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Showing metabocard for Isomenthone (HMDB0034972)

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Record Information
Version5.0
StatusDetected but not Quantified
Creation Date2012-09-11 19:54:24 UTC
Update Date2023-02-21 17:24:30 UTC
HMDB IDHMDB0034972
Secondary Accession Numbers
  • HMDB0059864
  • HMDB34972
  • HMDB59864
Metabolite Identification
Common NameIsomenthone
DescriptionIsomenthone belongs to the class of organic compounds known as menthane monoterpenoids. These are monoterpenoids with a structure based on the o-, m-, or p-menthane backbone. P-menthane consists of the cyclohexane ring with a methyl group and a (2-methyl)-propyl group at the 1 and 4 ring position, respectively. The o- and m- menthanes are much rarer, and presumably arise by alkyl migration of p-menthanes. Based on a literature review a small amount of articles have been published on Isomenthone.
Structure
Data?1677000270
MOL3D MOLSDF3D SDFPDB3D PDBSMILESInChI

MOL for HMDB0034972 (Isomenthone)


  Mrv1652305261918452D          

 11 11  0  0  0  0            999 V2000
   -1.8973    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6118    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6118   -0.4126    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8973   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1828   -0.4126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1828    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4683    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8973    1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3262   -0.8251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4683    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2461    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  6  1  0  0  0  0
  2  3  1  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  6  0  0  0
  3  9  1  6  0  0  0
  7 10  1  0  0  0  0
  7 11  1  0  0  0  0
  1  8  2  0  0  0  0
M  END
Download

3D MOL for HMDB0034972 (Isomenthone)

HMDB0034972
     RDKit          3D
Isomenthone
 29 29  0  0  0  0  0  0  0  0999 V2000
   -3.0421    0.6110   -0.9485 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0843   -0.2992   -0.2812 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2783   -0.1971    1.2176 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6584   -0.1566   -0.6905 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1540   -1.1823    0.1137 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5485   -1.1570   -0.4693 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1873    0.2063   -0.3372 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4092    0.0488    0.5502 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2464    1.2428    0.2170 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0495    1.1424   -0.4828 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5770    2.1539   -0.8694 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2965    1.5209   -0.3290 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7532    0.9301   -1.9646 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0340    0.0908   -1.0731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3863   -1.3570   -0.5446 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2950    0.1808    1.4548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5599    0.4747    1.6980 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1823   -1.1865    1.7056 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5197   -0.4524   -1.7509 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2829   -2.1693   -0.0298 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2186   -0.8597    1.1806 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1233   -1.9523    0.0562 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4357   -1.4070   -1.5541 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5812    0.5480   -1.3309 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7961    1.0182    0.9162 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2185   -0.4680   -0.0421 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1840   -0.6414    1.3959 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7369    2.2289    0.0851 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1598    1.0883    1.3118 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  2  0
 10  4  1  0
  1 12  1  0
  1 13  1  0
  1 14  1  0
  2 15  1  0
  3 16  1  0
  3 17  1  0
  3 18  1  0
  4 19  1  6
  5 20  1  0
  5 21  1  0
  6 22  1  0
  6 23  1  0
  7 24  1  6
  8 25  1  0
  8 26  1  0
  8 27  1  0
  9 28  1  0
  9 29  1  0
M  END
Download

3D SDF for HMDB0034972 (Isomenthone)


  Mrv1652305261918452D          

 11 11  0  0  0  0            999 V2000
   -1.8973    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6118    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6118   -0.4126    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8973   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1828   -0.4126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1828    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4683    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8973    1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3262   -0.8251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4683    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2461    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  6  1  0  0  0  0
  2  3  1  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  6  0  0  0
  3  9  1  6  0  0  0
  7 10  1  0  0  0  0
  7 11  1  0  0  0  0
  1  8  2  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0034972

