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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 21:58:29 UTC

Update Date

2022-03-07 02:55:04 UTC

HMDB ID

HMDB0036798

Secondary Accession Numbers

HMDB36798

Metabolite Identification

Common Name

8alpha-3-Copaen-8-ol

Description

8alpha-3-Copaen-8-ol belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. 8alpha-3-Copaen-8-ol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

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

HMDB0036798
     RDKit          3D
8alpha-3-Copaen-8-ol
 40 42  0  0  0  0  0  0  0  0999 V2000
   -3.5096    1.4362   -0.7284 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4632    0.7434    0.0370 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5525    0.6071    1.3467 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4721   -0.1678    2.0558 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3956   -0.5600    1.1009 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0930    0.6553    0.2181 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1671    0.4886   -0.5654 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3367    1.2338    0.0047 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6746    0.8052    1.3947 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5210    1.0131   -0.8904 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4639   -0.9748   -0.7359 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2193   -1.1068   -1.9092 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1990   -1.7785   -0.9385 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9396   -1.2109   -0.1474 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0811   -2.1439    0.0278 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2824    0.1802   -0.6383 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0511    2.2067   -0.1432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0910    1.9892   -1.6168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2664    0.7287   -1.1460 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3635    1.0227    1.9484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0141    0.4749    2.8485 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9563   -1.0174    2.5504 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5122   -0.9907    1.5152 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2594    1.6115    0.7206 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9680    0.8923   -1.5952 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0898    2.3161   -0.0342 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0859   -0.2178    1.3913 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4677    1.5132    1.7695 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8293    0.9275    2.1022 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2694    1.1467   -1.9621 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3216    1.7267   -0.5631 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9434   -0.0032   -0.7376 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9753   -1.3908    0.1460 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6887   -0.6795   -2.6286 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0776   -1.7312   -2.0147 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3911   -2.8363   -0.6199 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9476   -3.0042   -0.6724 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0675   -1.7012   -0.2374 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0714   -2.5640    1.0519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1688    0.3597   -1.7052 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
  7  8  1  0
  8  9  1  0
  8 10  1  0
  7 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
 16  2  1  0
 14  5  1  0
 16  6  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  3 20  1  0
  4 21  1  0
  4 22  1  0
  5 23  1  0
  6 24  1  0
  7 25  1  0
  8 26  1  0
  9 27  1  0
  9 28  1  0
  9 29  1  0
 10 30  1  0
 10 31  1  0
 10 32  1  0
 11 33  1  0
 12 34  1  0
 13 35  1  0
 13 36  1  0
 15 37  1  0
 15 38  1  0
 15 39  1  0
 16 40  1  0
M  END


  Mrv0541 02241218112D          

 16 18  0  0  0  0            999 V2000
    1.2005    0.0671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4002   -0.2002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4667    0.3333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2000    0.2668    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3331    1.0671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1340    0.9340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8011    1.4010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7340    1.8680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4667    1.0671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2010    0.6667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1340   -0.2002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4002   -0.4670    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8011   -0.6672    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6004   -1.8680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0668   -1.2008    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7335   -1.4010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  6  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3  9  1  0  0  0  0
  4  5  1  0  0  0  0
  4 12  1  0  0  0  0
  5  6  1  0  0  0  0
  5  9  1  0  0  0  0
  6  7  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 12 15  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0036798

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(C)C1C2C3CC=C(C)C2C3(C)CC1O

> <INCHI_IDENTIFIER>
InChI=1S/C15H24O/c1-8(2)12-11(16)7-15(4)10-6-5-9(3)14(15)13(10)12/h5,8,10-14,16H,6-7H2,1-4H3

> <INCHI_KEY>
BVCNHEVITXGCEP-UHFFFAOYSA-N

> <FORMULA>
C15H24O

> <MOLECULAR_WEIGHT>
220.3505

> <EXACT_MASS>
220.18271539

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_AVERAGE_POLARIZABILITY>
26.87824219917133

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2,8-dimethyl-5-(propan-2-yl)tricyclo[4.4.0.0²,⁷]dec-8-en-4-ol

> <ALOGPS_LOGP>
2.50

> <JCHEM_LOGP>
2.7793653656666675

> <ALOGPS_LOGS>
-2.92

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
19.761077477857274

> <JCHEM_PKA_STRONGEST_BASIC>
-0.7163047111852271

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
67.3604

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.66e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-isopropyl-2,8-dimethyltricyclo[4.4.0.0²,⁷]dec-8-en-4-ol

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0036798
     RDKit          3D
8alpha-3-Copaen-8-ol
 40 42  0  0  0  0  0  0  0  0999 V2000
   -3.5096    1.4362   -0.7284 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4632    0.7434    0.0370 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5525    0.6071    1.3467 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4721   -0.1678    2.0558 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3956   -0.5600    1.1009 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0930    0.6553    0.2181 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1671    0.4886   -0.5654 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3367    1.2338    0.0047 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6746    0.8052    1.3947 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5210    1.0131   -0.8904 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4639   -0.9748   -0.7359 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2193   -1.1068   -1.9092 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1990   -1.7785   -0.9385 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9396   -1.2109   -0.1474 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0811   -2.1439    0.0278 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2824    0.1802   -0.6383 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0511    2.2067   -0.1432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0910    1.9892   -1.6168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2664    0.7287   -1.1460 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3635    1.0227    1.9484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0141    0.4749    2.8485 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9563   -1.0174    2.5504 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5122   -0.9907    1.5152 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2594    1.6115    0.7206 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9680    0.8923   -1.5952 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0898    2.3161   -0.0342 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0859   -0.2178    1.3913 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4677    1.5132    1.7695 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8293    0.9275    2.1022 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2694    1.1467   -1.9621 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3216    1.7267   -0.5631 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9434   -0.0032   -0.7376 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9753   -1.3908    0.1460 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6887   -0.6795   -2.6286 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0776   -1.7312   -2.0147 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3911   -2.8363   -0.6199 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9476   -3.0042   -0.6724 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0675   -1.7012   -0.2374 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0714   -2.5640    1.0519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1688    0.3597   -1.7052 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
  7  8  1  0
  8  9  1  0
  8 10  1  0
  7 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
 16  2  1  0
 14  5  1  0
 16  6  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  3 20  1  0
  4 21  1  0
  4 22  1  0
  5 23  1  0
  6 24  1  0
  7 25  1  0
  8 26  1  0
  9 27  1  0
  9 28  1  0
  9 29  1  0
 10 30  1  0
 10 31  1  0
 10 32  1  0
 11 33  1  0
 12 34  1  0
 13 35  1  0
 13 36  1  0
 15 37  1  0
 15 38  1  0
 15 39  1  0
 16 40  1  0
M  END

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0       2.241   0.125   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.747  -0.374   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.871   0.622   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.373   0.498   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.622   1.992   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.117   1.743   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.362   2.615   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.370   3.487   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.871   1.992   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.242   1.245   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.117  -0.374   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.747  -0.872   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -3.362  -1.245   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -1.121  -3.487   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.125  -2.241   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.369  -2.615   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4    9                                                  
CONECT    4    3    5   12                                                  
CONECT    5    4    6    9                                                  
CONECT    6    1    5    7                                                  
CONECT    7    6                                                            
CONECT    8    9                                                            
CONECT    9    3    5    8   10                                             
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12    4   11   15                                                  
CONECT   13   11                                                            
CONECT   14   15                                                            
CONECT   15   12   14   16                                                  
CONECT   16   15                                                            
MASTER        0    0    0    0    0    0    0    0   16    0   36    0
END

COMPND    HMDB0036798
HETATM    1  C1  UNL     1      -3.510   1.436  -0.728  1.00  0.00           C  
HETATM    2  C2  UNL     1      -2.463   0.743   0.037  1.00  0.00           C  
HETATM    3  C3  UNL     1      -2.552   0.607   1.347  1.00  0.00           C  
HETATM    4  C4  UNL     1      -1.472  -0.168   2.056  1.00  0.00           C  
HETATM    5  C5  UNL     1      -0.396  -0.560   1.101  1.00  0.00           C  
HETATM    6  C6  UNL     1      -0.093   0.655   0.218  1.00  0.00           C  
HETATM    7  C7  UNL     1       1.167   0.489  -0.565  1.00  0.00           C  
HETATM    8  C8  UNL     1       2.337   1.234   0.005  1.00  0.00           C  
HETATM    9  C9  UNL     1       2.675   0.805   1.395  1.00  0.00           C  
HETATM   10  C10 UNL     1       3.521   1.013  -0.890  1.00  0.00           C  
HETATM   11  C11 UNL     1       1.464  -0.975  -0.736  1.00  0.00           C  
HETATM   12  O1  UNL     1       2.219  -1.107  -1.909  1.00  0.00           O  
HETATM   13  C12 UNL     1       0.199  -1.778  -0.938  1.00  0.00           C  
HETATM   14  C13 UNL     1      -0.940  -1.211  -0.147  1.00  0.00           C  
HETATM   15  C14 UNL     1      -2.081  -2.144   0.028  1.00  0.00           C  
HETATM   16  C15 UNL     1      -1.282   0.180  -0.638  1.00  0.00           C  
HETATM   17  H1  UNL     1      -4.051   2.207  -0.143  1.00  0.00           H  
HETATM   18  H2  UNL     1      -3.091   1.989  -1.617  1.00  0.00           H  
HETATM   19  H3  UNL     1      -4.266   0.729  -1.146  1.00  0.00           H  
HETATM   20  H4  UNL     1      -3.364   1.023   1.948  1.00  0.00           H  
HETATM   21  H5  UNL     1      -1.014   0.475   2.849  1.00  0.00           H  
HETATM   22  H6  UNL     1      -1.956  -1.017   2.550  1.00  0.00           H  
HETATM   23  H7  UNL     1       0.512  -0.991   1.515  1.00  0.00           H  
HETATM   24  H8  UNL     1      -0.259   1.612   0.721  1.00  0.00           H  
HETATM   25  H9  UNL     1       0.968   0.892  -1.595  1.00  0.00           H  
HETATM   26  H10 UNL     1       2.090   2.316  -0.034  1.00  0.00           H  
HETATM   27  H11 UNL     1       3.086  -0.218   1.391  1.00  0.00           H  
HETATM   28  H12 UNL     1       3.468   1.513   1.770  1.00  0.00           H  
HETATM   29  H13 UNL     1       1.829   0.927   2.102  1.00  0.00           H  
HETATM   30  H14 UNL     1       3.269   1.147  -1.962  1.00  0.00           H  
HETATM   31  H15 UNL     1       4.322   1.727  -0.563  1.00  0.00           H  
HETATM   32  H16 UNL     1       3.943  -0.003  -0.738  1.00  0.00           H  
HETATM   33  H17 UNL     1       1.975  -1.391   0.146  1.00  0.00           H  
HETATM   34  H18 UNL     1       1.689  -0.680  -2.629  1.00  0.00           H  
HETATM   35  H19 UNL     1      -0.078  -1.731  -2.015  1.00  0.00           H  
HETATM   36  H20 UNL     1       0.391  -2.836  -0.620  1.00  0.00           H  
HETATM   37  H21 UNL     1      -1.948  -3.004  -0.672  1.00  0.00           H  
HETATM   38  H22 UNL     1      -3.067  -1.701  -0.237  1.00  0.00           H  
HETATM   39  H23 UNL     1      -2.071  -2.564   1.052  1.00  0.00           H  
HETATM   40  H24 UNL     1      -1.169   0.360  -1.705  1.00  0.00           H  
CONECT    1    2   17   18   19
CONECT    2    3    3   16
CONECT    3    4   20
CONECT    4    5   21   22
CONECT    5    6   14   23
CONECT    6    7   16   24
CONECT    7    8   11   25
CONECT    8    9   10   26
CONECT    9   27   28   29
CONECT   10   30   31   32
CONECT   11   12   13   33
CONECT   12   34
CONECT   13   14   35   36
CONECT   14   15   16
CONECT   15   37   38   39
CONECT   16   40
END

