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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 21:58:26 UTC

Update Date

2022-03-07 02:55:04 UTC

HMDB ID

HMDB0036797

Secondary Accession Numbers

HMDB36797

Metabolite Identification

Common Name

Mustakone

Description

Mustakone 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 Mustakone.

Structure

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

HMDB0036797
     RDKit          3D
Mustakone
 38 40  0  0  0  0  0  0  0  0999 V2000
    2.2555    2.4460    0.6788 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8319    1.0024    0.6348 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5492    0.0720    1.2717 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1304   -1.3099    1.0181 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7000   -2.3142    1.4782 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9492   -1.4779    0.1536 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1046   -0.4830    0.6746 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4084   -0.9385    0.1010 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5742   -0.0611    0.4724 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7510   -0.0185    1.9502 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5319    1.3061   -0.1035 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3259   -1.2217   -1.3621 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0595   -0.7929   -2.0224 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0575   -0.5647   -1.0445 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4099   -0.4139   -1.6457 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6415    0.5684   -0.0926 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3312    2.4961    0.9950 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6768    2.9085    1.4896 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1241    2.9042   -0.2998 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3509    0.3598    1.9021 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5825   -2.4848   -0.0200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0786   -0.3629    1.7524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6258   -1.9316    0.6031 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4878   -0.5734    0.0480 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8433    0.0349    2.2200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3854   -0.9694    2.4044 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2810    0.8669    2.4310 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2727    1.3517   -1.1698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5809    1.7250   -0.0374 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9282    2.0262    0.5211 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4590   -2.3175   -1.6077 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1866   -0.7351   -1.9102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2322    0.1896   -2.5399 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2948   -1.5269   -2.7833 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4506   -1.0399   -2.5636 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2214   -0.6936   -0.9728 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4981    0.6509   -2.0057 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0615    1.3228   -0.6192 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  2  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
  9 11  1  0
  8 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
 16  2  1  0
 14  6  1  0
 16  7  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  3 20  1  0
  6 21  1  0
  7 22  1  0
  8 23  1  0
  9 24  1  0
 10 25  1  0
 10 26  1  0
 10 27  1  0
 11 28  1  0
 11 29  1  0
 11 30  1  0
 12 31  1  0
 12 32  1  0
 13 33  1  0
 13 34  1  0
 15 35  1  0
 15 36  1  0
 15 37  1  0
 16 38  1  0
M  END

  Mrv0541 02241214542D          

 16 18  0  0  0  0            999 V2000
   -0.7544    0.3632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1400    0.3070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0838    1.0338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6426   -0.3632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4807   -0.1394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4807    0.6982    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7544    1.0895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9781    1.8720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8662   -0.9781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1400   -0.3070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6426   -0.1394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7544    0.6982    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4807    0.9781    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6426   -1.2575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1400   -1.1457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5307   -1.8720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  7  1  0  0  0  0
  1 10  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  3  7  1  0  0  0  0
  3 12  1  0  0  0  0
  4  5  1  0  0  0  0
  4 15  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0036797

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(C)C1CCC2(C)C3C1C2C(=O)C=C3C

> <INCHI_IDENTIFIER>
InChI=1S/C15H22O/c1-8(2)10-5-6-15(4)13-9(3)7-11(16)14(15)12(10)13/h7-8,10,12-14H,5-6H2,1-4H3

> <INCHI_KEY>
CTFSUCDHRVDRKG-UHFFFAOYSA-N

> <FORMULA>
C15H22O

> <MOLECULAR_WEIGHT>
218.3346

> <EXACT_MASS>
218.167065326

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_AVERAGE_POLARIZABILITY>
26.330385385360476

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1,5-dimethyl-8-(propan-2-yl)tricyclo[4.4.0.0²,⁷]dec-4-en-3-one

> <ALOGPS_LOGP>
2.58

> <JCHEM_LOGP>
3.524624765666667

> <ALOGPS_LOGS>
-3.74

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
19.76282435407948

> <JCHEM_PKA_STRONGEST_BASIC>
-4.758814287084403

> <JCHEM_POLAR_SURFACE_AREA>
17.07

> <JCHEM_REFRACTIVITY>
66.4119

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.98e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
8-isopropyl-1,5-dimethyltricyclo[4.4.0.0²,⁷]dec-4-en-3-one

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0036797
     RDKit          3D
Mustakone
 38 40  0  0  0  0  0  0  0  0999 V2000
    2.2555    2.4460    0.6788 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8319    1.0024    0.6348 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5492    0.0720    1.2717 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1304   -1.3099    1.0181 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7000   -2.3142    1.4782 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9492   -1.4779    0.1536 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1046   -0.4830    0.6746 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4084   -0.9385    0.1010 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5742   -0.0611    0.4724 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7510   -0.0185    1.9502 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5319    1.3061   -0.1035 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3259   -1.2217   -1.3621 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0595   -0.7929   -2.0224 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0575   -0.5647   -1.0445 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4099   -0.4139   -1.6457 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6415    0.5684   -0.0926 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3312    2.4961    0.9950 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6768    2.9085    1.4896 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1241    2.9042   -0.2998 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3509    0.3598    1.9021 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5825   -2.4848   -0.0200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0786   -0.3629    1.7524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6258   -1.9316    0.6031 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4878   -0.5734    0.0480 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8433    0.0349    2.2200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3854   -0.9694    2.4044 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2810    0.8669    2.4310 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2727    1.3517   -1.1698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5809    1.7250   -0.0374 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9282    2.0262    0.5211 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4590   -2.3175   -1.6077 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1866   -0.7351   -1.9102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2322    0.1896   -2.5399 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2948   -1.5269   -2.7833 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4506   -1.0399   -2.5636 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2214   -0.6936   -0.9728 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4981    0.6509   -2.0057 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0615    1.3228   -0.6192 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  2  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
  9 11  1  0
  8 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
 16  2  1  0
 14  6  1  0
 16  7  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  3 20  1  0
  6 21  1  0
  7 22  1  0
  8 23  1  0
  9 24  1  0
 10 25  1  0
 10 26  1  0
 10 27  1  0
 11 28  1  0
 11 29  1  0
 11 30  1  0
 12 31  1  0
 12 32  1  0
 13 33  1  0
 13 34  1  0
 15 35  1  0
 15 36  1  0
 15 37  1  0
 16 38  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      -1.408   0.678   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.261   0.573   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.156   1.930   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.200  -0.678   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.764  -0.260   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.764   1.303   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.408   2.034   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.826   3.494   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.617  -1.826   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.261  -0.573   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.200  -0.260   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.408   1.303   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       2.764   1.826   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       1.200  -2.347   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.261  -2.139   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.991  -3.494   0.000  0.00  0.00           C+0
CONECT    1    2    7   10                                                  
CONECT    2    1    3    4                                                  
CONECT    3    2    7   12                                                  
CONECT    4    2    5   15                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    1    3    6    8                                             
CONECT    8    7                                                            
CONECT    9   10                                                            
CONECT   10    1    9   11                                                  
CONECT   11   10   12                                                       
CONECT   12    3   11   13                                                  
CONECT   13   12                                                            
CONECT   14   15                                                            
CONECT   15    4   14   16                                                  
CONECT   16   15                                                            
MASTER        0    0    0    0    0    0    0    0   16    0   36    0
END

COMPND    HMDB0036797
HETATM    1  C1  UNL     1       2.255   2.446   0.679  1.00  0.00           C  
HETATM    2  C2  UNL     1       1.832   1.002   0.635  1.00  0.00           C  
HETATM    3  C3  UNL     1       2.549   0.072   1.272  1.00  0.00           C  
HETATM    4  C4  UNL     1       2.130  -1.310   1.018  1.00  0.00           C  
HETATM    5  O1  UNL     1       2.700  -2.314   1.478  1.00  0.00           O  
HETATM    6  C5  UNL     1       0.949  -1.478   0.154  1.00  0.00           C  
HETATM    7  C6  UNL     1      -0.105  -0.483   0.675  1.00  0.00           C  
HETATM    8  C7  UNL     1      -1.408  -0.939   0.101  1.00  0.00           C  
HETATM    9  C8  UNL     1      -2.574  -0.061   0.472  1.00  0.00           C  
HETATM   10  C9  UNL     1      -2.751  -0.019   1.950  1.00  0.00           C  
HETATM   11  C10 UNL     1      -2.532   1.306  -0.104  1.00  0.00           C  
HETATM   12  C11 UNL     1      -1.326  -1.222  -1.362  1.00  0.00           C  
HETATM   13  C12 UNL     1      -0.059  -0.793  -2.022  1.00  0.00           C  
HETATM   14  C13 UNL     1       1.058  -0.565  -1.045  1.00  0.00           C  
HETATM   15  C14 UNL     1       2.410  -0.414  -1.646  1.00  0.00           C  
HETATM   16  C15 UNL     1       0.642   0.568  -0.093  1.00  0.00           C  
HETATM   17  H1  UNL     1       3.331   2.496   0.995  1.00  0.00           H  
HETATM   18  H2  UNL     1       1.677   2.908   1.490  1.00  0.00           H  
HETATM   19  H3  UNL     1       2.124   2.904  -0.300  1.00  0.00           H  
HETATM   20  H4  UNL     1       3.351   0.360   1.902  1.00  0.00           H  
HETATM   21  H5  UNL     1       0.583  -2.485  -0.020  1.00  0.00           H  
HETATM   22  H6  UNL     1      -0.079  -0.363   1.752  1.00  0.00           H  
HETATM   23  H7  UNL     1      -1.626  -1.932   0.603  1.00  0.00           H  
HETATM   24  H8  UNL     1      -3.488  -0.573   0.048  1.00  0.00           H  
HETATM   25  H9  UNL     1      -3.843   0.035   2.220  1.00  0.00           H  
HETATM   26  H10 UNL     1      -2.385  -0.969   2.404  1.00  0.00           H  
HETATM   27  H11 UNL     1      -2.281   0.867   2.431  1.00  0.00           H  
HETATM   28  H12 UNL     1      -2.273   1.352  -1.170  1.00  0.00           H  
HETATM   29  H13 UNL     1      -3.581   1.725  -0.037  1.00  0.00           H  
HETATM   30  H14 UNL     1      -1.928   2.026   0.521  1.00  0.00           H  
HETATM   31  H15 UNL     1      -1.459  -2.318  -1.608  1.00  0.00           H  
HETATM   32  H16 UNL     1      -2.187  -0.735  -1.910  1.00  0.00           H  
HETATM   33  H17 UNL     1      -0.232   0.190  -2.540  1.00  0.00           H  
HETATM   34  H18 UNL     1       0.295  -1.527  -2.783  1.00  0.00           H  
HETATM   35  H19 UNL     1       2.451  -1.040  -2.564  1.00  0.00           H  
HETATM   36  H20 UNL     1       3.221  -0.694  -0.973  1.00  0.00           H  
HETATM   37  H21 UNL     1       2.498   0.651  -2.006  1.00  0.00           H  
HETATM   38  H22 UNL     1       0.062   1.323  -0.619  1.00  0.00           H  
CONECT    1    2   17   18   19
CONECT    2    3    3   16
CONECT    3    4   20
CONECT    4    5    5    6
CONECT    6    7   14   21
CONECT    7    8   16   22
CONECT    8    9   12   23
CONECT    9   10   11   24
CONECT   10   25   26   27
CONECT   11   28   29   30
CONECT   12   13   31   32
CONECT   13   14   33   34
CONECT   14   15   16
CONECT   15   35   36   37
CONECT   16   38
END

HMDB0036797
     RDKit          3D
Mustakone
 38 40  0  0  0  0  0  0  0  0999 V2000
    2.2555    2.4460    0.6788 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8319    1.0024    0.6348 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5492    0.0720    1.2717 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1304   -1.3099    1.0181 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7000   -2.3142    1.4782 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9492   -1.4779    0.1536 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1046   -0.4830    0.6746 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4084   -0.9385    0.1010 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5742   -0.0611    0.4724 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7510   -0.0185    1.9502 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5319    1.3061   -0.1035 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3259   -1.2217   -1.3621 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0595   -0.7929   -2.0224 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0575   -0.5647   -1.0445 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4099   -0.4139   -1.6457 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6415    0.5684   -0.0926 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3312    2.4961    0.9950 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6768    2.9085    1.4896 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1241    2.9042   -0.2998 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3509    0.3598    1.9021 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5825   -2.4848   -0.0200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0786   -0.3629    1.7524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6258   -1.9316    0.6031 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4878   -0.5734    0.0480 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8433    0.0349    2.2200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3854   -0.9694    2.4044 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2810    0.8669    2.4310 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2727    1.3517   -1.1698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5809    1.7250   -0.0374 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9282    2.0262    0.5211 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4590   -2.3175   -1.6077 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1866   -0.7351   -1.9102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2322    0.1896   -2.5399 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2948   -1.5269   -2.7833 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4506   -1.0399   -2.5636 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2214   -0.6936   -0.9728 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4981    0.6509   -2.0057 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0615    1.3228   -0.6192 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  2  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
  9 11  1  0
  8 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
 16  2  1  0
 14  6  1  0
 16  7  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  3 20  1  0
  6 21  1  0
  7 22  1  0
  8 23  1  0
  9 24  1  0
 10 25  1  0
 10 26  1  0
 10 27  1  0
 11 28  1  0
 11 29  1  0
 11 30  1  0
 12 31  1  0
 12 32  1  0
 13 33  1  0
 13 34  1  0
 15 35  1  0
 15 36  1  0
 15 37  1  0
 16 38  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
Mustakone	MeSH

Chemical Formula

C₁₅H₂₂O

Average Molecular Weight

218.3346

Monoisotopic Molecular Weight

218.167065326

IUPAC Name

1,5-dimethyl-8-(propan-2-yl)tricyclo[4.4.0.0²,⁷]dec-4-en-3-one

Traditional Name

8-isopropyl-1,5-dimethyltricyclo[4.4.0.0²,⁷]dec-4-en-3-one

CAS Registry Number

1209-91-2

SMILES

CC(C)C1CCC2(C)C3C1C2C(=O)C=C3C

InChI Identifier

InChI=1S/C15H22O/c1-8(2)10-5-6-15(4)13-9(3)7-11(16)14(15)12(10)13/h7-8,10,12-14H,5-6H2,1-4H3

InChI Key

CTFSUCDHRVDRKG-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
Cyclohexenone
Ketone
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Ontology

