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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 21:58:12 UTC

Update Date

2022-03-07 02:55:03 UTC

HMDB ID

HMDB0036793

Secondary Accession Numbers

HMDB36793

Metabolite Identification

Common Name

3,15-Epoxy-6-caryophyllene

Description

3,15-Epoxy-6-caryophyllene belongs to the class of organic compounds known as epoxides. Epoxides are compounds containing a cyclic ether with three ring atoms(one oxygen and two carbon atoms). 3,15-Epoxy-6-caryophyllene has been detected, but not quantified in, herbs and spices. This could make 3,15-epoxy-6-caryophyllene a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on 3,15-Epoxy-6-caryophyllene.

Structure

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

HMDB0036793
     RDKit          3D
3,15-Epoxy-6-caryophyllene
 40 42  0  0  0  0  0  0  0  0999 V2000
    2.5430   -2.1690   -1.3624 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2559   -1.0388   -0.4472 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5796    0.1734   -0.8220 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3502    1.3938   -0.0070 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1834    2.1523   -0.5734 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0487    1.9690    0.2474 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7163    3.2935    0.6421 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1406    2.4193    1.5317 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9518    0.9845   -0.3575 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1540    0.5432    0.4205 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9504   -0.8308   -0.2356 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6219   -0.8422   -1.5812 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2685   -1.9959    0.6364 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4605   -0.4529   -0.2894 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2269   -0.7851    0.9829 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6246   -1.2911    0.8423 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5256   -2.6616   -1.1022 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7890   -2.9783   -1.2884 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6734   -1.8330   -2.4266 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0468    0.3177   -1.7875 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2355    1.1877    1.0690 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2528    2.0314   -0.1137 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9606    1.7747   -1.6119 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4468    3.2380   -0.7391 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8191    3.3611    0.5565 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1555    4.2289    0.4870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2363    1.2397   -1.3963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0137    0.5152    1.5256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1215    0.9751    0.1418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5446   -1.4781   -1.4927 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0109   -1.2679   -2.3811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0160    0.1712   -1.8722 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5753   -2.8482    0.4870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3979   -1.6941    1.6796 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2759   -2.3864    0.3051 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0255   -0.7980   -1.2177 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1773    0.1079    1.6664 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3680   -1.5715    1.5227 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6991   -2.3796    1.1303 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2511   -0.7749    1.6288 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
  6  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 11 13  1  0
 11 14  1  0
 14 15  1  0
 15 16  1  0
 16  2  1  0
  8  6  1  0
 14  9  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
  5 24  1  0
  7 25  1  0
  7 26  1  0
  9 27  1  0
 10 28  1  0
 10 29  1  0
 12 30  1  0
 12 31  1  0
 12 32  1  0
 13 33  1  0
 13 34  1  0
 13 35  1  0
 14 36  1  0
 15 37  1  0
 15 38  1  0
 16 39  1  0
 16 40  1  0
M  END

  Mrv0541 05061309202D          

 16 18  0  0  0  0            999 V2000
    3.8831    1.1748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9401    4.4862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0671    4.1842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7651    0.6817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5776    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1079    2.2820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5776    2.9140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0506    1.0942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6381    3.3592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0540    1.4570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1079    1.4570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7651    3.0572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0506    2.6447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3526    3.7717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7685    1.8695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0540    2.2820    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  5  4  1  0  0  0  0
  7  6  1  0  0  0  0
  8  4  1  0  0  0  0
 11  1  1  0  0  0  0
 11  5  2  0  0  0  0
 11  6  1  0  0  0  0
 12  7  1  0  0  0  0
 13  9  1  0  0  0  0
 13 12  1  0  0  0  0
 14  2  1  0  0  0  0
 14  3  1  0  0  0  0
 14  9  1  0  0  0  0
 14 12  1  0  0  0  0
 15  8  1  0  0  0  0
 15 10  1  0  0  0  0
 15 13  1  0  0  0  0
 16 10  1  0  0  0  0
 16 15  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0036793

> <DATABASE_NAME>
hmdb

> <SMILES>
C\C1=C\CCC2(CO2)C2CC(C)(C)C2CC1

> <INCHI_IDENTIFIER>
InChI=1S/C15H24O/c1-11-5-4-8-15(10-16-15)13-9-14(2,3)12(13)7-6-11/h5,12-13H,4,6-10H2,1-3H3/b11-5-

> <INCHI_KEY>
AURKDPLYMRHYAY-WZUFQYTHSA-N

> <FORMULA>
C15H24O

> <MOLECULAR_WEIGHT>
220.3505

> <EXACT_MASS>
220.18271539

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_AVERAGE_POLARIZABILITY>
26.975374364479467