HMDB0036798
     RDKit          3D
8alpha-3-Copaen-8-ol
 40 42  0  0  0  0  0  0  0  0999 V2000
   -3.5096    1.4362   -0.7284 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4632    0.7434    0.0370 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5525    0.6071    1.3467 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4721   -0.1678    2.0558 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3956   -0.5600    1.1009 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0930    0.6553    0.2181 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1671    0.4886   -0.5654 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3367    1.2338    0.0047 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6746    0.8052    1.3947 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5210    1.0131   -0.8904 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4639   -0.9748   -0.7359 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2193   -1.1068   -1.9092 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1990   -1.7785   -0.9385 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9396   -1.2109   -0.1474 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0811   -2.1439    0.0278 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2824    0.1802   -0.6383 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0511    2.2067   -0.1432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0910    1.9892   -1.6168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2664    0.7287   -1.1460 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3635    1.0227    1.9484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0141    0.4749    2.8485 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9563   -1.0174    2.5504 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5122   -0.9907    1.5152 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2594    1.6115    0.7206 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9680    0.8923   -1.5952 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0898    2.3161   -0.0342 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0859   -0.2178    1.3913 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4677    1.5132    1.7695 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8293    0.9275    2.1022 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2694    1.1467   -1.9621 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3216    1.7267   -0.5631 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9434   -0.0032   -0.7376 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9753   -1.3908    0.1460 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6887   -0.6795   -2.6286 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0776   -1.7312   -2.0147 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3911   -2.8363   -0.6199 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9476   -3.0042   -0.6724 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0675   -1.7012   -0.2374 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0714   -2.5640    1.0519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1688    0.3597   -1.7052 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
  7  8  1  0
  8  9  1  0
  8 10  1  0
  7 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
 16  2  1  0
 14  5  1  0
 16  6  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  3 20  1  0
  4 21  1  0
  4 22  1  0
  5 23  1  0
  6 24  1  0
  7 25  1  0
  8 26  1  0
  9 27  1  0
  9 28  1  0
  9 29  1  0
 10 30  1  0
 10 31  1  0
 10 32  1  0
 11 33  1  0
 12 34  1  0
 13 35  1  0
 13 36  1  0
 15 37  1  0
 15 38  1  0
 15 39  1  0
 16 40  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
8a-3-Copaen-8-ol	Generator
8Α-3-copaen-8-ol	Generator
alpha-Copaen-8-ol	HMDB

Chemical Formula

C₁₅H₂₄O

Average Molecular Weight

220.3505

Monoisotopic Molecular Weight

220.18271539

IUPAC Name

2,8-dimethyl-5-(propan-2-yl)tricyclo[4.4.0.0²,⁷]dec-8-en-4-ol

Traditional Name

5-isopropyl-2,8-dimethyltricyclo[4.4.0.0²,⁷]dec-8-en-4-ol

CAS Registry Number

58569-25-8

SMILES

CC(C)C1C2C3CC=C(C)C2C3(C)CC1O

InChI Identifier

InChI=1S/C15H24O/c1-8(2)12-11(16)7-15(4)10-6-5-9(3)14(15)13(10)12/h5,8,10-14,16H,6-7H2,1-4H3

InChI Key

BVCNHEVITXGCEP-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

Copaane sesquiterpenoid
Sesquiterpenoid
Cyclic alcohol
Secondary alcohol
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cell membrane (HMDB: HMDB0036798)

Cellular substructure

Route of exposure

Enteral

Ingestion (HMDB: HMDB0036798)

Source

Endogenous

Endogenous (HMDB: HMDB0036798)

Plant

Plant (HMDB: HMDB0036798)

Animal

Animal (HMDB: HMDB0036798)

Exogenous

Food

Food (HMDB: HMDB0036798)

Herb and spice

Herbs and Spices (FooDB: FOOD00866)

Vegetable

Leaf vegetable

Green vegetables (FooDB: FOOD00872)

Fat and oil

Fats and oils (FooDB: FOOD00864)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid peroxidation (HMDB: HMDB0036798)

Biochemical process

Fatty acid metabolism (HMDB: HMDB0036798)

Cellular process

Cell signaling (HMDB: HMDB0036798)

Biochemical pathway

Lipid metabolism pathway (HMDB: HMDB0036798)

Role

Biological role

Membrane stabilizer (HMDB: HMDB0036798)

Nutrient

Nutrient (HMDB: HMDB0036798)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0036798)

Emulsifier (HMDB: HMDB0036798)

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	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.27 g/L	ALOGPS
logP	2.5	ALOGPS
logP	2.78	ChemAxon
logS	-2.9	ALOGPS
pKa (Strongest Acidic)	19.76	ChemAxon
pKa (Strongest Basic)	-0.72	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	20.23 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	67.36 m³·mol⁻¹	ChemAxon
Polarizability	26.88 Å³	ChemAxon
Number of Rings	3	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]+	150.063	31661259
DarkChem	[M-H]-	148.739	31661259
DeepCCS	[M+H]+	155.374	30932474
DeepCCS	[M-H]-	153.016	30932474
DeepCCS	[M-2H]-	186.875	30932474
DeepCCS	[M+Na]+	161.843	30932474
AllCCS	[M+H]+	151.5	32859911
AllCCS	[M+H-H2O]+	147.8	32859911
AllCCS	[M+NH4]+	155.0	32859911
AllCCS	[M+Na]+	156.0	32859911
AllCCS	[M-H]-	160.7	32859911
AllCCS	[M+Na-2H]-	161.0	32859911
AllCCS	[M+HCOO]-	161.4	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
8alpha-3-Copaen-8-ol	CC(C)C1C2C3CC=C(C)C2C3(C)CC1O	2205.5	Standard polar	33892256
8alpha-3-Copaen-8-ol	CC(C)C1C2C3CC=C(C)C2C3(C)CC1O	1610.7	Standard non polar	33892256
8alpha-3-Copaen-8-ol	CC(C)C1C2C3CC=C(C)C2C3(C)CC1O	1593.3	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
8alpha-3-Copaen-8-ol,1TMS,isomer #1	CC1=CCC2C3C(C(C)C)C(O[Si](C)(C)C)CC2(C)C13	1693.5	Semi standard non polar	33892256
8alpha-3-Copaen-8-ol,1TBDMS,isomer #1	CC1=CCC2C3C(C(C)C)C(O[Si](C)(C)C(C)(C)C)CC2(C)C13	1987.8	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 - 8alpha-3-Copaen-8-ol GC-MS (Non-derivatized) - 70eV, Positive	splash10-05mo-9840000000-196725926366ea8e6467	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 8alpha-3-Copaen-8-ol GC-MS (1 TMS) - 70eV, Positive	splash10-00bc-9260000000-16e31c201e764d0cd84d	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 8alpha-3-Copaen-8-ol 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 - 8alpha-3-Copaen-8-ol 10V, Positive-QTOF	splash10-0uk9-0090000000-3cbb5f638205cc67e191	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8alpha-3-Copaen-8-ol 20V, Positive-QTOF	splash10-0uk9-0390000000-ecaa0a31e82d297b33be	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8alpha-3-Copaen-8-ol 40V, Positive-QTOF	splash10-0f79-0950000000-16fd9ef19d5c2f28db6a	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8alpha-3-Copaen-8-ol 10V, Negative-QTOF	splash10-014i-0090000000-cebf6f7be23c3fc0ff03	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8alpha-3-Copaen-8-ol 20V, Negative-QTOF	splash10-014i-0090000000-a58063e67bd891590add	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8alpha-3-Copaen-8-ol 40V, Negative-QTOF	splash10-0uxr-0690000000-227ae1ac0961548ff1bf	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8alpha-3-Copaen-8-ol 10V, Positive-QTOF	splash10-00di-0890000000-06fd1b16280007f167a3	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8alpha-3-Copaen-8-ol 20V, Positive-QTOF	splash10-00di-1920000000-817443c15b2e0af1e27c	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8alpha-3-Copaen-8-ol 40V, Positive-QTOF	splash10-001i-9110000000-74962ec252945d1b9328	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8alpha-3-Copaen-8-ol 10V, Negative-QTOF	splash10-014i-0090000000-4af4c4ee1c4acef7e18b	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8alpha-3-Copaen-8-ol 20V, Negative-QTOF	splash10-014i-0090000000-4af4c4ee1c4acef7e18b	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8alpha-3-Copaen-8-ol 40V, Negative-QTOF	splash10-0gba-0690000000-4997ef99985457b53daf	2021-09-23	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Cytoplasm
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

FDB015744

KNApSAcK ID

C00021868

Chemspider ID

501776

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

577203

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

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 8alpha-3-Copaen-8-ol (HMDB0036798)

MOL for HMDB0036798 (8alpha-3-Copaen-8-ol)

3D MOL for HMDB0036798 (8alpha-3-Copaen-8-ol)

3D SDF for HMDB0036798 (8alpha-3-Copaen-8-ol)

3D-SDF for HMDB0036798 (8alpha-3-Copaen-8-ol)

PDB for HMDB0036798 (8alpha-3-Copaen-8-ol)

3D PDB for HMDB0036798 (8alpha-3-Copaen-8-ol)

SMILES for HMDB0036798 (8alpha-3-Copaen-8-ol)

INCHI for HMDB0036798 (8alpha-3-Copaen-8-ol)

Structure for HMDB0036798 (8alpha-3-Copaen-8-ol)

3D Structure for HMDB0036798 (8alpha-3-Copaen-8-ol)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra