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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2012-09-11 23:02:40 UTC

Update Date

2022-03-07 02:55:30 UTC

HMDB ID

HMDB0037784

Secondary Accession Numbers

HMDB37784

Metabolite Identification

Common Name

(+)-alpha-Muurolene

Description

(+)-alpha-Muurolene 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 (+)-alpha-Muurolene.

Structure

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

HMDB0037784
     RDKit          3D
(+)-alpha-Muurolene
 39 40  0  0  0  0  0  0  0  0999 V2000
    3.1313   -2.3670    0.3680 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1859   -1.3096    0.0053 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8890   -1.3230    0.3112 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1363   -0.1580   -0.1549 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8177    1.1003    0.3477 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2792    1.0985    0.0800 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6733   -0.1235   -0.7580 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1025    2.2419   -0.2990 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8617    3.5191   -0.4478 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1510    2.1456   -0.7286 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9698    0.9193   -0.6188 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2811   -0.0838    0.2848 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0119   -1.3974    0.2561 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0436   -1.9826   -1.1408 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4708   -1.0753    0.6082 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3869   -3.0067   -0.5182 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1040   -1.8707    0.6427 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8420   -3.0018    1.2004 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4864   -2.1643    0.8658 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1556   -0.1319   -1.2711 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5724    1.1827    1.4463 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6883    2.0270   -0.3207 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7990    0.9337    1.0694 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7644   -0.1028   -0.8692 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2216   -0.0594   -1.7717 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1548    4.3648   -0.5933 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5828    3.4569   -1.2670 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3865    3.6720    0.5339 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5716    3.0379   -1.1831 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0144    0.4569   -1.6468 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9773    1.1101   -0.2077 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3503    0.3215    1.3166 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5898   -2.1265    0.9429 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8673   -1.5038   -1.7070 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3564   -3.0549   -1.0183 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0712   -1.8917   -1.6290 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9998   -0.7380   -0.3200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5261   -0.2036    1.3048 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9692   -1.9117    1.1048 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  5  8  1  0
  8  9  1  0
  8 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
  7  2  1  0
 12  4  1  0
  1 16  1  0
  1 17  1  0
  1 18  1  0
  3 19  1  0
  4 20  1  0
  5 21  1  0
  6 22  1  0
  6 23  1  0
  7 24  1  0
  7 25  1  0
  9 26  1  0
  9 27  1  0
  9 28  1  0
 10 29  1  0
 11 30  1  0
 11 31  1  0
 12 32  1  0
 13 33  1  0
 14 34  1  0
 14 35  1  0
 14 36  1  0
 15 37  1  0
 15 38  1  0
 15 39  1  0
M  END

Muurolene-alpha
  Mrv1572001071617132D          
  Mrv0541 01101312262D          
 15 16  0  0  0  0            999 V2000
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    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
    2.1434   -0.4125    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
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    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  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  2  7  1  0  0  0  0
  5  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  4 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
  8 15  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0037784

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(C)C1CC=C(C)C2CCC(C)=CC12

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

> <INCHI_KEY>
QMAYBMKBYCGXDH-UHFFFAOYSA-N

> <FORMULA>
C15H24

> <MOLECULAR_WEIGHT>
204.357

> <EXACT_MASS>
204.187800773

> <JCHEM_ACCEPTOR_COUNT>
0

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
26.347638921117014

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4,7-dimethyl-1-(propan-2-yl)-1,2,4a,5,6,8a-hexahydronaphthalene

> <ALOGPS_LOGP>
5.00

> <JCHEM_LOGP>
4.448347697666667

> <ALOGPS_LOGS>
-4.30

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_POLAR_SURFACE_AREA>
0.0

> <JCHEM_REFRACTIVITY>
68.5984

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.03e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
cadinene

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0037784
     RDKit          3D
(+)-alpha-Muurolene
 39 40  0  0  0  0  0  0  0  0999 V2000
    3.1313   -2.3670    0.3680 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1859   -1.3096    0.0053 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8890   -1.3230    0.3112 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1363   -0.1580   -0.1549 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8177    1.1003    0.3477 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2792    1.0985    0.0800 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6733   -0.1235   -0.7580 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1025    2.2419   -0.2990 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8617    3.5191   -0.4478 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1510    2.1456   -0.7286 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9698    0.9193   -0.6188 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2811   -0.0838    0.2848 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0119   -1.3974    0.2561 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0436   -1.9826   -1.1408 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4708   -1.0753    0.6082 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3869   -3.0067   -0.5182 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1040   -1.8707    0.6427 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8420   -3.0018    1.2004 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4864   -2.1643    0.8658 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1556   -0.1319   -1.2711 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5724    1.1827    1.4463 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6883    2.0270   -0.3207 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7990    0.9337    1.0694 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7644   -0.1028   -0.8692 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2216   -0.0594   -1.7717 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1548    4.3648   -0.5933 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5828    3.4569   -1.2670 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3865    3.6720    0.5339 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5716    3.0379   -1.1831 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0144    0.4569   -1.6468 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9773    1.1101   -0.2077 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3503    0.3215    1.3166 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5898   -2.1265    0.9429 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8673   -1.5038   -1.7070 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3564   -3.0549   -1.0183 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0712   -1.8917   -1.6290 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9998   -0.7380   -0.3200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5261   -0.2036    1.3048 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9692   -1.9117    1.1048 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  5  8  1  0
  8  9  1  0
  8 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
  7  2  1  0
 12  4  1  0
  1 16  1  0
  1 17  1  0
  1 18  1  0
  3 19  1  0
  4 20  1  0
  5 21  1  0
  6 22  1  0
  6 23  1  0
  7 24  1  0
  7 25  1  0
  9 26  1  0
  9 27  1  0
  9 28  1  0
 10 29  1  0
 11 30  1  0
 11 31  1  0
 12 32  1  0
 13 33  1  0
 14 34  1  0
 14 35  1  0
 14 36  1  0
 15 37  1  0
 15 38  1  0
 15 39  1  0
M  END

HEADER    PROTEIN                                 07-JAN-16   NONE
TITLE     NULL                                                        
COMPND    MOLECULE: Muurolene-alpha                                   
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-JAN-16         0                                  
HETATM    1  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   11                                                  
CONECT    5    4    6    8                                                  
CONECT    6    5    7                                                       
CONECT    7    6    2                                                       
CONECT    8    5    9   15                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10    4   12                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15    8                                                            
MASTER        0    0    0    0    0    0    0    0   15    0   32    0
END