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(C)[C@@H]1CC[C@H](C)CC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C10H18O/c1-7(2)9-5-4-8(3)6-10(9)11/h7-9H,4-6H2,1-3H3/t8-,9-/m0/s1

> <INCHI_KEY>
NFLGAXVYCFJBMK-IUCAKERBSA-N

> <FORMULA>
C10H18O

> <MOLECULAR_WEIGHT>
154.2493

> <EXACT_MASS>
154.135765198

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
29

> <JCHEM_AVERAGE_POLARIZABILITY>
18.670992107592912

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,5S)-5-methyl-2-(propan-2-yl)cyclohexan-1-one

> <ALOGPS_LOGP>
2.65

> <JCHEM_LOGP>
3.0497874006666668

> <ALOGPS_LOGS>
-2.77

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-7.420780675838815

> <JCHEM_POLAR_SURFACE_AREA>
17.07

> <JCHEM_REFRACTIVITY>
46.5201

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.65e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(-)-isomenthone

> <JCHEM_VEBER_RULE>
1

$$$$
Download

3D-SDF for HMDB0034972 (Isomenthone)

HMDB0034972
     RDKit          3D
Isomenthone
 29 29  0  0  0  0  0  0  0  0999 V2000
   -3.0421    0.6110   -0.9485 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0843   -0.2992   -0.2812 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2783   -0.1971    1.2176 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6584   -0.1566   -0.6905 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1540   -1.1823    0.1137 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5485   -1.1570   -0.4693 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1873    0.2063   -0.3372 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4092    0.0488    0.5502 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2464    1.2428    0.2170 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0495    1.1424   -0.4828 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5770    2.1539   -0.8694 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2965    1.5209   -0.3290 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7532    0.9301   -1.9646 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0340    0.0908   -1.0731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3863   -1.3570   -0.5446 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2950    0.1808    1.4548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5599    0.4747    1.6980 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1823   -1.1865    1.7056 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5197   -0.4524   -1.7509 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2829   -2.1693   -0.0298 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2186   -0.8597    1.1806 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1233   -1.9523    0.0562 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4357   -1.4070   -1.5541 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5812    0.5480   -1.3309 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7961    1.0182    0.9162 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2185   -0.4680   -0.0421 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1840   -0.6414    1.3959 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7369    2.2289    0.0851 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1598    1.0883    1.3118 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  2  0
 10  4  1  0
  1 12  1  0
  1 13  1  0
  1 14  1  0
  2 15  1  0
  3 16  1  0
  3 17  1  0
  3 18  1  0
  4 19  1  6
  5 20  1  0
  5 21  1  0
  6 22  1  0
  6 23  1  0
  7 24  1  6
  8 25  1  0
  8 26  1  0
  8 27  1  0
  9 28  1  0
  9 29  1  0
M  END
Download

PDB for HMDB0034972 (Isomenthone)

HEADER    PROTEIN                                 26-MAY-19   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   26-MAY-19         0                                  
HETATM    1  C   UNK     0      -3.542   1.540   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.875   0.770   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.875  -0.770   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -3.542  -1.540   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.208  -0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.208   0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.874   1.540   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -3.542   3.080   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -6.209  -1.540   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.874   3.080   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.459   0.770   0.000  0.00  0.00           C+0
CONECT    1    2    6    8                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4    9                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    1    5    7                                                  
CONECT    7    6   10   11                                                  
CONECT    8    1                                                            
CONECT    9    3                                                            
CONECT   10    7                                                            
CONECT   11    7                                                            
MASTER        0    0    0    0    0    0    0    0   11    0   22    0
END
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3D PDB for HMDB0034972 (Isomenthone)

