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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 21:15:33 UTC

Update Date

2022-03-07 02:54:49 UTC

HMDB ID

HMDB0036200

Secondary Accession Numbers

HMDB36200

Metabolite Identification

Common Name

(R)-2,5,11-Bisabolatriene

Description

(R)-2,5,11-Bisabolatriene belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. Based on a literature review a small amount of articles have been published on (R)-2,5,11-Bisabolatriene.

Structure

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

HMDB0036200
     RDKit          3D
(R)-2,5,11-Bisabolatriene
 39 39  0  0  0  0  0  0  0  0999 V2000
   -4.4354   -0.4905    1.3757 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9160    0.3353    0.4731 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4290    0.3502   -0.9222 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8148    1.2618    0.8283 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5643    0.9834   -0.0338 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1751   -0.4192    0.2482 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0037   -0.9757   -0.4802 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1138   -2.4380    0.0426 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2334   -0.2513   -0.1363 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1892   -0.8752    0.5602 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4599   -0.1508    0.9203 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8620    0.5345   -0.3670 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2796    0.5071   -0.8166 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9201    1.1436   -1.0570 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5017    1.1410   -0.5565 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0447   -0.4838    2.3887 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2397   -1.1577    1.0898 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0138    1.3060   -1.0440 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5741    0.3659   -1.6259 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0870   -0.5136   -1.1383 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5746    1.1269    1.9025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0782    2.3260    0.6985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8011    1.7218    0.3264 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8045    1.2172   -1.0730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0973   -1.0625    0.1053 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0087   -0.4853    1.3677 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1271   -1.0508   -1.5586 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9588   -2.9488   -0.4229 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1508   -2.4121    1.1398 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8512   -2.9142   -0.2409 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1093   -1.8999    0.8941 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2399   -0.8420    1.2311 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2115    0.6414    1.6462 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3915   -0.1943   -1.6875 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6231    1.4945   -1.1556 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9173    0.1393    0.0025 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1231    1.6502   -1.9756 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8206    1.5166   -1.3454 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5347    1.8031    0.3516 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  2  0
 14 15  1  0
 15  9  1  0
  1 16  1  0
  1 17  1  0
  3 18  1  0
  3 19  1  0
  3 20  1  0
  4 21  1  0
  4 22  1  0
  5 23  1  0
  5 24  1  0
  6 25  1  0
  6 26  1  0
  7 27  1  0
  8 28  1  0
  8 29  1  0
  8 30  1  0
 10 31  1  0
 11 32  1  0
 11 33  1  0
 13 34  1  0
 13 35  1  0
 13 36  1  0
 14 37  1  0
 15 38  1  0
 15 39  1  0
M  END


  Mrv0541 05061308562D          

 15 15  0  0  0  0            999 V2000
    4.2868   -0.8250    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
   10.7171   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -1.6500    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
   10.0026   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  1  0  0  0  0
  7  5  1  0  0  0  0
 10  8  1  0  0  0  0
 11  9  1  0  0  0  0
 12  1  2  0  0  0  0
 12  2  1  0  0  0  0
 12  6  1  0  0  0  0
 13  3  1  0  0  0  0
 13  8  2  0  0  0  0
 13  9  1  0  0  0  0
 14  4  1  0  0  0  0
 14  7  1  0  0  0  0
 15 10  1  0  0  0  0
 15 11  2  0  0  0  0
 15 14  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0036200

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(CCCC(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/h8,11,14H,1,5-7,9-10H2,2-4H3

> <INCHI_KEY>
XISBISVWIJDEQH-UHFFFAOYSA-N

> <FORMULA>
C15H24

> <MOLECULAR_WEIGHT>
204.3511

> <EXACT_MASS>
204.187800768

> <JCHEM_ACCEPTOR_COUNT>
0

> <JCHEM_AVERAGE_POLARIZABILITY>
26.49872133675185

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1-methyl-4-(6-methylhept-6-en-2-yl)cyclohexa-1,4-diene

> <ALOGPS_LOGP>
6.07

> <JCHEM_LOGP>
4.879526926666667

> <ALOGPS_LOGS>
-4.37

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_POLAR_SURFACE_AREA>
0

> <JCHEM_REFRACTIVITY>
70.2829

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.81e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-methyl-4-(6-methylhept-6-en-2-yl)cyclohexa-1,4-diene