COMPND    HMDB0037784
HETATM    1  C1  UNL     1       3.131  -2.367   0.368  1.00  0.00           C  
HETATM    2  C2  UNL     1       2.186  -1.310   0.005  1.00  0.00           C  
HETATM    3  C3  UNL     1       0.889  -1.323   0.311  1.00  0.00           C  
HETATM    4  C4  UNL     1       0.136  -0.158  -0.155  1.00  0.00           C  
HETATM    5  C5  UNL     1       0.818   1.100   0.348  1.00  0.00           C  
HETATM    6  C6  UNL     1       2.279   1.099   0.080  1.00  0.00           C  
HETATM    7  C7  UNL     1       2.673  -0.123  -0.758  1.00  0.00           C  
HETATM    8  C8  UNL     1       0.103   2.242  -0.299  1.00  0.00           C  
HETATM    9  C9  UNL     1       0.862   3.519  -0.448  1.00  0.00           C  
HETATM   10  C10 UNL     1      -1.151   2.146  -0.729  1.00  0.00           C  
HETATM   11  C11 UNL     1      -1.970   0.919  -0.619  1.00  0.00           C  
HETATM   12  C12 UNL     1      -1.281  -0.084   0.285  1.00  0.00           C  
HETATM   13  C13 UNL     1      -2.012  -1.397   0.256  1.00  0.00           C  
HETATM   14  C14 UNL     1      -2.044  -1.983  -1.141  1.00  0.00           C  
HETATM   15  C15 UNL     1      -3.471  -1.075   0.608  1.00  0.00           C  
HETATM   16  H1  UNL     1       3.387  -3.007  -0.518  1.00  0.00           H  
HETATM   17  H2  UNL     1       4.104  -1.871   0.643  1.00  0.00           H  
HETATM   18  H3  UNL     1       2.842  -3.002   1.200  1.00  0.00           H  
HETATM   19  H4  UNL     1       0.486  -2.164   0.866  1.00  0.00           H  
HETATM   20  H5  UNL     1       0.156  -0.132  -1.271  1.00  0.00           H  
HETATM   21  H6  UNL     1       0.572   1.183   1.446  1.00  0.00           H  
HETATM   22  H7  UNL     1       2.688   2.027  -0.321  1.00  0.00           H  
HETATM   23  H8  UNL     1       2.799   0.934   1.069  1.00  0.00           H  
HETATM   24  H9  UNL     1       3.764  -0.103  -0.869  1.00  0.00           H  
HETATM   25  H10 UNL     1       2.222  -0.059  -1.772  1.00  0.00           H  
HETATM   26  H11 UNL     1       0.155   4.365  -0.593  1.00  0.00           H  
HETATM   27  H12 UNL     1       1.583   3.457  -1.267  1.00  0.00           H  
HETATM   28  H13 UNL     1       1.387   3.672   0.534  1.00  0.00           H  
HETATM   29  H14 UNL     1      -1.572   3.038  -1.183  1.00  0.00           H  
HETATM   30  H15 UNL     1      -2.014   0.457  -1.647  1.00  0.00           H  
HETATM   31  H16 UNL     1      -2.977   1.110  -0.208  1.00  0.00           H  
HETATM   32  H17 UNL     1      -1.350   0.321   1.317  1.00  0.00           H  
HETATM   33  H18 UNL     1      -1.590  -2.127   0.943  1.00  0.00           H  
HETATM   34  H19 UNL     1      -2.867  -1.504  -1.707  1.00  0.00           H  
HETATM   35  H20 UNL     1      -2.356  -3.055  -1.018  1.00  0.00           H  
HETATM   36  H21 UNL     1      -1.071  -1.892  -1.629  1.00  0.00           H  
HETATM   37  H22 UNL     1      -4.000  -0.738  -0.320  1.00  0.00           H  
HETATM   38  H23 UNL     1      -3.526  -0.204   1.305  1.00  0.00           H  
HETATM   39  H24 UNL     1      -3.969  -1.912   1.105  1.00  0.00           H  
CONECT    1    2   16   17   18
CONECT    2    3    3    7
CONECT    3    4   19
CONECT    4    5   12   20
CONECT    5    6    8   21
CONECT    6    7   22   23
CONECT    7   24   25
CONECT    8    9   10   10
CONECT    9   26   27   28
CONECT   10   11   29
CONECT   11   12   30   31
CONECT   12   13   32
CONECT   13   14   15   33
CONECT   14   34   35   36
CONECT   15   37   38   39
END

HMDB0037784
     RDKit          3D
(+)-alpha-Muurolene
 39 40  0  0  0  0  0  0  0  0999 V2000
    3.1313   -2.3670    0.3680 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1859   -1.3096    0.0053 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8890   -1.3230    0.3112 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1363   -0.1580   -0.1549 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8177    1.1003    0.3477 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2792    1.0985    0.0800 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6733   -0.1235   -0.7580 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1025    2.2419   -0.2990 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8617    3.5191   -0.4478 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1510    2.1456   -0.7286 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9698    0.9193   -0.6188 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2811   -0.0838    0.2848 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0119   -1.3974    0.2561 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0436   -1.9826   -1.1408 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4708   -1.0753    0.6082 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3869   -3.0067   -0.5182 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1040   -1.8707    0.6427 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8420   -3.0018    1.2004 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4864   -2.1643    0.8658 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1556   -0.1319   -1.2711 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5724    1.1827    1.4463 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6883    2.0270   -0.3207 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7990    0.9337    1.0694 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7644   -0.1028   -0.8692 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2216   -0.0594   -1.7717 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1548    4.3648   -0.5933 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5828    3.4569   -1.2670 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3865    3.6720    0.5339 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5716    3.0379   -1.1831 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0144    0.4569   -1.6468 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9773    1.1101   -0.2077 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3503    0.3215    1.3166 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5898   -2.1265    0.9429 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8673   -1.5038   -1.7070 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3564   -3.0549   -1.0183 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0712   -1.8917   -1.6290 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9998   -0.7380   -0.3200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5261   -0.2036    1.3048 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9692   -1.9117    1.1048 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  5  8  1  0
  8  9  1  0
  8 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
  7  2  1  0
 12  4  1  0
  1 16  1  0
  1 17  1  0
  1 18  1  0
  3 19  1  0
  4 20  1  0
  5 21  1  0
  6 22  1  0
  6 23  1  0
  7 24  1  0
  7 25  1  0
  9 26  1  0
  9 27  1  0
  9 28  1  0
 10 29  1  0
 11 30  1  0
 11 31  1  0
 12 32  1  0
 13 33  1  0
 14 34  1  0
 14 35  1  0
 14 36  1  0
 15 37  1  0
 15 38  1  0
 15 39  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
(+)-a-Muurolene	Generator
(+)-Α-muurolene	Generator

Chemical Formula

C₁₅H₂₄

Average Molecular Weight

204.357

Monoisotopic Molecular Weight

204.187800773

IUPAC Name

4,7-dimethyl-1-(propan-2-yl)-1,2,4a,5,6,8a-hexahydronaphthalene

Traditional Name

cadinene

CAS Registry Number

17627-24-6

SMILES

CC(C)C1CC=C(C)C2CCC(C)=CC12

InChI Identifier

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

InChI Key

QMAYBMKBYCGXDH-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
Cadinane 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

a sesquiterpenoid (CPD-8799 )

Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Saliva (PMID: 24421258)

Cellular substructure

Membrane (HMDB: HMDB0037784)

Source

Exogenous

Exogenous (HMDB: HMDB0037784)

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	Not Available	Not Available
Water Solubility	0.063 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	0.01 g/L	ALOGPS
logP	5	ALOGPS
logP	4.45	ChemAxon
logS	-4.3	ALOGPS
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	0	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	0 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	68.6 m³·mol⁻¹	ChemAxon
Polarizability	26.35 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]+	150.679	31661259
DarkChem	[M-H]-	147.412	31661259
DeepCCS	[M-2H]-	184.341	30932474
DeepCCS	[M+Na]+	159.891	30932474
AllCCS	[M+H]+	146.8	32859911
AllCCS	[M+H-H2O]+	142.8	32859911
AllCCS	[M+NH4]+	150.5	32859911
AllCCS	[M+Na]+	151.6	32859911
AllCCS	[M-H]-	156.7	32859911
AllCCS	[M+Na-2H]-	157.3	32859911
AllCCS	[M+HCOO]-	158.1	32859911

Predicted Retention Times

Underivatized

Chromatographic Method	Retention Time	Reference
Measured using a Waters Acquity ultraperformance liquid chromatography (UPLC) ethylene-bridged hybrid (BEH) C18 column (100 mm × 2.1 mm; 1.7 μmparticle diameter). Predicted by Afia on May 17, 2022. Predicted by Afia on May 17, 2022.	7.5 minutes	32390414
Predicted by Siyang on May 30, 2022	20.0898 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	1.77 minutes	32390414
AjsUoB = Accucore 150 Amide HILIC with 10mM Ammonium Formate, 0.1% Formic Acid	27.2 seconds	40023050
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	2704.5 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	724.6 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	259.1 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	402.8 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	253.8 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	793.8 seconds	40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid	863.2 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	110.5 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	1610.1 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	588.5 seconds	40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid	1478.4 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	555.2 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	448.1 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	445.5 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	666.1 seconds	40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water	8.3 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
(+)-alpha-Muurolene	CC(C)C1CC=C(C)C2CCC(C)=CC12	1730.4	Standard polar	33892256
(+)-alpha-Muurolene	CC(C)C1CC=C(C)C2CCC(C)=CC12	1492.4	Standard non polar	33892256
(+)-alpha-Muurolene	CC(C)C1CC=C(C)C2CCC(C)=CC12	1486.2	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 - (+)-alpha-Muurolene GC-MS (Non-derivatized) - 70eV, Positive	splash10-01p5-2900000000-6a89474b0f48b85df7ac	2017-07-27	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (+)-alpha-Muurolene 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 - (+)-alpha-Muurolene 10V, Positive-QTOF	splash10-0a4i-1490000000-0ddd4dc1b8a7ab9349f3	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (+)-alpha-Muurolene 20V, Positive-QTOF	splash10-0bta-2920000000-165de06bf400af0ddb4a	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (+)-alpha-Muurolene 40V, Positive-QTOF	splash10-0gvk-6900000000-5ff9ff55cf9f99b37621	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (+)-alpha-Muurolene 10V, Negative-QTOF	splash10-0udi-0090000000-4ae77807dfc4cdd99544	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (+)-alpha-Muurolene 20V, Negative-QTOF	splash10-0udi-0190000000-06ab3445bbd33bd64f05	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (+)-alpha-Muurolene 40V, Negative-QTOF	splash10-0h2s-1910000000-2e79eeb9fcbaa848c4c2	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (+)-alpha-Muurolene 10V, Negative-QTOF	splash10-0udi-0090000000-7ccf03fa1149a1e9f55f	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (+)-alpha-Muurolene 20V, Negative-QTOF	splash10-0udi-0090000000-7ccf03fa1149a1e9f55f	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (+)-alpha-Muurolene 40V, Negative-QTOF	splash10-0pbd-0920000000-11dae2aa0da51f3d364e	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (+)-alpha-Muurolene 10V, Positive-QTOF	splash10-0a4i-1390000000-47f45e86d00ca88bcf52	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (+)-alpha-Muurolene 20V, Positive-QTOF	splash10-052e-9530000000-e6f3c717152a0f0462d1	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (+)-alpha-Muurolene 40V, Positive-QTOF	splash10-0006-9300000000-a7c1fe09f1157fe92f19	2021-09-25	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Membrane

Biospecimen Locations

Saliva

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Saliva	Detected but not Quantified	Not Quantified	Adult (>18 years old)	Not Specified	Normal	24421258	details

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

FDB016927

KNApSAcK ID

C00057150

Chemspider ID

91896

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

101708

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

rw1696991

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 (+)-alpha-Muurolene (HMDB0037784)

MOL for HMDB0037784 ((+)-alpha-Muurolene)

3D MOL for HMDB0037784 ((+)-alpha-Muurolene)

3D SDF for HMDB0037784 ((+)-alpha-Muurolene)

3D-SDF for HMDB0037784 ((+)-alpha-Muurolene)

PDB for HMDB0037784 ((+)-alpha-Muurolene)

3D PDB for HMDB0037784 ((+)-alpha-Muurolene)

SMILES for HMDB0037784 ((+)-alpha-Muurolene)

INCHI for HMDB0037784 ((+)-alpha-Muurolene)

Structure for HMDB0037784 ((+)-alpha-Muurolene)

3D Structure for HMDB0037784 ((+)-alpha-Muurolene)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

GC-MS Spectra

MS/MS Spectra