.8705   -1.1606 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5005   -0.1224   -1.6730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0229   -1.9994    1.2418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7273   -2.4118    0.9249 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3438   -0.9261    1.8766 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5326   -1.6875   -2.1867 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2535   -2.4911   -0.8160 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9930   -1.4069   -1.7415 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0786   -0.0106   -2.3297 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0306   -1.6207   -0.4029 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7942   -0.4644   -1.8285 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9722   -0.0823   -0.4975 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5789    0.8438    2.0880 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5660    1.9025    0.9900 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2566    0.3744    1.7558 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5996    0.1741    1.5763 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8836    1.7687    0.7947 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4381    0.9908   -1.1952 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  3
 11 12  1  0
 11 13  1  0
 10 14  1  0
 14 15  1  0
 15  2  1  0
 15  6  1  0
  1 16  1  0
  1 17  1  0
  3 18  1  0
  3 19  1  0
  4 20  1  0
  4 21  1  0
  5 22  1  0
  5 23  1  0
  7 24  1  0
  7 25  1  0
  7 26  1  0
  8 27  1  0
  8 28  1  0
  9 29  1  0
  9 30  1  0
 12 31  1  0
 12 32  1  0
 12 33  1  0
 13 34  1  0
 13 35  1  0
 13 36  1  0
 14 37  1  0
 14 38  1  0
 15 39  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
g-Selinene	Generator
Γ-selinene	Generator
4(15),7(11)-Selinadiene	HMDB
Eudesma-4(14),7(11)-diene	HMDB
Eudesma-4(15),7(11)-diene	HMDB
Selina-4(14),7(11)-diene	HMDB
Selina-4(15),7(11)-diene	HMDB

Chemical Formula

C₁₅H₂₄

Average Molecular Weight

204.3511

Monoisotopic Molecular Weight

204.187800768

IUPAC Name

4a-methyl-1-methylidene-7-(propan-2-ylidene)-decahydronaphthalene

Traditional Name

4a-methyl-1-methylidene-7-(propan-2-ylidene)-hexahydro-2H-naphthalene

CAS Registry Number

515-17-3

SMILES

CC(C)=C1CCC2(C)CCCC(=C)C2C1

InChI Identifier

InChI=1S/C15H24/c1-11(2)13-7-9-15(4)8-5-6-12(3)14(15)10-13/h14H,3,5-10H2,1-2,4H3

InChI Key

RMZHSBMIZBMVMN-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Sesquiterpenoids

Alternative Parents

Substituents

Sesquiterpenoid
Branched unsaturated hydrocarbon
Polycyclic hydrocarbon
Cyclic olefin
Unsaturated aliphatic hydrocarbon
Unsaturated hydrocarbon
Olefin
Hydrocarbon
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Ontology

Cellular substructure

Membrane (HMDB: HMDB0038118)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0038118)

Source

Endogenous

Endogenous (HMDB: HMDB0038118)

Plant

Plant (HMDB: HMDB0038118)

Animal

Animal (HMDB: HMDB0038118)

Exogenous

Food

Food (HMDB: HMDB0038118)

Herb and spice

Spice

Wild celery (FooDB: FOOD00015)
Ginger (FooDB: FOOD00206)

Fruit

Citrus

Lime (FooDB: FOOD00053)
Mandarin orange (Clementine, Tangerine) (FooDB: FOOD00056)

Beverage

Alcoholic beverage

Alcoholic beverages (FooDB: FOOD00854)

Fat and oil

Fats and oils (FooDB: FOOD00864)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid peroxidation (HMDB: HMDB0038118)

Biochemical process

Fatty acid metabolism (HMDB: HMDB0038118)

Cellular process

Cell signaling (HMDB: HMDB0038118)

Biochemical pathway

Lipid metabolism pathway (HMDB: HMDB0038118)

Role

Biological role

Membrane stabilizer (HMDB: HMDB0038118)

Nutrient

Nutrient (HMDB: HMDB0038118)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0038118)

Emulsifier (HMDB: HMDB0038118)

Physical Properties

State

Not Available

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	269.00 to 270.00 °C. @ 760.00 mm Hg	The Good Scents Company Information System
Water Solubility	0.039 mg/L @ 25 °C (est)	The Good Scents Company Information System
LogP	6.729 (est)	The Good Scents Company Information System

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.017 g/L	ALOGPS
logP	5.27	ALOGPS
logP	4.48	ChemAxon
logS	-4.1	ALOGPS
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	0	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	0 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	67.19 m³·mol⁻¹	ChemAxon
Polarizability	26.15 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	149.635	31661259
DarkChem	[M-H]-	146.255	31661259
DeepCCS	[M+H]+	152.645	30932474
DeepCCS	[M-H]-	150.287	30932474
DeepCCS	[M-2H]-	185.261	30932474
DeepCCS	[M+Na]+	160.73	30932474
AllCCS	[M+H]+	149.1	32859911
AllCCS	[M+H-H2O]+	145.2	32859911
AllCCS	[M+NH4]+	152.8	32859911
AllCCS	[M+Na]+	153.9	32859911
AllCCS	[M-H]-	157.5	32859911
AllCCS	[M+Na-2H]-	158.1	32859911
AllCCS	[M+HCOO]-	158.9	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
gamma-Selinene	CC(C)=C1CCC2(C)CCCC(=C)C2C1	1756.4	Standard polar	33892256
gamma-Selinene	CC(C)=C1CCC2(C)CCCC(=C)C2C1	1486.9	Standard non polar	33892256
gamma-Selinene	CC(C)=C1CCC2(C)CCCC(=C)C2C1	1521.2	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 - gamma-Selinene GC-MS (Non-derivatized) - 70eV, Positive	splash10-009i-0900000000-e94fc3c0585d1f975928	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - gamma-Selinene GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - gamma-Selinene 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 - gamma-Selinene 10V, Positive-QTOF	splash10-0a4i-1590000000-c84f3ccccd88f2d594dd	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - gamma-Selinene 20V, Positive-QTOF	splash10-0c09-3920000000-2983fe6fdd13a4c267c9	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - gamma-Selinene 40V, Positive-QTOF	splash10-00kr-6900000000-96ca17613d9b727076d4	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - gamma-Selinene 10V, Negative-QTOF	splash10-0udi-0090000000-f9903e0c38590802f0a1	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - gamma-Selinene 20V, Negative-QTOF	splash10-0udi-0290000000-5367ee00d1cc75f8e8ae	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - gamma-Selinene 40V, Negative-QTOF	splash10-000i-1900000000-57cc0427d4db0d3c1755	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - gamma-Selinene 10V, Negative-QTOF	splash10-0udi-0090000000-7ccf03fa1149a1e9f55f	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - gamma-Selinene 20V, Negative-QTOF	splash10-0udi-0090000000-7ccf03fa1149a1e9f55f	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - gamma-Selinene 40V, Negative-QTOF	splash10-0udi-0390000000-7cfe3078bb17f36a6632	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - gamma-Selinene 10V, Positive-QTOF	splash10-03di-0900000000-5a3afc455e3d819ea51b	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - gamma-Selinene 20V, Positive-QTOF	splash10-05d0-4900000000-1310fb12a990f3d0a784	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - gamma-Selinene 40V, Positive-QTOF	splash10-05r3-9200000000-3c1b79e4713e0c34a677	2021-09-24	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

FDB017343

KNApSAcK ID

C00012714

Chemspider ID

454753

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

521334

PDB ID

Not Available

ChEBI ID

167347

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

rw1104381

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. [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. 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. 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) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. 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 gamma-Selinene (HMDB0038118)

MOL for HMDB0038118 (gamma-Selinene)

3D MOL for HMDB0038118 (gamma-Selinene)

3D SDF for HMDB0038118 (gamma-Selinene)

3D-SDF for HMDB0038118 (gamma-Selinene)

PDB for HMDB0038118 (gamma-Selinene)

3D PDB for HMDB0038118 (gamma-Selinene)

SMILES for HMDB0038118 (gamma-Selinene)

INCHI for HMDB0038118 (gamma-Selinene)

Structure for HMDB0038118 (gamma-Selinene)

3D Structure for HMDB0038118 (gamma-Selinene)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

GC-MS Spectra

MS/MS Spectra