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(5Z)-6,10,10-trimethylspiro[bicyclo[7.2.0]undecane-2,2'-oxiran]-5-ene

> <ALOGPS_LOGP>
3.38

> <JCHEM_LOGP>
3.666541583333333

> <ALOGPS_LOGS>
-4.69

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.204694326423602

> <JCHEM_POLAR_SURFACE_AREA>
12.53

> <JCHEM_REFRACTIVITY>
67.3906

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.49e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(5Z)-6,10,10-trimethylspiro[bicyclo[7.2.0]undecane-2,2'-oxiran]-5-ene

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0036793
     RDKit          3D
3,15-Epoxy-6-caryophyllene
 40 42  0  0  0  0  0  0  0  0999 V2000
    2.5430   -2.1690   -1.3624 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2559   -1.0388   -0.4472 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5796    0.1734   -0.8220 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3502    1.3938   -0.0070 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1834    2.1523   -0.5734 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0487    1.9690    0.2474 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7163    3.2935    0.6421 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1406    2.4193    1.5317 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9518    0.9845   -0.3575 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1540    0.5432    0.4205 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9504   -0.8308   -0.2356 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6219   -0.8422   -1.5812 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2685   -1.9959    0.6364 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4605   -0.4529   -0.2894 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2269   -0.7851    0.9829 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6246   -1.2911    0.8423 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5256   -2.6616   -1.1022 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7890   -2.9783   -1.2884 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6734   -1.8330   -2.4266 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0468    0.3177   -1.7875 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2355    1.1877    1.0690 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2528    2.0314   -0.1137 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9606    1.7747   -1.6119 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4468    3.2380   -0.7391 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8191    3.3611    0.5565 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1555    4.2289    0.4870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2363    1.2397   -1.3963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0137    0.5152    1.5256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1215    0.9751    0.1418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5446   -1.4781   -1.4927 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0109   -1.2679   -2.3811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0160    0.1712   -1.8722 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5753   -2.8482    0.4870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3979   -1.6941    1.6796 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2759   -2.3864    0.3051 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0255   -0.7980   -1.2177 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1773    0.1079    1.6664 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3680   -1.5715    1.5227 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6991   -2.3796    1.1303 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2511   -0.7749    1.6288 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
  6  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 11 13  1  0
 11 14  1  0
 14 15  1  0
 15 16  1  0
 16  2  1  0
  8  6  1  0
 14  9  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
  5 24  1  0
  7 25  1  0
  7 26  1  0
  9 27  1  0
 10 28  1  0
 10 29  1  0
 12 30  1  0
 12 31  1  0
 12 32  1  0
 13 33  1  0
 13 34  1  0
 13 35  1  0
 14 36  1  0
 15 37  1  0
 15 38  1  0
 16 39  1  0
 16 40  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       7.248   2.193   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.755   8.374   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.859   7.811   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.295   1.273   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.812   1.540   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.801   4.260   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.812   5.439   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.961   2.043   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.191   6.271   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.101   2.720   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.801   2.720   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.295   5.707   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.961   4.937   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.525   7.041   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.435   3.490   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       0.101   4.260   0.000  0.00  0.00           O+0
CONECT    1   11                                                            
CONECT    2   14                                                            
CONECT    3   14                                                            
CONECT    4    5    8                                                       
CONECT    5    4   11                                                       
CONECT    6    7   11                                                       
CONECT    7    6   12                                                       
CONECT    8    4   15                                                       
CONECT    9   13   14                                                       
CONECT   10   15   16                                                       
CONECT   11    1    5    6                                                  
CONECT   12    7   13   14                                                  
CONECT   13    9   12   15                                                  
CONECT   14    2    3    9   12                                             
CONECT   15    8   10   13   16                                             
CONECT   16   10   15                                                       
MASTER        0    0    0    0    0    0    0    0   16    0   36    0
END

COMPND    HMDB0036793
HETATM    1  C1  UNL     1       2.543  -2.169  -1.362  1.00  0.00           C  
HETATM    2  C2  UNL     1       2.256  -1.039  -0.447  1.00  0.00           C  
HETATM    3  C3  UNL     1       2.580   0.173  -0.822  1.00  0.00           C  
HETATM    4  C4  UNL     1       2.350   1.394  -0.007  1.00  0.00           C  
HETATM    5  C5  UNL     1       1.183   2.152  -0.573  1.00  0.00           C  
HETATM    6  C6  UNL     1      -0.049   1.969   0.247  1.00  0.00           C  
HETATM    7  C7  UNL     1      -0.716   3.293   0.642  1.00  0.00           C  
HETATM    8  O1  UNL     1      -0.141   2.419   1.532  1.00  0.00           O  
HETATM    9  C8  UNL     1      -0.952   0.984  -0.357  1.00  0.00           C  
HETATM   10  C9  UNL     1      -2.154   0.543   0.420  1.00  0.00           C  
HETATM   11  C10 UNL     1      -1.950  -0.831  -0.236  1.00  0.00           C  
HETATM   12  C11 UNL     1      -2.622  -0.842  -1.581  1.00  0.00           C  
HETATM   13  C12 UNL     1      -2.269  -1.996   0.636  1.00  0.00           C  
HETATM   14  C13 UNL     1      -0.461  -0.453  -0.289  1.00  0.00           C  
HETATM   15  C14 UNL     1       0.227  -0.785   0.983  1.00  0.00           C  
HETATM   16  C15 UNL     1       1.625  -1.291   0.842  1.00  0.00           C  
HETATM   17  H1  UNL     1       3.526  -2.662  -1.102  1.00  0.00           H  
HETATM   18  H2  UNL     1       1.789  -2.978  -1.288  1.00  0.00           H  
HETATM   19  H3  UNL     1       2.673  -1.833  -2.427  1.00  0.00           H  
HETATM   20  H4  UNL     1       3.047   0.318  -1.787  1.00  0.00           H  
HETATM   21  H5  UNL     1       2.236   1.188   1.069  1.00  0.00           H  
HETATM   22  H6  UNL     1       3.253   2.031  -0.114  1.00  0.00           H  
HETATM   23  H7  UNL     1       0.961   1.775  -1.612  1.00  0.00           H  
HETATM   24  H8  UNL     1       1.447   3.238  -0.739  1.00  0.00           H  
HETATM   25  H9  UNL     1      -1.819   3.361   0.556  1.00  0.00           H  
HETATM   26  H10 UNL     1      -0.156   4.229   0.487  1.00  0.00           H  
HETATM   27  H11 UNL     1      -1.236   1.240  -1.396  1.00  0.00           H  
HETATM   28  H12 UNL     1      -2.014   0.515   1.526  1.00  0.00           H  
HETATM   29  H13 UNL     1      -3.122   0.975   0.142  1.00  0.00           H  
HETATM   30  H14 UNL     1      -3.545  -1.478  -1.493  1.00  0.00           H  
HETATM   31  H15 UNL     1      -2.011  -1.268  -2.381  1.00  0.00           H  
HETATM   32  H16 UNL     1      -3.016   0.171  -1.872  1.00  0.00           H  
HETATM   33  H17 UNL     1      -1.575  -2.848   0.487  1.00  0.00           H  
HETATM   34  H18 UNL     1      -2.398  -1.694   1.680  1.00  0.00           H  
HETATM   35  H19 UNL     1      -3.276  -2.386   0.305  1.00  0.00           H  
HETATM   36  H20 UNL     1       0.026  -0.798  -1.218  1.00  0.00           H  
HETATM   37  H21 UNL     1       0.177   0.108   1.666  1.00  0.00           H  
HETATM   38  H22 UNL     1      -0.368  -1.572   1.523  1.00  0.00           H  
HETATM   39  H23 UNL     1       1.699  -2.380   1.130  1.00  0.00           H  
HETATM   40  H24 UNL     1       2.251  -0.775   1.629  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   23   24
CONECT    6    7    8    9
CONECT    7    8   25   26
CONECT    9   10   14   27
CONECT   10   11   28   29
CONECT   11   12   13   14
CONECT   12   30   31   32
CONECT   13   33   34   35
CONECT   14   15   36
CONECT   15   16   37   38
CONECT   16   39   40
END

HMDB0036793
     RDKit          3D
3,15-Epoxy-6-caryophyllene
 40 42  0  0  0  0  0  0  0  0999 V2000
    2.5430   -2.1690   -1.3624 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2559   -1.0388   -0.4472 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5796    0.1734   -0.8220 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3502    1.3938   -0.0070 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1834    2.1523   -0.5734 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0487    1.9690    0.2474 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7163    3.2935    0.6421 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1406    2.4193    1.5317 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9518    0.9845   -0.3575 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1540    0.5432    0.4205 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9504   -0.8308   -0.2356 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6219   -0.8422   -1.5812 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2685   -1.9959    0.6364 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4605   -0.4529   -0.2894 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2269   -0.7851    0.9829 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6246   -1.2911    0.8423 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5256   -2.6616   -1.1022 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7890   -2.9783   -1.2884 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6734   -1.8330   -2.4266 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0468    0.3177   -1.7875 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2355    1.1877    1.0690 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2528    2.0314   -0.1137 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9606    1.7747   -1.6119 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4468    3.2380   -0.7391 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8191    3.3611    0.5565 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1555    4.2289    0.4870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2363    1.2397   -1.3963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0137    0.5152    1.5256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1215    0.9751    0.1418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5446   -1.4781   -1.4927 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0109   -1.2679   -2.3811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0160    0.1712   -1.8722 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5753   -2.8482    0.4870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3979   -1.6941    1.6796 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2759   -2.3864    0.3051 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0255   -0.7980   -1.2177 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1773    0.1079    1.6664 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3680   -1.5715    1.5227 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6991   -2.3796    1.1303 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2511   -0.7749    1.6288 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
  6  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 11 13  1  0
 11 14  1  0
 14 15  1  0
 15 16  1  0
 16  2  1  0
  8  6  1  0
 14  9  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
  5 24  1  0
  7 25  1  0
  7 26  1  0
  9 27  1  0
 10 28  1  0
 10 29  1  0
 12 30  1  0
 12 31  1  0
 12 32  1  0
 13 33  1  0
 13 34  1  0
 13 35  1  0
 14 36  1  0
 15 37  1  0
 15 38  1  0
 16 39  1  0
 16 40  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
3',15-Epoxy-6-caryophyllene	HMDB
[1S-(1R,2S,5E,9S*)]- 6,10,10-trimethyl-spiro[bicyclo[7.2.0]undec-5-ene-2,2'-oxirane]	HMDB

Chemical Formula

C₁₅H₂₄O

Average Molecular Weight

220.3505

Monoisotopic Molecular Weight

220.18271539

IUPAC Name

(5Z)-6,10,10-trimethylspiro[bicyclo[7.2.0]undecane-2,2'-oxiran]-5-ene

Traditional Name

(5Z)-6,10,10-trimethylspiro[bicyclo[7.2.0]undecane-2,2'-oxiran]-5-ene

CAS Registry Number

88395-50-0

SMILES

C\C1=C\CCC2(CO2)C2CC(C)(C)C2CC1

InChI Identifier

InChI=1S/C15H24O/c1-11-5-4-8-15(10-16-15)13-9-14(2,3)12(13)7-6-11/h5,12-13H,4,6-10H2,1-3H3/b11-5-

InChI Key

AURKDPLYMRHYAY-WZUFQYTHSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as epoxides. Epoxides are compounds containing a cyclic ether with three ring atoms(one oxygen and two carbon atoms).

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Epoxides

Sub Class

Not Available

Direct Parent

Epoxides

Alternative Parents

Substituents

Oxacycle
Ether
Oxirane
Dialkyl ether
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Route of exposure

Enteral

Ingestion (HMDB: HMDB0036793)

Source

Endogenous

Endogenous (HMDB: HMDB0036793)

Plant

Plant (HMDB: HMDB0036793)

Exogenous

Food

Food (HMDB: HMDB0036793)

Herb and spice

Herbs and Spices (FooDB: FOOD00866)

Exogenous (HMDB: HMDB0036793)

Process

Naturally occurring process

Biological process

Cellular process

Cell signaling (HMDB: HMDB0036793)

Role

Biological role

Energy source (HMDB: HMDB0036793)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0036793)

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	2.23 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	0.0045 g/L	ALOGPS
logP	3.38	ALOGPS
logP	3.67	ChemAxon
logS	-4.7	ALOGPS
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	12.53 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	67.39 m³·mol⁻¹	ChemAxon
Polarizability	26.98 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]+	148.693	31661259
DarkChem	[M-H]-	146.055	31661259
DeepCCS	[M+H]+	156.701	30932474
DeepCCS	[M-H]-	154.343	30932474
DeepCCS	[M-2H]-	187.629	30932474
DeepCCS	[M+Na]+	162.795	30932474
AllCCS	[M+H]+	151.2	32859911
AllCCS	[M+H-H2O]+	147.3	32859911
AllCCS	[M+NH4]+	154.8	32859911
AllCCS	[M+Na]+	155.8	32859911
AllCCS	[M-H]-	160.9	32859911
AllCCS	[M+Na-2H]-	161.1	32859911
AllCCS	[M+HCOO]-	161.4	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
3,15-Epoxy-6-caryophyllene	C\C1=C\CCC2(CO2)C2CC(C)(C)C2CC1	2177.2	Standard polar	33892256
3,15-Epoxy-6-caryophyllene	C\C1=C\CCC2(CO2)C2CC(C)(C)C2CC1	1643.0	Standard non polar	33892256
3,15-Epoxy-6-caryophyllene	C\C1=C\CCC2(CO2)C2CC(C)(C)C2CC1	1635.8	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 - 3,15-Epoxy-6-caryophyllene GC-MS (Non-derivatized) - 70eV, Positive	splash10-0bt9-4920000000-ac4503e3023051ab785d	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3,15-Epoxy-6-caryophyllene GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3,15-Epoxy-6-caryophyllene 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 - 3,15-Epoxy-6-caryophyllene 10V, Positive-QTOF	splash10-00di-0290000000-8c84f09826f995fcf4bb	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3,15-Epoxy-6-caryophyllene 20V, Positive-QTOF	splash10-0kmu-2790000000-a6fcd475a0fa87f7834c	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3,15-Epoxy-6-caryophyllene 40V, Positive-QTOF	splash10-05o1-9300000000-369c79f713ba3cfacfb4	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3,15-Epoxy-6-caryophyllene 10V, Negative-QTOF	splash10-014i-0090000000-eb4aa4fd2af42985176c	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3,15-Epoxy-6-caryophyllene 20V, Negative-QTOF	splash10-014i-1290000000-a5f69b488ae2434d4fd9	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3,15-Epoxy-6-caryophyllene 40V, Negative-QTOF	splash10-01p6-5910000000-9413d949dee0fd789546	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3,15-Epoxy-6-caryophyllene 10V, Negative-QTOF	splash10-014i-0090000000-4af4c4ee1c4acef7e18b	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3,15-Epoxy-6-caryophyllene 20V, Negative-QTOF	splash10-014i-0090000000-4af4c4ee1c4acef7e18b	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3,15-Epoxy-6-caryophyllene 40V, Negative-QTOF	splash10-014r-0390000000-087a06ffcc9fcdc6f80c	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3,15-Epoxy-6-caryophyllene 10V, Positive-QTOF	splash10-00di-0090000000-a0be1c695aa70f176aed	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3,15-Epoxy-6-caryophyllene 20V, Positive-QTOF	splash10-00di-0090000000-37a9a1c638122f6cfe40	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3,15-Epoxy-6-caryophyllene 40V, Positive-QTOF	splash10-052u-9830000000-21b2e838e4178e673cf3	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

FDB015738

KNApSAcK ID

C00012473

Chemspider ID

35014250

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

14589073

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

rw1636991

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

(). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .

Showing metabocard for 3,15-Epoxy-6-caryophyllene (HMDB0036793)

MOL for HMDB0036793 (3,15-Epoxy-6-caryophyllene)

3D MOL for HMDB0036793 (3,15-Epoxy-6-caryophyllene)

3D SDF for HMDB0036793 (3,15-Epoxy-6-caryophyllene)

3D-SDF for HMDB0036793 (3,15-Epoxy-6-caryophyllene)

PDB for HMDB0036793 (3,15-Epoxy-6-caryophyllene)

3D PDB for HMDB0036793 (3,15-Epoxy-6-caryophyllene)

SMILES for HMDB0036793 (3,15-Epoxy-6-caryophyllene)

INCHI for HMDB0036793 (3,15-Epoxy-6-caryophyllene)

Structure for HMDB0036793 (3,15-Epoxy-6-caryophyllene)

3D Structure for HMDB0036793 (3,15-Epoxy-6-caryophyllene)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

GC-MS Spectra

MS/MS Spectra