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	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.04 g/L	ALOGPS
logP	2.58	ALOGPS
logP	3.52	ChemAxon
logS	-3.7	ALOGPS
pKa (Strongest Acidic)	19.76	ChemAxon
pKa (Strongest Basic)	-4.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	17.07 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	66.41 m³·mol⁻¹	ChemAxon
Polarizability	26.33 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]+	152.189	31661259
DarkChem	[M-H]-	146.537	31661259
DeepCCS	[M+H]+	156.779	30932474
DeepCCS	[M-H]-	154.421	30932474
DeepCCS	[M-2H]-	187.926	30932474
DeepCCS	[M+Na]+	162.946	30932474
AllCCS	[M+H]+	149.3	32859911
AllCCS	[M+H-H2O]+	145.5	32859911
AllCCS	[M+NH4]+	152.8	32859911
AllCCS	[M+Na]+	153.9	32859911
AllCCS	[M-H]-	160.0	32859911
AllCCS	[M+Na-2H]-	160.2	32859911
AllCCS	[M+HCOO]-	160.5	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Mustakone	CC(C)C1CCC2(C)C3C1C2C(=O)C=C3C	2334.2	Standard polar	33892256
Mustakone	CC(C)C1CCC2(C)C3C1C2C(=O)C=C3C	1680.5	Standard non polar	33892256
Mustakone	CC(C)C1CCC2(C)C3C1C2C(=O)C=C3C	1669.5	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Mustakone,1TMS,isomer #1	CC1=CC(O[Si](C)(C)C)=C2C3C(C(C)C)CCC2(C)C13	1771.0	Semi standard non polar	33892256
Mustakone,1TMS,isomer #1	CC1=CC(O[Si](C)(C)C)=C2C3C(C(C)C)CCC2(C)C13	1737.1	Standard non polar	33892256
Mustakone,1TBDMS,isomer #1	CC1=CC(O[Si](C)(C)C(C)(C)C)=C2C3C(C(C)C)CCC2(C)C13	2017.0	Semi standard non polar	33892256
Mustakone,1TBDMS,isomer #1	CC1=CC(O[Si](C)(C)C(C)(C)C)=C2C3C(C(C)C)CCC2(C)C13	1970.0	Standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Mustakone GC-MS (Non-derivatized) - 70eV, Positive	splash10-0f96-9630000000-27bc630716a6655d9ae4	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Mustakone GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Mustakone 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 - Mustakone 10V, Positive-QTOF	splash10-014i-0090000000-a21a56445fe75e671dbb	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mustakone 20V, Positive-QTOF	splash10-014i-0290000000-5b263dabc940ed67e4aa	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mustakone 40V, Positive-QTOF	splash10-0udr-0890000000-5b1a275efa21e9f0d87a	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mustakone 10V, Negative-QTOF	splash10-014i-0090000000-572ffb7b2ad053f371bd	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mustakone 20V, Negative-QTOF	splash10-014i-0090000000-b2fad3c3171c6312a17d	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mustakone 40V, Negative-QTOF	splash10-0gb9-0690000000-cfda5ab5a256aea1c245	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mustakone 10V, Negative-QTOF	splash10-014i-0090000000-868e2fb00a2cfbf6c529	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mustakone 20V, Negative-QTOF	splash10-014i-0090000000-868e2fb00a2cfbf6c529	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mustakone 40V, Negative-QTOF	splash10-014i-0090000000-2c1a6e4a28ba530a585b	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mustakone 10V, Positive-QTOF	splash10-014i-0090000000-eda9112d52fe3b01c3ae	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mustakone 20V, Positive-QTOF	splash10-014i-0190000000-6d4e5c799b9a7fd7c87a	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mustakone 40V, Positive-QTOF	splash10-0002-4910000000-4f80ff6cd0c7e7e6cca8	2021-09-22	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

FDB015743

KNApSAcK ID

C00021870

Chemspider ID

35014251

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Mustakone

METLIN ID

Not Available

PubChem Compound

12313013

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

rw1857251

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 Mustakone (HMDB0036797)

MOL for HMDB0036797 (Mustakone)

3D MOL for HMDB0036797 (Mustakone)

3D SDF for HMDB0036797 (Mustakone)

3D-SDF for HMDB0036797 (Mustakone)

PDB for HMDB0036797 (Mustakone)

3D PDB for HMDB0036797 (Mustakone)

SMILES for HMDB0036797 (Mustakone)

INCHI for HMDB0036797 (Mustakone)

Structure for HMDB0036797 (Mustakone)

3D Structure for HMDB0036797 (Mustakone)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra