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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 17:48:34 UTC

Update Date

2022-03-07 02:53:17 UTC

HMDB ID

HMDB0032220

Secondary Accession Numbers

HMDB32220

Metabolite Identification

Common Name

Dihydronootkatone

Description

Dihydronootkatone 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 Dihydronootkatone.

Structure

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

HMDB0032220
     RDKit          3D
Dihydronootkatone
 40 41  0  0  0  0  0  0  0  0999 V2000
    3.6908   -1.4875    0.0055 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0445   -0.3556   -0.2165 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8171    0.9190   -0.2550 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5707   -0.3870   -0.4155 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0329   -1.7897   -0.3091 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4629   -1.8430   -0.2967 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1692   -0.5489   -0.2792 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5883   -0.1829   -1.7116 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5022   -0.7893    0.4466 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3459    0.4430    0.5237 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5737    1.4378    1.3557 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0450    2.4912    1.7210 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1733    1.0028    1.6874 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5133    0.6105    0.3541 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6868    1.8654   -0.5184 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9456    0.4779    0.6578 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7662   -1.4409    0.1521 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2453   -2.4706    0.0522 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2973    1.7184   -0.7872 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1320    1.2174    0.7637 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7529    0.7024   -0.8198 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3931    0.0149   -1.4363 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5005   -2.4118   -1.0919 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3695   -2.1856    0.6721 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7636   -2.3917   -1.2393 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8301   -2.5271    0.5156 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1216    0.7657   -1.7678 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7642   -0.2883   -2.4276 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3243   -0.9929   -1.9896 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0732   -1.5531   -0.1555 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3509   -1.1899    1.4582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6604    0.8542   -0.4376 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2568    0.1984    1.0920 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1573    0.1619    2.4069 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6353    1.8790    2.0604 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3352    1.7141   -1.5375 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7195    2.2639   -0.4484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0508    2.6407   -0.0003 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1394   -0.0246    1.6239 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4059    1.4817    0.5916 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  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  1  0
 11 12  2  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
 16  4  1  0
 14  7  1  0
  1 17  1  0
  1 18  1  0
  3 19  1  0
  3 20  1  0
  3 21  1  0
  4 22  1  0
  5 23  1  0
  5 24  1  0
  6 25  1  0
  6 26  1  0
  8 27  1  0
  8 28  1  0
  8 29  1  0
  9 30  1  0
  9 31  1  0
 10 32  1  0
 10 33  1  0
 13 34  1  0
 13 35  1  0
 15 36  1  0
 15 37  1  0
 15 38  1  0
 16 39  1  0
 16 40  1  0
M  END


  Mrv0541 05061306242D          

 16 17  0  0  0  0            999 V2000
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  7  5  1  0  0  0  0
  8  6  1  0  0  0  0
 11  1  2  0  0  0  0
 11  2  1  0  0  0  0
 12  5  1  0  0  0  0
 12  9  1  0  0  0  0
 12 11  1  0  0  0  0
 13  6  1  0  0  0  0
 13 10  1  0  0  0  0
 14  3  1  0  0  0  0
 14  7  1  0  0  0  0
 14  8  1  0  0  0  0
 15  4  1  0  0  0  0
 15  9  1  0  0  0  0
 15 10  1  0  0  0  0
 15 14  1  0  0  0  0
 16 13  2  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0032220

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(=C)C1CCC2(C)CCC(=O)CC2(C)C1

> <INCHI_IDENTIFIER>
InChI=1S/C15H24O/c1-11(2)12-5-7-14(3)8-6-13(16)10-15(14,4)9-12/h12H,1,5-10H2,2-4H3

> <INCHI_KEY>
VESUMYPXHVXDJI-UHFFFAOYSA-N

> <FORMULA>
C15H24O

> <MOLECULAR_WEIGHT>
220.3505

> <EXACT_MASS>
220.18271539

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_AVERAGE_POLARIZABILITY>
26.65782320614788

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4a,8a-dimethyl-7-(prop-1-en-2-yl)-decahydronaphthalen-2-one

> <ALOGPS_LOGP>
4.10

> <JCHEM_LOGP>
3.758699171333334

> <ALOGPS_LOGS>
-4.45

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-7.3577452639460095

> <JCHEM_POLAR_SURFACE_AREA>
17.07

> <JCHEM_REFRACTIVITY>
67.17029999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.78e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4a,8a-dimethyl-7-(prop-1-en-2-yl)-hexahydro-1H-naphthalen-2-one