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0036200
     RDKit          3D
(R)-2,5,11-Bisabolatriene
 39 39  0  0  0  0  0  0  0  0999 V2000
   -4.4354   -0.4905    1.3757 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9160    0.3353    0.4731 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4290    0.3502   -0.9222 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8148    1.2618    0.8283 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5643    0.9834   -0.0338 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1751   -0.4192    0.2482 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0037   -0.9757   -0.4802 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1138   -2.4380    0.0426 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2334   -0.2513   -0.1363 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1892   -0.8752    0.5602 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4599   -0.1508    0.9203 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8620    0.5345   -0.3670 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2796    0.5071   -0.8166 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9201    1.1436   -1.0570 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5017    1.1410   -0.5565 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0447   -0.4838    2.3887 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2397   -1.1577    1.0898 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0138    1.3060   -1.0440 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5741    0.3659   -1.6259 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0870   -0.5136   -1.1383 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5746    1.1269    1.9025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0782    2.3260    0.6985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8011    1.7218    0.3264 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8045    1.2172   -1.0730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0973   -1.0625    0.1053 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0087   -0.4853    1.3677 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1271   -1.0508   -1.5586 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9588   -2.9488   -0.4229 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1508   -2.4121    1.1398 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8512   -2.9142   -0.2409 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1093   -1.8999    0.8941 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2399   -0.8420    1.2311 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2115    0.6414    1.6462 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3915   -0.1943   -1.6875 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6231    1.4945   -1.1556 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9173    0.1393    0.0025 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1231    1.6502   -1.9756 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8206    1.5166   -1.3454 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5347    1.8031    0.3516 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  2  0
 14 15  1  0
 15  9  1  0
  1 16  1  0
  1 17  1  0
  3 18  1  0
  3 19  1  0
  3 20  1  0
  4 21  1  0
  4 22  1  0
  5 23  1  0
  5 24  1  0
  6 25  1  0
  6 26  1  0
  7 27  1  0
  8 28  1  0
  8 29  1  0
  8 30  1  0
 10 31  1  0
 11 32  1  0
 11 33  1  0
 13 34  1  0
 13 35  1  0
 13 36  1  0
 14 37  1  0
 15 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       8.002  -1.540   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.336   0.770   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      20.005  -3.850   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      14.671   0.770   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      12.003  -0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.669  -1.540   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      13.337  -1.540   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      18.672  -1.540   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      17.338  -3.850   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      17.338  -0.770   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      16.004  -3.080   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.336  -0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      18.672  -3.080   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      14.671  -0.770   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      16.004  -1.540   0.000  0.00  0.00           C+0
CONECT    1   12                                                            
CONECT    2   12                                                            
CONECT    3   13                                                            
CONECT    4   14                                                            
CONECT    5    6    7                                                       
CONECT    6    5   12                                                       
CONECT    7    5   14                                                       
CONECT    8   10   13                                                       
CONECT    9   11   13                                                       
CONECT   10    8   15                                                       
CONECT   11    9   15                                                       
CONECT   12    1    2    6                                                  
CONECT   13    3    8    9                                                  
CONECT   14    4    7   15                                                  
CONECT   15   10   11   14                                                  
MASTER        0    0    0    0    0    0    0    0   15    0   30    0
END

COMPND    HMDB0036200
HETATM    1  C1  UNL     1      -4.435  -0.490   1.376  1.00  0.00           C  
HETATM    2  C2  UNL     1      -3.916   0.335   0.473  1.00  0.00           C  
HETATM    3  C3  UNL     1      -4.429   0.350  -0.922  1.00  0.00           C  
HETATM    4  C4  UNL     1      -2.815   1.262   0.828  1.00  0.00           C  
HETATM    5  C5  UNL     1      -1.564   0.983  -0.034  1.00  0.00           C  
HETATM    6  C6  UNL     1      -1.175  -0.419   0.248  1.00  0.00           C  
HETATM    7  C7  UNL     1      -0.004  -0.976  -0.480  1.00  0.00           C  
HETATM    8  C8  UNL     1       0.114  -2.438   0.043  1.00  0.00           C  
HETATM    9  C9  UNL     1       1.233  -0.251  -0.136  1.00  0.00           C  
HETATM   10  C10 UNL     1       2.189  -0.875   0.560  1.00  0.00           C  
HETATM   11  C11 UNL     1       3.460  -0.151   0.920  1.00  0.00           C  
HETATM   12  C12 UNL     1       3.862   0.534  -0.367  1.00  0.00           C  
HETATM   13  C13 UNL     1       5.280   0.507  -0.817  1.00  0.00           C  
HETATM   14  C14 UNL     1       2.920   1.144  -1.057  1.00  0.00           C  
HETATM   15  C15 UNL     1       1.502   1.141  -0.556  1.00  0.00           C  
HETATM   16  H1  UNL     1      -4.045  -0.484   2.389  1.00  0.00           H  
HETATM   17  H2  UNL     1      -5.240  -1.158   1.090  1.00  0.00           H  
HETATM   18  H3  UNL     1      -5.014   1.306  -1.044  1.00  0.00           H  
HETATM   19  H4  UNL     1      -3.574   0.366  -1.626  1.00  0.00           H  
HETATM   20  H5  UNL     1      -5.087  -0.514  -1.138  1.00  0.00           H  
HETATM   21  H6  UNL     1      -2.575   1.127   1.902  1.00  0.00           H  
HETATM   22  H7  UNL     1      -3.078   2.326   0.698  1.00  0.00           H  
HETATM   23  H8  UNL     1      -0.801   1.722   0.326  1.00  0.00           H  
HETATM   24  H9  UNL     1      -1.805   1.217  -1.073  1.00  0.00           H  
HETATM   25  H10 UNL     1      -2.097  -1.063   0.105  1.00  0.00           H  
HETATM   26  H11 UNL     1      -1.009  -0.485   1.368  1.00  0.00           H  
HETATM   27  H12 UNL     1      -0.127  -1.051  -1.559  1.00  0.00           H  
HETATM   28  H13 UNL     1       0.959  -2.949  -0.423  1.00  0.00           H  
HETATM   29  H14 UNL     1       0.151  -2.412   1.140  1.00  0.00           H  
HETATM   30  H15 UNL     1      -0.851  -2.914  -0.241  1.00  0.00           H  
HETATM   31  H16 UNL     1       2.109  -1.900   0.894  1.00  0.00           H  
HETATM   32  H17 UNL     1       4.240  -0.842   1.231  1.00  0.00           H  
HETATM   33  H18 UNL     1       3.212   0.641   1.646  1.00  0.00           H  
HETATM   34  H19 UNL     1       5.392  -0.194  -1.687  1.00  0.00           H  
HETATM   35  H20 UNL     1       5.623   1.495  -1.156  1.00  0.00           H  
HETATM   36  H21 UNL     1       5.917   0.139   0.002  1.00  0.00           H  
HETATM   37  H22 UNL     1       3.123   1.650  -1.976  1.00  0.00           H  
HETATM   38  H23 UNL     1       0.821   1.517  -1.345  1.00  0.00           H  
HETATM   39  H24 UNL     1       1.535   1.803   0.352  1.00  0.00           H  
CONECT    1    2    2   16   17
CONECT    2    3    4
CONECT    3   18   19   20
CONECT    4    5   21   22
CONECT    5    6   23   24
CONECT    6    7   25   26
CONECT    7    8    9   27
CONECT    8   28   29   30
CONECT    9   10   10   15
CONECT   10   11   31
CONECT   11   12   32   33
CONECT   12   13   14   14
CONECT   13   34   35   36
CONECT   14   15   37
CONECT   15   38   39
END

HMDB0036200
     RDKit          3D
(R)-2,5,11-Bisabolatriene
 39 39  0  0  0  0  0  0  0  0999 V2000
   -4.4354   -0.4905    1.3757 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9160    0.3353    0.4731 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4290    0.3502   -0.9222 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8148    1.2618    0.8283 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5643    0.9834   -0.0338 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1751   -0.4192    0.2482 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0037   -0.9757   -0.4802 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1138   -2.4380    0.0426 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2334   -0.2513   -0.1363 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1892   -0.8752    0.5602 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4599   -0.1508    0.9203 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8620    0.5345   -0.3670 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2796    0.5071   -0.8166 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9201    1.1436   -1.0570 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5017    1.1410   -0.5565 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0447   -0.4838    2.3887 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2397   -1.1577    1.0898 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0138    1.3060   -1.0440 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5741    0.3659   -1.6259 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0870   -0.5136   -1.1383 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5746    1.1269    1.9025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0782    2.3260    0.6985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8011    1.7218    0.3264 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8045    1.2172   -1.0730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0973   -1.0625    0.1053 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0087   -0.4853    1.3677 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1271   -1.0508   -1.5586 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9588   -2.9488   -0.4229 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1508   -2.4121    1.1398 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8512   -2.9142   -0.2409 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1093   -1.8999    0.8941 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2399   -0.8420    1.2311 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2115    0.6414    1.6462 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3915   -0.1943   -1.6875 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6231    1.4945   -1.1556 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9173    0.1393    0.0025 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1231    1.6502   -1.9756 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8206    1.5166   -1.3454 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5347    1.8031    0.3516 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  2  0
 14 15  1  0
 15  9  1  0
  1 16  1  0
  1 17  1  0
  3 18  1  0
  3 19  1  0
  3 20  1  0
  4 21  1  0
  4 22  1  0
  5 23  1  0
  5 24  1  0
  6 25  1  0
  6 26  1  0
  7 27  1  0
  8 28  1  0
  8 29  1  0
  8 30  1  0
 10 31  1  0
 11 32  1  0
 11 33  1  0
 13 34  1  0
 13 35  1  0
 13 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
3-Methyl-4-[(e)-prop-1-enyl]cyclohexene	HMDB
beta-Curcumene	HMDB

Chemical Formula

C₁₅H₂₄

Average Molecular Weight

204.3511

Monoisotopic Molecular Weight

204.187800768

IUPAC Name

1-methyl-4-(6-methylhept-6-en-2-yl)cyclohexa-1,4-diene

Traditional Name

1-methyl-4-(6-methylhept-6-en-2-yl)cyclohexa-1,4-diene

CAS Registry Number

28976-67-2

SMILES

CC(CCCC(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/h8,11,14H,1,5-7,9-10H2,2-4H3

InChI Key

XISBISVWIJDEQH-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

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

Molecular Framework

Aliphatic homomonocyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cytoplasm (HMDB: HMDB0036200)
Cell membrane (HMDB: HMDB0036200)

Cellular substructure

Extracellular (HMDB: HMDB0036200)
Membrane (HMDB: HMDB0036200)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0036200)

Source

Endogenous

Endogenous (HMDB: HMDB0036200)

Plant

Plant (HMDB: HMDB0036200)

Animal

Animal (HMDB: HMDB0036200)

Exogenous

Food

Food (HMDB: HMDB0036200)

Herb and spice

Spice

Turmeric (FooDB: FOOD00068)

Herb

Lemon balm (FooDB: FOOD00108)

Herbs and Spices (FooDB: FOOD00866)

Vegetable

Root vegetable

Root vegetables (FooDB: FOOD00873)

Beverage

Beverages (FooDB: FOOD00870)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid peroxidation (HMDB: HMDB0036200)

Biochemical process

Fatty acid metabolism (HMDB: HMDB0036200)

Cellular process

Cell signaling (HMDB: HMDB0036200)

Biochemical pathway

Lipid metabolism pathway (HMDB: HMDB0036200)

Role

Biological role

Membrane stabilizer (HMDB: HMDB0036200)

Nutrient

Nutrient (HMDB: HMDB0036200)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0036200)

Emulsifier (HMDB: HMDB0036200)

Physical Properties

State

Not Available

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	273.00 to 275.00 °C. @ 760.00 mm Hg (est)	The Good Scents Company Information System
Water Solubility	0.012 mg/L @ 25 °C (est)	The Good Scents Company Information System
LogP	6.550 (est)	The Good Scents Company Information System

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.0088 g/L	ALOGPS
logP	6.07	ALOGPS
logP	4.88	ChemAxon
logS	-4.4	ALOGPS
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	0	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	0 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	70.28 m³·mol⁻¹	ChemAxon
Polarizability	26.5 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]+	151.082	31661259
DarkChem	[M-H]-	148.349	31661259
DeepCCS	[M+H]+	151.902	30932474
DeepCCS	[M-H]-	149.545	30932474
DeepCCS	[M-2H]-	184.327	30932474
DeepCCS	[M+Na]+	159.727	30932474
AllCCS	[M+H]+	150.7	32859911
AllCCS	[M+H-H2O]+	146.8	32859911
AllCCS	[M+NH4]+	154.4	32859911
AllCCS	[M+Na]+	155.5	32859911
AllCCS	[M-H]-	156.6	32859911
AllCCS	[M+Na-2H]-	157.4	32859911
AllCCS	[M+HCOO]-	158.4	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
(R)-2,5,11-Bisabolatriene	CC(CCCC(C)=C)C1=CCC(C)=CC1	1815.5	Standard polar	33892256
(R)-2,5,11-Bisabolatriene	CC(CCCC(C)=C)C1=CCC(C)=CC1	1487.8	Standard non polar	33892256
(R)-2,5,11-Bisabolatriene	CC(CCCC(C)=C)C1=CCC(C)=CC1	1481.5	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 - (R)-2,5,11-Bisabolatriene GC-MS (Non-derivatized) - 70eV, Positive	splash10-000m-9800000000-658cea59abdc0204600a	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (R)-2,5,11-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 - (R)-2,5,11-Bisabolatriene 10V, Positive-QTOF	splash10-0a4i-2690000000-2cd77d07b51076abc213	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (R)-2,5,11-Bisabolatriene 20V, Positive-QTOF	splash10-0a4r-5920000000-e143691e48a04d8f37f2	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (R)-2,5,11-Bisabolatriene 40V, Positive-QTOF	splash10-0gb9-9400000000-df0fe91c5c9056dc09f2	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (R)-2,5,11-Bisabolatriene 10V, Negative-QTOF	splash10-0udi-0090000000-6e33e9b31012b6d8bbae	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (R)-2,5,11-Bisabolatriene 20V, Negative-QTOF	splash10-0udi-0190000000-49fc3f438b5b47ee65e7	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (R)-2,5,11-Bisabolatriene 40V, Negative-QTOF	splash10-000i-4910000000-88c9cbc55390cb4e3e9e	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (R)-2,5,11-Bisabolatriene 10V, Negative-QTOF	splash10-0udi-0090000000-7ccf03fa1149a1e9f55f	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (R)-2,5,11-Bisabolatriene 20V, Negative-QTOF	splash10-0udi-0290000000-28f3bed447b457d8a54c	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (R)-2,5,11-Bisabolatriene 40V, Negative-QTOF	splash10-0udi-3490000000-96cf95b6478505cf0706	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (R)-2,5,11-Bisabolatriene 10V, Positive-QTOF	splash10-00xr-9510000000-c3ba8c4de7990c3471e8	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (R)-2,5,11-Bisabolatriene 20V, Positive-QTOF	splash10-00kf-9200000000-81c34ff7783d55b1f43f	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (R)-2,5,11-Bisabolatriene 40V, Positive-QTOF	splash10-0006-9200000000-a55117065bef06cb69fa	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

FDB015057

KNApSAcK ID

C00011630

Chemspider ID

4475314

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5316213

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

rw1561531

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 (R)-2,5,11-Bisabolatriene (HMDB0036200)

MOL for HMDB0036200 ((R)-2,5,11-Bisabolatriene)

3D MOL for HMDB0036200 ((R)-2,5,11-Bisabolatriene)

3D SDF for HMDB0036200 ((R)-2,5,11-Bisabolatriene)

3D-SDF for HMDB0036200 ((R)-2,5,11-Bisabolatriene)

PDB for HMDB0036200 ((R)-2,5,11-Bisabolatriene)

3D PDB for HMDB0036200 ((R)-2,5,11-Bisabolatriene)

SMILES for HMDB0036200 ((R)-2,5,11-Bisabolatriene)

INCHI for HMDB0036200 ((R)-2,5,11-Bisabolatriene)

Structure for HMDB0036200 ((R)-2,5,11-Bisabolatriene)

3D Structure for HMDB0036200 ((R)-2,5,11-Bisabolatriene)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

GC-MS Spectra

MS/MS Spectra