COMPND    HMDB0034972
HETATM    1  C1  UNL     1      -3.042   0.611  -0.949  1.00  0.00           C  
HETATM    2  C2  UNL     1      -2.084  -0.299  -0.281  1.00  0.00           C  
HETATM    3  C3  UNL     1      -2.278  -0.197   1.218  1.00  0.00           C  
HETATM    4  C4  UNL     1      -0.658  -0.157  -0.691  1.00  0.00           C  
HETATM    5  C5  UNL     1       0.154  -1.182   0.114  1.00  0.00           C  
HETATM    6  C6  UNL     1       1.548  -1.157  -0.469  1.00  0.00           C  
HETATM    7  C7  UNL     1       2.187   0.206  -0.337  1.00  0.00           C  
HETATM    8  C8  UNL     1       3.409   0.049   0.550  1.00  0.00           C  
HETATM    9  C9  UNL     1       1.246   1.243   0.217  1.00  0.00           C  
HETATM   10  C10 UNL     1      -0.050   1.142  -0.483  1.00  0.00           C  
HETATM   11  O1  UNL     1      -0.577   2.154  -0.869  1.00  0.00           O  
HETATM   12  H1  UNL     1      -3.297   1.521  -0.329  1.00  0.00           H  
HETATM   13  H2  UNL     1      -2.753   0.930  -1.965  1.00  0.00           H  
HETATM   14  H3  UNL     1      -4.034   0.091  -1.073  1.00  0.00           H  
HETATM   15  H4  UNL     1      -2.386  -1.357  -0.545  1.00  0.00           H  
HETATM   16  H5  UNL     1      -3.295   0.181   1.455  1.00  0.00           H  
HETATM   17  H6  UNL     1      -1.560   0.475   1.698  1.00  0.00           H  
HETATM   18  H7  UNL     1      -2.182  -1.187   1.706  1.00  0.00           H  
HETATM   19  H8  UNL     1      -0.520  -0.452  -1.751  1.00  0.00           H  
HETATM   20  H9  UNL     1      -0.283  -2.169  -0.030  1.00  0.00           H  
HETATM   21  H10 UNL     1       0.219  -0.860   1.181  1.00  0.00           H  
HETATM   22  H11 UNL     1       2.123  -1.952   0.056  1.00  0.00           H  
HETATM   23  H12 UNL     1       1.436  -1.407  -1.554  1.00  0.00           H  
HETATM   24  H13 UNL     1       2.581   0.548  -1.331  1.00  0.00           H  
HETATM   25  H14 UNL     1       3.796   1.018   0.916  1.00  0.00           H  
HETATM   26  H15 UNL     1       4.219  -0.468  -0.042  1.00  0.00           H  
HETATM   27  H16 UNL     1       3.184  -0.641   1.396  1.00  0.00           H  
HETATM   28  H17 UNL     1       1.737   2.229   0.085  1.00  0.00           H  
HETATM   29  H18 UNL     1       1.160   1.088   1.312  1.00  0.00           H  
CONECT    1    2   12   13   14
CONECT    2    3    4   15
CONECT    3   16   17   18
CONECT    4    5   10   19
CONECT    5    6   20   21
CONECT    6    7   22   23
CONECT    7    8    9   24
CONECT    8   25   26   27
CONECT    9   10   28   29
CONECT   10   11   11
END
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SMILES for HMDB0034972 (Isomenthone)

CC(C)[C@@H]1CC[C@H](C)CC1=O
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INCHI for HMDB0034972 (Isomenthone)

InChI=1S/C10H18O/c1-7(2)9-5-4-8(3)6-10(9)11/h7-9H,4-6H2,1-3H3/t8-,9-/m0/s1
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View in JSmolView Stereo Labels
Synonyms
ValueSource
(1S,4S)-(-)-p-Menthan-3-oneChEBI
(1S,4S)-p-Menthan-3-oneChEBI
(2S,5S)-2-Isopropyl-5-methylcyclohexanoneChEBI
(2S-cis)-5-Methyl-2-(1-methylethyl)cyclohexanoneChEBI
L-IsomenthoneChEBI
IsomenthoneMeSH
(-)-IsomenthoneHMDB
(1S,4S)-IsomenthoneHMDB
(2S,5S)-2-Isopropyl-5-methylcyclohexan-1-oneHMDB
(2S,5S)-5-Methyl-2-(1-methylethyl)cyclohexanoneHMDB
alpha-IsomenthoneHMDB
cis-MenthoneHMDB
cis-p-Menthan-3-oneHMDB
cis-p-MenthoneHMDB
dl-IsomenthoneHMDB
α-IsomenthoneHMDB
Chemical FormulaC10H18O
Average Molecular Weight154.2493
Monoisotopic Molecular Weight154.135765198
IUPAC Name(2S,5S)-5-methyl-2-(propan-2-yl)cyclohexan-1-one
Traditional Name(-)-isomenthone
CAS Registry Number18309-28-9
SMILES
CC(C)[C@@H]1CC[C@H](C)CC1=O
InChI Identifier
InChI=1S/C10H18O/c1-7(2)9-5-4-8(3)6-10(9)11/h7-9H,4-6H2,1-3H3/t8-,9-/m0/s1
InChI KeyNFLGAXVYCFJBMK-IUCAKERBSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as menthane monoterpenoids. These are monoterpenoids with a structure based on the o-, m-, or p-menthane backbone. P-menthane consists of the cyclohexane ring with a methyl group and a (2-methyl)-propyl group at the 1 and 4 ring position, respectively. The o- and m- menthanes are much rarer, and presumably arise by alkyl migration of p-menthanes.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassPrenol lipids
Sub ClassMonoterpenoids
Direct ParentMenthane monoterpenoids
Alternative Parents
Substituents
  • P-menthane monoterpenoid
  • Monocyclic monoterpenoid
  • Cyclic ketone
  • Ketone
  • Organic oxygen compound
  • Organic oxide
  • Hydrocarbon derivative
  • Organooxygen compound
  • Carbonyl group
  • Aliphatic homomonocyclic compound
Molecular FrameworkAliphatic homomonocyclic compounds
External Descriptors
Ontology
Physiological effect
Organoleptic effect
Disposition
Biological locationSource
ProcessNot Available
RoleNot Available
Physical Properties
StateNot Available
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling Point205.00 to 208.00 °C. @ 760.00 mm HgThe Good Scents Company Information System
Water Solubility180.5 mg/L @ 25 °C (est)The Good Scents Company Information System
LogP2.625 (est)The Good Scents Company Information System
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility0.26 g/LALOGPS
logP2.65ALOGPS
logP3.05ChemAxon
logS-2.8ALOGPS
pKa (Strongest Basic)-7.4ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count1ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area17.07 ŲChemAxon
Rotatable Bond Count1ChemAxon
Refractivity46.52 m³·mol⁻¹ChemAxon
Polarizability18.67 ųChemAxon
Number of Rings1ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DarkChem[M+H]+133.96631661259
DarkChem[M-H]-132.15531661259
DeepCCS[M+H]+136.75730932474
DeepCCS[M-H]-133.2730932474
DeepCCS[M-2H]-170.3430932474
DeepCCS[M+Na]+145.87930932474
AllCCS[M+H]+133.532859911
AllCCS[M+H-H2O]+129.132859911
AllCCS[M+NH4]+137.632859911
AllCCS[M+Na]+138.832859911
AllCCS[M-H]-140.032859911
AllCCS[M+Na-2H]-141.632859911
AllCCS[M+HCOO]-143.532859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
IsomenthoneCC(C)[C@@H]1CC[C@H](C)CC1=O1485.7Standard polar33892256
IsomenthoneCC(C)[C@@H]1CC[C@H](C)CC1=O1142.9Standard non polar33892256
IsomenthoneCC(C)[C@@H]1CC[C@H](C)CC1=O1146.9Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
Isomenthone,1TMS,isomer #1CC(C)C1=C(O[Si](C)(C)C)C[C@@H](C)CC11342.3Semi standard non polar33892256
Isomenthone,1TMS,isomer #1CC(C)C1=C(O[Si](C)(C)C)C[C@@H](C)CC11360.6Standard non polar33892256
Isomenthone,1TMS,isomer #2CC(C)[C@@H]1CC[C@H](C)C=C1O[Si](C)(C)C1290.0Semi standard non polar33892256
Isomenthone,1TMS,isomer #2CC(C)[C@@H]1CC[C@H](C)C=C1O[Si](C)(C)C1346.5Standard non polar33892256
Isomenthone,1TBDMS,isomer #1CC(C)C1=C(O[Si](C)(C)C(C)(C)C)C[C@@H](C)CC11565.8Semi standard non polar33892256
Isomenthone,1TBDMS,isomer #1CC(C)C1=C(O[Si](C)(C)C(C)(C)C)C[C@@H](C)CC11544.0Standard non polar33892256
Isomenthone,1TBDMS,isomer #2CC(C)[C@@H]1CC[C@H](C)C=C1O[Si](C)(C)C(C)(C)C1493.2Semi standard non polar33892256
Isomenthone,1TBDMS,isomer #2CC(C)[C@@H]1CC[C@H](C)C=C1O[Si](C)(C)C(C)(C)C1503.7Standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Isomenthone GC-MS (Non-derivatized) - 70eV, Positivesplash10-06r7-9300000000-1d150f2cf0a23dbfef0b2017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Isomenthone GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Isomenthone 10V, Positive-QTOFsplash10-0a4i-0900000000-fa99f8c083212e4f2fc32016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Isomenthone 20V, Positive-QTOFsplash10-0bt9-9800000000-7bf975ea31bcef83aa612016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Isomenthone 40V, Positive-QTOFsplash10-0aor-9000000000-3f8923896797c44866932016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Isomenthone 10V, Negative-QTOFsplash10-0udi-0900000000-d55afdef2faae68197a62016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Isomenthone 20V, Negative-QTOFsplash10-0udi-0900000000-91ec697d11dad181a3422016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Isomenthone 40V, Negative-QTOFsplash10-01oy-9600000000-7933610ac6051fc8ef812016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Isomenthone 10V, Negative-QTOFsplash10-0udi-0900000000-d2363ae8d4dbdcccda802021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Isomenthone 20V, Negative-QTOFsplash10-0udi-0900000000-084e13e285859f435a612021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Isomenthone 40V, Negative-QTOFsplash10-0gbc-9700000000-57929498deae48afce7a2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Isomenthone 10V, Positive-QTOFsplash10-0bti-3900000000-5b9ac9ca9aaff729e2d12021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Isomenthone 20V, Positive-QTOFsplash10-0532-9200000000-ac0243da1ad4aa3d859e2021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Isomenthone 40V, Positive-QTOFsplash10-0006-9000000000-d3a7bbb5abb9a0381a392021-09-25Wishart LabView Spectrum

IR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted IR SpectrumIR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M+H]+)2023-02-04FELIX labView Spectrum
Predicted IR SpectrumIR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M+Na]+)2023-02-04FELIX labView Spectrum
Biological Properties
Cellular Locations
  • Extracellular
  • Membrane
Biospecimen Locations
  • Saliva
Tissue LocationsNot Available
Pathways
Normal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
SalivaDetected but not QuantifiedNot QuantifiedAdult (>18 years old)Not SpecifiedNormal details
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB014639
KNApSAcK IDC00010904 C00037333
Chemspider ID4937714
KEGG Compound IDC17125
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkMenthone
METLIN IDNot Available
PubChem Compound6432469
PDB IDNot Available
ChEBI ID36496
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDrw1507821
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General References
  1. Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. [PubMed:11413487 ]
  2. 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 ]
  3. 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 ]
  4. 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 ]
  5. (). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .
  6. Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.