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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 21:13:03 UTC

Update Date

2022-03-07 02:54:48 UTC

HMDB ID

HMDB0036154

Secondary Accession Numbers

HMDB36154

Metabolite Identification

Common Name

(Z)-2,6,10-Bisabolatriene

Description

(Z)-2,6,10-Bisabolatriene belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. Thus, (Z)-2,6,10-bisabolatriene is considered to be an isoprenoid. Based on a literature review a small amount of articles have been published on (Z)-2,6,10-Bisabolatriene.

Structure

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

HMDB0036154
     RDKit          3D
(Z)-2,6,10-Bisabolatriene
 39 39  0  0  0  0  0  0  0  0999 V2000
    5.1155   -0.9896    0.7429 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8859   -0.2001    0.4125 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5646    0.9215    1.3235 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1817   -0.5399   -0.6397 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9442    0.1576   -1.0779 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8304   -0.8917   -1.0501 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4613   -0.2924   -1.4751 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5942    0.3325   -2.8452 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5018   -0.3033   -0.6543 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7810    0.3302   -1.1675 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5175    0.8765    0.0044 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5535    0.1998    1.1412 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2947    0.7703    2.2912 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8474   -1.1067    1.1977 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4354   -0.8997    0.6996 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9980   -0.4778    0.3055 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2116   -1.1042    1.8518 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0534   -2.0061    0.2779 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0196    1.7428    0.8686 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0311    0.5442    2.2394 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5192    1.3545    1.7214 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4773   -1.3758   -1.2642 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6876    1.0392   -0.5018 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0068    0.4797   -2.1529 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1044   -1.7675   -1.6727 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8052   -1.2426   -0.0011 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5511    0.0469   -3.3184 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6215    1.4283   -2.7050 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2156   -0.0120   -3.5068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5268    1.1786   -1.8334 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4149   -0.3956   -1.6872 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0158    1.8244   -0.0930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3747    0.7770    2.0124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9488    1.8043    2.5331 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1207    0.1682    3.2172 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8777   -1.5449    2.2091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3252   -1.8249    0.4686 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9284   -0.2414    1.4278 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9597   -1.9132    0.7003 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 15  9  1  0
  1 16  1  0
  1 17  1  0
  1 18  1  0
  3 19  1  0
  3 20  1  0
  3 21  1  0
  4 22  1  0
  5 23  1  0
  5 24  1  0
  6 25  1  0
  6 26  1  0
  8 27  1  0
  8 28  1  0
  8 29  1  0
 10 30  1  0
 10 31  1  0
 11 32  1  0
 13 33  1  0
 13 34  1  0
 13 35  1  0
 14 36  1  0
 14 37  1  0
 15 38  1  0
 15 39  1  0
M  END


  Mrv1652303202019022D          

 15 15  0  0  0  0            999 V2000
    1.7734    0.6180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0309    0.2055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0309   -0.6180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3709   -1.0305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3709   -1.8555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1133    0.6180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3709    0.2055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3709   -0.6180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1133   -1.0305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7734   -0.6180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7734    0.2055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5159    0.6180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0309    1.8555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7734    1.4430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5159    1.8555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1 14  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  8  2  0  0  0  0
  6  7  1  0  0  0  0
  6 11  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0036154

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(C)=CCC\C(C)=C1/CCC(C)=CC1

> <INCHI_IDENTIFIER>
InChI=1S/C15H24/c1-12(2)6-5-7-14(4)15-10-8-13(3)9-11-15/h6,8H,5,7,9-11H2,1-4H3/b15-14-

> <INCHI_KEY>
XBGUIVFBMBVUEG-PFONDFGASA-N

> <FORMULA>
C15H24

> <MOLECULAR_WEIGHT>
204.3511

> <EXACT_MASS>
204.187800768

> <JCHEM_ACCEPTOR_COUNT>
0

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
26.868979322773733

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(4E)-1-methyl-4-(6-methylhept-5-en-2-ylidene)cyclohex-1-ene

> <ALOGPS_LOGP>
5.88

> <JCHEM_LOGP>
4.777935431666666

> <ALOGPS_LOGS>
-3.55

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_POLAR_SURFACE_AREA>
0.0

> <JCHEM_REFRACTIVITY>
71.08879999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.82e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(E)-gamma-bisabolene

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0036154
     RDKit          3D
(Z)-2,6,10-Bisabolatriene
 39 39  0  0  0  0  0  0  0  0999 V2000
    5.1155   -0.9896    0.7429 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8859   -0.2001    0.4125 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5646    0.9215    1.3235 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1817   -0.5399   -0.6397 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9442    0.1576   -1.0779 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8304   -0.8917   -1.0501 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4613   -0.2924   -1.4751 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5942    0.3325   -2.8452 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5018   -0.3033   -0.6543 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7810    0.3302   -1.1675 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5175    0.8765    0.0044 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5535    0.1998    1.1412 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2947    0.7703    2.2912 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8474   -1.1067    1.1977 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4354   -0.8997    0.6996 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9980   -0.4778    0.3055 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2116   -1.1042    1.8518 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0534   -2.0061    0.2779 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0196    1.7428    0.8686 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0311    0.5442    2.2394 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5192    1.3545    1.7214 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4773   -1.3758   -1.2642 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6876    1.0392   -0.5018 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0068    0.4797   -2.1529 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1044   -1.7675   -1.6727 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8052   -1.2426   -0.0011 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5511    0.0469   -3.3184 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6215    1.4283   -2.7050 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2156   -0.0120   -3.5068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5268    1.1786   -1.8334 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4149   -0.3956   -1.6872 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0158    1.8244   -0.0930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3747    0.7770    2.0124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9488    1.8043    2.5331 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1207    0.1682    3.2172 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8777   -1.5449    2.2091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3252   -1.8249    0.4686 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9284   -0.2414    1.4278 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9597   -1.9132    0.7003 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 15  9  1  0
  1 16  1  0
  1 17  1  0
  1 18  1  0
  3 19  1  0
  3 20  1  0
  3 21  1  0
  4 22  1  0
  5 23  1  0
  5 24  1  0
  6 25  1  0
  6 26  1  0
  8 27  1  0
  8 28  1  0
  8 29  1  0
 10 30  1  0
 10 31  1  0
 11 32  1  0
 13 33  1  0
 13 34  1  0
 13 35  1  0
 14 36  1  0
 14 37  1  0
 15 38  1  0
 15 39  1  0
M  END

HEADER    PROTEIN                                 20-MAR-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-MAR-20         0                                  
HETATM    1  C   UNK     0       3.310   1.154   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.924   0.384   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.924  -1.154   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.692  -1.924   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.692  -3.464   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.078   1.154   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.692   0.384   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.692  -1.154   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.078  -1.924   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -3.310  -1.154   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -3.310   0.384   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -4.696   1.154   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.924   3.464   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.310   2.694   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.696   3.464   0.000  0.00  0.00           C+0
CONECT    1    2   14                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    8                                                  
CONECT    5    4                                                            
CONECT    6    7   11                                                       
CONECT    7    6    8                                                       
CONECT    8    4    7    9                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11    6   10   12                                                  
CONECT   12   11                                                            
CONECT   13   14                                                            
CONECT   14    1   13   15                                                  
CONECT   15   14                                                            
MASTER        0    0    0    0    0    0    0    0   15    0   30    0
END

COMPND    HMDB0036154
HETATM    1  C1  UNL     1       5.115  -0.990   0.743  1.00  0.00           C  
HETATM    2  C2  UNL     1       3.886  -0.200   0.412  1.00  0.00           C  
HETATM    3  C3  UNL     1       3.565   0.921   1.323  1.00  0.00           C  
HETATM    4  C4  UNL     1       3.182  -0.540  -0.640  1.00  0.00           C  
HETATM    5  C5  UNL     1       1.944   0.158  -1.078  1.00  0.00           C  
HETATM    6  C6  UNL     1       0.830  -0.892  -1.050  1.00  0.00           C  
HETATM    7  C7  UNL     1      -0.461  -0.292  -1.475  1.00  0.00           C  
HETATM    8  C8  UNL     1      -0.594   0.332  -2.845  1.00  0.00           C  
HETATM    9  C9  UNL     1      -1.502  -0.303  -0.654  1.00  0.00           C  
HETATM   10  C10 UNL     1      -2.781   0.330  -1.167  1.00  0.00           C  
HETATM   11  C11 UNL     1      -3.518   0.876   0.004  1.00  0.00           C  
HETATM   12  C12 UNL     1      -3.553   0.200   1.141  1.00  0.00           C  
HETATM   13  C13 UNL     1      -4.295   0.770   2.291  1.00  0.00           C  
HETATM   14  C14 UNL     1      -2.847  -1.107   1.198  1.00  0.00           C  
HETATM   15  C15 UNL     1      -1.435  -0.900   0.700  1.00  0.00           C  
HETATM   16  H1  UNL     1       5.998  -0.478   0.306  1.00  0.00           H  
HETATM   17  H2  UNL     1       5.212  -1.104   1.852  1.00  0.00           H  
HETATM   18  H3  UNL     1       5.053  -2.006   0.278  1.00  0.00           H  
HETATM   19  H4  UNL     1       3.020   1.743   0.869  1.00  0.00           H  
HETATM   20  H5  UNL     1       3.031   0.544   2.239  1.00  0.00           H  
HETATM   21  H6  UNL     1       4.519   1.355   1.721  1.00  0.00           H  
HETATM   22  H7  UNL     1       3.477  -1.376  -1.264  1.00  0.00           H  
HETATM   23  H8  UNL     1       1.688   1.039  -0.502  1.00  0.00           H  
HETATM   24  H9  UNL     1       2.007   0.480  -2.153  1.00  0.00           H  
HETATM   25  H10 UNL     1       1.104  -1.767  -1.673  1.00  0.00           H  
HETATM   26  H11 UNL     1       0.805  -1.243  -0.001  1.00  0.00           H  
HETATM   27  H12 UNL     1      -1.551   0.047  -3.318  1.00  0.00           H  
HETATM   28  H13 UNL     1      -0.621   1.428  -2.705  1.00  0.00           H  
HETATM   29  H14 UNL     1       0.216  -0.012  -3.507  1.00  0.00           H  
HETATM   30  H15 UNL     1      -2.527   1.179  -1.833  1.00  0.00           H  
HETATM   31  H16 UNL     1      -3.415  -0.396  -1.687  1.00  0.00           H  
HETATM   32  H17 UNL     1      -4.016   1.824  -0.093  1.00  0.00           H  
HETATM   33  H18 UNL     1      -5.375   0.777   2.012  1.00  0.00           H  
HETATM   34  H19 UNL     1      -3.949   1.804   2.533  1.00  0.00           H  
HETATM   35  H20 UNL     1      -4.121   0.168   3.217  1.00  0.00           H  
HETATM   36  H21 UNL     1      -2.878  -1.545   2.209  1.00  0.00           H  
HETATM   37  H22 UNL     1      -3.325  -1.825   0.469  1.00  0.00           H  
HETATM   38  H23 UNL     1      -0.928  -0.241   1.428  1.00  0.00           H  
HETATM   39  H24 UNL     1      -0.960  -1.913   0.700  1.00  0.00           H  
CONECT    1    2   16   17   18
CONECT    2    3    4    4
CONECT    3   19   20   21
CONECT    4    5   22
CONECT    5    6   23   24
CONECT    6    7   25   26
CONECT    7    8    9    9
CONECT    8   27   28   29
CONECT    9   10   15
CONECT   10   11   30   31
CONECT   11   12   12   32
CONECT   12   13   14
CONECT   13   33   34   35
CONECT   14   15   36   37
CONECT   15   38   39
END

HMDB0036154
     RDKit          3D
(Z)-2,6,10-Bisabolatriene
 39 39  0  0  0  0  0  0  0  0999 V2000
    5.1155   -0.9896    0.7429 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8859   -0.2001    0.4125 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5646    0.9215    1.3235 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1817   -0.5399   -0.6397 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9442    0.1576   -1.0779 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8304   -0.8917   -1.0501 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4613   -0.2924   -1.4751 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5942    0.3325   -2.8452 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5018   -0.3033   -0.6543 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7810    0.3302   -1.1675 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5175    0.8765    0.0044 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5535    0.1998    1.1412 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2947    0.7703    2.2912 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8474   -1.1067    1.1977 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4354   -0.8997    0.6996 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9980   -0.4778    0.3055 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2116   -1.1042    1.8518 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0534   -2.0061    0.2779 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0196    1.7428    0.8686 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0311    0.5442    2.2394 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5192    1.3545    1.7214 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4773   -1.3758   -1.2642 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6876    1.0392   -0.5018 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0068    0.4797   -2.1529 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1044   -1.7675   -1.6727 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8052   -1.2426   -0.0011 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5511    0.0469   -3.3184 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6215    1.4283   -2.7050 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2156   -0.0120   -3.5068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5268    1.1786   -1.8334 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4149   -0.3956   -1.6872 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0158    1.8244   -0.0930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3747    0.7770    2.0124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9488    1.8043    2.5331 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1207    0.1682    3.2172 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8777   -1.5449    2.2091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3252   -1.8249    0.4686 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9284   -0.2414    1.4278 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9597   -1.9132    0.7003 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 15  9  1  0
  1 16  1  0
  1 17  1  0
  1 18  1  0
  3 19  1  0
  3 20  1  0
  3 21  1  0
  4 22  1  0
  5 23  1  0
  5 24  1  0
  6 25  1  0
  6 26  1  0
  8 27  1  0
  8 28  1  0
  8 29  1  0
 10 30  1  0
 10 31  1  0
 11 32  1  0
 13 33  1  0
 13 34  1  0
 13 35  1  0
 14 36  1  0
 14 37  1  0
 15 38  1  0
 15 39  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
(Z)-laquo gammaraquo -Bisabolene	HMDB
(e)-g-Bisabolene	Generator
(e)-Γ-bisabolene	Generator

Chemical Formula

C₁₅H₂₄

Average Molecular Weight

204.3511

Monoisotopic Molecular Weight

204.187800768

IUPAC Name

(4E)-1-methyl-4-(6-methylhept-5-en-2-ylidene)cyclohex-1-ene

Traditional Name

(E)-gamma-bisabolene

CAS Registry Number

13062-00-5

SMILES

CC(C)=CCC\C(C)=C1/CCC(C)=CC1

InChI Identifier

InChI=1S/C15H24/c1-12(2)6-5-7-14(4)15-10-8-13(3)9-11-15/h6,8H,5,7,9-11H2,1-4H3/b15-14-

InChI Key

XBGUIVFBMBVUEG-PFONDFGASA-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

Bisabolane sesquiterpenoid
Sesquiterpenoid
Branched unsaturated hydrocarbon
Cycloalkene
Cyclic olefin
Unsaturated aliphatic hydrocarbon
Unsaturated hydrocarbon
Olefin
Hydrocarbon
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic homomonocyclic compounds

External Descriptors

gamma-bisabolene (CHEBI:49239 )
Bisabolane sesquiterpenoids (LMPR0103060005 )

Ontology

Not Available

Carrot (FooDB: FOOD00245)
Wild carrot (FooDB: FOOD00072)

Process

Not Available

Role

Not Available

Physical Properties

State

Not Available

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	280.00 to 281.00 °C. @ 760.00 mm Hg	The Good Scents Company Information System
Water Solubility	0.009 mg/L @ 25 °C (est)	The Good Scents Company Information System
LogP	6.704 (est)	The Good Scents Company Information System

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.058 g/L	ALOGPS
logP	5.88	ALOGPS
logP	4.78	ChemAxon
logS	-3.6	ALOGPS
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	0	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	0 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	71.09 m³·mol⁻¹	ChemAxon
Polarizability	26.87 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

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	153.86	31661259
DarkChem	[M-H]-	148.808	31661259
DeepCCS	[M+H]+	155.006	30932474
DeepCCS	[M-H]-	152.648	30932474
DeepCCS	[M-2H]-	186.696	30932474
DeepCCS	[M+Na]+	161.461	30932474
AllCCS	[M+H]+	150.0	32859911
AllCCS	[M+H-H2O]+	146.0	32859911
AllCCS	[M+NH4]+	153.6	32859911
AllCCS	[M+Na]+	154.7	32859911
AllCCS	[M-H]-	155.5	32859911
AllCCS	[M+Na-2H]-	156.2	32859911
AllCCS	[M+HCOO]-	157.0	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
(Z)-2,6,10-Bisabolatriene	CC(C)=CCC\C(C)=C1/CCC(C)=CC1	1742.7	Standard polar	33892256
(Z)-2,6,10-Bisabolatriene	CC(C)=CCC\C(C)=C1/CCC(C)=CC1	1517.7	Standard non polar	33892256
(Z)-2,6,10-Bisabolatriene	CC(C)=CCC\C(C)=C1/CCC(C)=CC1	1539.2	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 - (Z)-2,6,10-Bisabolatriene GC-MS (Non-derivatized) - 70eV, Positive	splash10-00ku-7900000000-f0996e8952fb933ec1a1	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (Z)-2,6,10-Bisabolatriene GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (Z)-2,6,10-Bisabolatriene 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 - (Z)-2,6,10-Bisabolatriene 10V, Positive-QTOF	splash10-0a4i-3790000000-d9bfff51a973f095b0f7	2016-06-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (Z)-2,6,10-Bisabolatriene 20V, Positive-QTOF	splash10-0a59-6910000000-b3ba4af91c15ca820f02	2016-06-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (Z)-2,6,10-Bisabolatriene 40V, Positive-QTOF	splash10-0gb9-9400000000-c572c8e71209344306bb	2016-06-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (Z)-2,6,10-Bisabolatriene 10V, Negative-QTOF	splash10-0udi-0090000000-b9ec3a3fca68549c9c68	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (Z)-2,6,10-Bisabolatriene 20V, Negative-QTOF	splash10-0udi-0190000000-c4fd97be688246991a84	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (Z)-2,6,10-Bisabolatriene 40V, Negative-QTOF	splash10-0079-4900000000-85130b2dad3062d4c601	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (Z)-2,6,10-Bisabolatriene 10V, Positive-QTOF	splash10-0a59-9420000000-5092d8f0b03c4273c2ad	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (Z)-2,6,10-Bisabolatriene 20V, Positive-QTOF	splash10-00kg-9300000000-f48deeaf43b19cf036f5	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (Z)-2,6,10-Bisabolatriene 40V, Positive-QTOF	splash10-066u-9100000000-6e8c9fc99a0906a17458	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (Z)-2,6,10-Bisabolatriene 10V, Negative-QTOF	splash10-0udi-0090000000-7ccf03fa1149a1e9f55f	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (Z)-2,6,10-Bisabolatriene 20V, Negative-QTOF	splash10-0udi-0190000000-8f291e3c98cfd164ba30	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (Z)-2,6,10-Bisabolatriene 40V, Negative-QTOF	splash10-014i-5900000000-a8d4d6ee48d3fc56bc3f	2021-09-24	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Extracellular
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

KNApSAcK ID

Chemspider ID

KEGG Compound ID

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5352437

PDB ID

Not Available

ChEBI ID

49239

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

rw1389311

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 (Z)-2,6,10-Bisabolatriene (HMDB0036154)

MOL for HMDB0036154 ((Z)-2,6,10-Bisabolatriene)

3D MOL for HMDB0036154 ((Z)-2,6,10-Bisabolatriene)

3D SDF for HMDB0036154 ((Z)-2,6,10-Bisabolatriene)

3D-SDF for HMDB0036154 ((Z)-2,6,10-Bisabolatriene)

PDB for HMDB0036154 ((Z)-2,6,10-Bisabolatriene)

3D PDB for HMDB0036154 ((Z)-2,6,10-Bisabolatriene)

SMILES for HMDB0036154 ((Z)-2,6,10-Bisabolatriene)

INCHI for HMDB0036154 ((Z)-2,6,10-Bisabolatriene)

Structure for HMDB0036154 ((Z)-2,6,10-Bisabolatriene)

3D Structure for HMDB0036154 ((Z)-2,6,10-Bisabolatriene)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

GC-MS Spectra

MS/MS Spectra