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0032220
     RDKit          3D
Dihydronootkatone
 40 41  0  0  0  0  0  0  0  0999 V2000
    3.6908   -1.4875    0.0055 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0445   -0.3556   -0.2165 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8171    0.9190   -0.2550 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5707   -0.3870   -0.4155 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0329   -1.7897   -0.3091 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4629   -1.8430   -0.2967 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1692   -0.5489   -0.2792 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5883   -0.1829   -1.7116 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5022   -0.7893    0.4466 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3459    0.4430    0.5237 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5737    1.4378    1.3557 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0450    2.4912    1.7210 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1733    1.0028    1.6874 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5133    0.6105    0.3541 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6868    1.8654   -0.5184 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9456    0.4779    0.6578 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7662   -1.4409    0.1521 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2453   -2.4706    0.0522 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2973    1.7184   -0.7872 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1320    1.2174    0.7637 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7529    0.7024   -0.8198 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3931    0.0149   -1.4363 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5005   -2.4118   -1.0919 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3695   -2.1856    0.6721 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7636   -2.3917   -1.2393 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8301   -2.5271    0.5156 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1216    0.7657   -1.7678 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7642   -0.2883   -2.4276 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3243   -0.9929   -1.9896 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0732   -1.5531   -0.1555 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3509   -1.1899    1.4582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6604    0.8542   -0.4376 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2568    0.1984    1.0920 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1573    0.1619    2.4069 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6353    1.8790    2.0604 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3352    1.7141   -1.5375 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7195    2.2639   -0.4484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0508    2.6407   -0.0003 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1394   -0.0246    1.6239 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4059    1.4817    0.5916 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  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  1  0
 11 12  2  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
 16  4  1  0
 14  7  1  0
  1 17  1  0
  1 18  1  0
  3 19  1  0
  3 20  1  0
  3 21  1  0
  4 22  1  0
  5 23  1  0
  5 24  1  0
  6 25  1  0
  6 26  1  0
  8 27  1  0
  8 28  1  0
  8 29  1  0
  9 30  1  0
  9 31  1  0
 10 32  1  0
 10 33  1  0
 13 34  1  0
 13 35  1  0
 15 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       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.335   3.080   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.335  -1.540   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.002   0.000   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       9.336  -0.770   0.000  0.00  0.00           O+0
CONECT    1   11                                                            
CONECT    2   11                                                            
CONECT    3   14                                                            
CONECT    4   15                                                            
CONECT    5    7   12                                                       
CONECT    6    8   13                                                       
CONECT    7    5   14                                                       
CONECT    8    6   14                                                       
CONECT    9   12   15                                                       
CONECT   10   13   15                                                       
CONECT   11    1    2   12                                                  
CONECT   12    5    9   11                                                  
CONECT   13    6   10   16                                                  
CONECT   14    3    7    8   15                                             
CONECT   15    4    9   10   14                                             
CONECT   16   13                                                            
MASTER        0    0    0    0    0    0    0    0   16    0   34    0
END

COMPND    HMDB0032220
HETATM    1  C1  UNL     1       3.691  -1.487   0.005  1.00  0.00           C  
HETATM    2  C2  UNL     1       3.045  -0.356  -0.216  1.00  0.00           C  
HETATM    3  C3  UNL     1       3.817   0.919  -0.255  1.00  0.00           C  
HETATM    4  C4  UNL     1       1.571  -0.387  -0.415  1.00  0.00           C  
HETATM    5  C5  UNL     1       1.033  -1.790  -0.309  1.00  0.00           C  
HETATM    6  C6  UNL     1      -0.463  -1.843  -0.297  1.00  0.00           C  
HETATM    7  C7  UNL     1      -1.169  -0.549  -0.279  1.00  0.00           C  
HETATM    8  C8  UNL     1      -1.588  -0.183  -1.712  1.00  0.00           C  
HETATM    9  C9  UNL     1      -2.502  -0.789   0.447  1.00  0.00           C  
HETATM   10  C10 UNL     1      -3.346   0.443   0.524  1.00  0.00           C  
HETATM   11  C11 UNL     1      -2.574   1.438   1.356  1.00  0.00           C  
HETATM   12  O1  UNL     1      -3.045   2.491   1.721  1.00  0.00           O  
HETATM   13  C12 UNL     1      -1.173   1.003   1.687  1.00  0.00           C  
HETATM   14  C13 UNL     1      -0.513   0.610   0.354  1.00  0.00           C  
HETATM   15  C14 UNL     1      -0.687   1.865  -0.518  1.00  0.00           C  
HETATM   16  C15 UNL     1       0.946   0.478   0.658  1.00  0.00           C  
HETATM   17  H1  UNL     1       4.766  -1.441   0.152  1.00  0.00           H  
HETATM   18  H2  UNL     1       3.245  -2.471   0.052  1.00  0.00           H  
HETATM   19  H3  UNL     1       3.297   1.718  -0.787  1.00  0.00           H  
HETATM   20  H4  UNL     1       4.132   1.217   0.764  1.00  0.00           H  
HETATM   21  H5  UNL     1       4.753   0.702  -0.820  1.00  0.00           H  
HETATM   22  H6  UNL     1       1.393   0.015  -1.436  1.00  0.00           H  
HETATM   23  H7  UNL     1       1.500  -2.412  -1.092  1.00  0.00           H  
HETATM   24  H8  UNL     1       1.370  -2.186   0.672  1.00  0.00           H  
HETATM   25  H9  UNL     1      -0.764  -2.392  -1.239  1.00  0.00           H  
HETATM   26  H10 UNL     1      -0.830  -2.527   0.516  1.00  0.00           H  
HETATM   27  H11 UNL     1      -2.122   0.766  -1.768  1.00  0.00           H  
HETATM   28  H12 UNL     1      -0.764  -0.288  -2.428  1.00  0.00           H  
HETATM   29  H13 UNL     1      -2.324  -0.993  -1.990  1.00  0.00           H  
HETATM   30  H14 UNL     1      -3.073  -1.553  -0.155  1.00  0.00           H  
HETATM   31  H15 UNL     1      -2.351  -1.190   1.458  1.00  0.00           H  
HETATM   32  H16 UNL     1      -3.660   0.854  -0.438  1.00  0.00           H  
HETATM   33  H17 UNL     1      -4.257   0.198   1.092  1.00  0.00           H  
HETATM   34  H18 UNL     1      -1.157   0.162   2.407  1.00  0.00           H  
HETATM   35  H19 UNL     1      -0.635   1.879   2.060  1.00  0.00           H  
HETATM   36  H20 UNL     1      -0.335   1.714  -1.537  1.00  0.00           H  
HETATM   37  H21 UNL     1      -1.719   2.264  -0.448  1.00  0.00           H  
HETATM   38  H22 UNL     1      -0.051   2.641  -0.000  1.00  0.00           H  
HETATM   39  H23 UNL     1       1.139  -0.025   1.624  1.00  0.00           H  
HETATM   40  H24 UNL     1       1.406   1.482   0.592  1.00  0.00           H  
CONECT    1    2    2   17   18
CONECT    2    3    4
CONECT    3   19   20   21
CONECT    4    5   16   22
CONECT    5    6   23   24
CONECT    6    7   25   26
CONECT    7    8    9   14
CONECT    8   27   28   29
CONECT    9   10   30   31
CONECT   10   11   32   33
CONECT   11   12   12   13
CONECT   13   14   34   35
CONECT   14   15   16
CONECT   15   36   37   38
CONECT   16   39   40
END

HMDB0032220
     RDKit          3D
Dihydronootkatone
 40 41  0  0  0  0  0  0  0  0999 V2000
    3.6908   -1.4875    0.0055 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0445   -0.3556   -0.2165 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8171    0.9190   -0.2550 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5707   -0.3870   -0.4155 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0329   -1.7897   -0.3091 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4629   -1.8430   -0.2967 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1692   -0.5489   -0.2792 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5883   -0.1829   -1.7116 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5022   -0.7893    0.4466 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3459    0.4430    0.5237 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5737    1.4378    1.3557 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0450    2.4912    1.7210 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1733    1.0028    1.6874 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5133    0.6105    0.3541 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6868    1.8654   -0.5184 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9456    0.4779    0.6578 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7662   -1.4409    0.1521 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2453   -2.4706    0.0522 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2973    1.7184   -0.7872 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1320    1.2174    0.7637 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7529    0.7024   -0.8198 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3931    0.0149   -1.4363 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5005   -2.4118   -1.0919 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3695   -2.1856    0.6721 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7636   -2.3917   -1.2393 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8301   -2.5271    0.5156 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1216    0.7657   -1.7678 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7642   -0.2883   -2.4276 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3243   -0.9929   -1.9896 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0732   -1.5531   -0.1555 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3509   -1.1899    1.4582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6604    0.8542   -0.4376 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2568    0.1984    1.0920 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1573    0.1619    2.4069 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6353    1.8790    2.0604 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3352    1.7141   -1.5375 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7195    2.2639   -0.4484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0508    2.6407   -0.0003 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1394   -0.0246    1.6239 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4059    1.4817    0.5916 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  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  1  0
 11 12  2  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
 16  4  1  0
 14  7  1  0
  1 17  1  0
  1 18  1  0
  3 19  1  0
  3 20  1  0
  3 21  1  0
  4 22  1  0
  5 23  1  0
  5 24  1  0
  6 25  1  0
  6 26  1  0
  8 27  1  0
  8 28  1  0
  8 29  1  0
  9 30  1  0
  9 31  1  0
 10 32  1  0
 10 33  1  0
 13 34  1  0
 13 35  1  0
 15 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

Not Available

Chemical Formula

C₁₅H₂₄O

Average Molecular Weight

220.3505

Monoisotopic Molecular Weight

220.18271539

IUPAC Name

4a,8a-dimethyl-7-(prop-1-en-2-yl)-decahydronaphthalen-2-one

Traditional Name

4a,8a-dimethyl-7-(prop-1-en-2-yl)-hexahydro-1H-naphthalen-2-one

CAS Registry Number

20489-53-6

SMILES

CC(=C)C1CCC2(C)CCC(=O)CC2(C)C1

InChI Identifier

InChI=1S/C15H24O/c1-11(2)12-5-7-14(3)8-6-13(16)10-15(14,4)9-12/h12H,1,5-10H2,2-4H3

InChI Key

VESUMYPXHVXDJI-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

Valerane sequiterpene
Sesquiterpenoid
Cyclic ketone
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

Cytoplasm (HMDB: HMDB0032220)
Cell membrane (HMDB: HMDB0032220)

Cellular substructure

Extracellular (HMDB: HMDB0032220)
Membrane (HMDB: HMDB0032220)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0032220)

Source

Endogenous

Endogenous (HMDB: HMDB0032220)

Animal

Animal (HMDB: HMDB0032220)

Exogenous

Food

Food (HMDB: HMDB0032220)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid peroxidation (HMDB: HMDB0032220)

Biochemical process

Fatty acid metabolism (HMDB: HMDB0032220)

Cellular process

Cell signaling (HMDB: HMDB0032220)

Biochemical pathway

Lipid metabolism pathway (HMDB: HMDB0032220)

Role

Biological role

Membrane stabilizer (HMDB: HMDB0032220)

Nutrient

Nutrient (HMDB: HMDB0032220)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0032220)

Emulsifier (HMDB: HMDB0032220)

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	0.0078 g/L	ALOGPS
logP	4.1	ALOGPS
logP	3.76	ChemAxon
logS	-4.4	ALOGPS
pKa (Strongest Basic)	-7.4	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	67.17 m³·mol⁻¹	ChemAxon
Polarizability	26.66 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	150.03	31661259
DarkChem	[M-H]-	149.644	31661259
DeepCCS	[M+H]+	155.301	30932474
DeepCCS	[M-H]-	152.943	30932474
DeepCCS	[M-2H]-	186.806	30932474
DeepCCS	[M+Na]+	161.654	30932474
AllCCS	[M+H]+	153.0	32859911
AllCCS	[M+H-H2O]+	149.2	32859911
AllCCS	[M+NH4]+	156.5	32859911
AllCCS	[M+Na]+	157.5	32859911
AllCCS	[M-H]-	160.5	32859911
AllCCS	[M+Na-2H]-	161.1	32859911
AllCCS	[M+HCOO]-	161.8	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Dihydronootkatone	CC(=C)C1CCC2(C)CCC(=O)CC2(C)C1	2233.0	Standard polar	33892256
Dihydronootkatone	CC(=C)C1CCC2(C)CCC(=O)CC2(C)C1	1653.3	Standard non polar	33892256
Dihydronootkatone	CC(=C)C1CCC2(C)CCC(=O)CC2(C)C1	1713.1	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Dihydronootkatone,1TMS,isomer #1	C=C(C)C1CCC2(C)CCC(O[Si](C)(C)C)=CC2(C)C1	1808.3	Semi standard non polar	33892256
Dihydronootkatone,1TMS,isomer #1	C=C(C)C1CCC2(C)CCC(O[Si](C)(C)C)=CC2(C)C1	1703.7	Standard non polar	33892256
Dihydronootkatone,1TMS,isomer #2	C=C(C)C1CCC2(C)CC=C(O[Si](C)(C)C)CC2(C)C1	1822.5	Semi standard non polar	33892256
Dihydronootkatone,1TMS,isomer #2	C=C(C)C1CCC2(C)CC=C(O[Si](C)(C)C)CC2(C)C1	1719.0	Standard non polar	33892256
Dihydronootkatone,1TBDMS,isomer #1	C=C(C)C1CCC2(C)CCC(O[Si](C)(C)C(C)(C)C)=CC2(C)C1	2059.1	Semi standard non polar	33892256
Dihydronootkatone,1TBDMS,isomer #1	C=C(C)C1CCC2(C)CCC(O[Si](C)(C)C(C)(C)C)=CC2(C)C1	1892.7	Standard non polar	33892256
Dihydronootkatone,1TBDMS,isomer #2	C=C(C)C1CCC2(C)CC=C(O[Si](C)(C)C(C)(C)C)CC2(C)C1	2082.9	Semi standard non polar	33892256
Dihydronootkatone,1TBDMS,isomer #2	C=C(C)C1CCC2(C)CC=C(O[Si](C)(C)C(C)(C)C)CC2(C)C1	1891.1	Standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Dihydronootkatone GC-MS (Non-derivatized) - 70eV, Positive	splash10-054o-2920000000-73915c3917f1188e6a31	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Dihydronootkatone 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 - Dihydronootkatone 10V, Positive-QTOF	splash10-00di-0290000000-65ba5df93ea0f198edea	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dihydronootkatone 20V, Positive-QTOF	splash10-00gl-2930000000-78e25d1021e02e37c52c	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dihydronootkatone 40V, Positive-QTOF	splash10-016r-6900000000-e4773ce259c0d1c6f8d9	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dihydronootkatone 10V, Negative-QTOF	splash10-014i-0090000000-e73b2e18005f1f84de87	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dihydronootkatone 20V, Negative-QTOF	splash10-014i-0090000000-9ad270217b913b72ca65	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dihydronootkatone 40V, Negative-QTOF	splash10-0udl-4940000000-01c7f38abc485a499514	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dihydronootkatone 10V, Positive-QTOF	splash10-0fk9-0970000000-20e4a8a180ef3e0e0917	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dihydronootkatone 20V, Positive-QTOF	splash10-0002-0900000000-1d88774a0c12428d045f	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dihydronootkatone 40V, Positive-QTOF	splash10-0006-9710000000-9978d158d3d86884d7b8	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dihydronootkatone 10V, Negative-QTOF	splash10-014i-0090000000-4af4c4ee1c4acef7e18b	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dihydronootkatone 20V, Negative-QTOF	splash10-014i-0090000000-4af4c4ee1c4acef7e18b	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dihydronootkatone 40V, Negative-QTOF	splash10-014i-0290000000-e21425b8151949d61562	2021-09-23	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

FDB009290

KNApSAcK ID

Not Available

Chemspider ID

244192

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

277452

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 ]
(). EAFUS: Everything Added to Food in the United States.. .
Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.

Showing metabocard for Dihydronootkatone (HMDB0032220)

MOL for HMDB0032220 (Dihydronootkatone)

3D MOL for HMDB0032220 (Dihydronootkatone)

3D SDF for HMDB0032220 (Dihydronootkatone)

3D-SDF for HMDB0032220 (Dihydronootkatone)

PDB for HMDB0032220 (Dihydronootkatone)

3D PDB for HMDB0032220 (Dihydronootkatone)

SMILES for HMDB0032220 (Dihydronootkatone)

INCHI for HMDB0032220 (Dihydronootkatone)

Structure for HMDB0032220 (Dihydronootkatone)

3D Structure for HMDB0032220 (Dihydronootkatone)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra