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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-12 02:10:31 UTC

Update Date

2022-03-07 02:56:40 UTC

HMDB ID

HMDB0040615

Secondary Accession Numbers

HMDB40615

Metabolite Identification

Common Name

4,5-Dihydrovomifoliol

Description

4,5-Dihydrovomifoliol belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. Based on a literature review a small amount of articles have been published on 4,5-Dihydrovomifoliol.

Structure

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

HMDB0040615
     RDKit          3D
4,5-Dihydrovomifoliol
 38 38  0  0  0  0  0  0  0  0999 V2000
    4.3950    0.7241    0.1918 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3811   -0.3465    0.4786 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2404   -0.5794    1.8406 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0854    0.0662   -0.1470 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9047   -0.3145    0.3410 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3817    0.1233   -0.3193 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0432    0.2540   -1.6903 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7798    1.4430    0.1821 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1565    2.3804   -0.9754 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8851    1.4903    1.1837 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7846    0.3402    1.1827 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9759    0.4914    1.3249 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2042   -0.9970    1.0054 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3603   -0.9775   -0.2370 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6407   -2.3323   -0.2879 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3293   -0.9907   -1.4134 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3946    0.2605    0.0103 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4175    1.5033    0.9700 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1087    1.2250   -0.7532 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7371   -1.2956   -0.0169 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9355   -1.2610    2.0763 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0727    0.7041   -1.0393 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9092   -0.9451    1.2227 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5602   -0.4902   -1.9383 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1041    1.9371    0.6534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6304    1.7760   -1.7685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8804    3.1437   -0.6531 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2203    2.8358   -1.3984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4651    1.5788    2.2301 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4834    2.4149    1.0479 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0302   -1.7149    0.8267 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6485   -1.3636    1.8895 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3983   -3.0828   -0.6051 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3335   -2.6326    0.7407 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1824   -2.3254   -1.0040 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2727   -0.4613   -1.1637 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8892   -0.5448   -2.3217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6347   -2.0371   -1.6657 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  2  0
  5  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  8 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
 14  6  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  2 20  1  0
  3 21  1  0
  4 22  1  0
  5 23  1  0
  7 24  1  0
  8 25  1  0
  9 26  1  0
  9 27  1  0
  9 28  1  0
 10 29  1  0
 10 30  1  0
 13 31  1  0
 13 32  1  0
 15 33  1  0
 15 34  1  0
 15 35  1  0
 16 36  1  0
 16 37  1  0
 16 38  1  0
M  END


  Mrv0541 05061311592D          

 16 16  0  0  0  0            999 V2000
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2182    4.0520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8125    0.6817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2822    1.6002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4663    2.6447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1842    1.8695    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
    0.0000    0.0000    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
   -0.0640    3.2767    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
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8764    3.1335    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2448    1.8695    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  2  0  0  0  0
  9  1  1  0  0  0  0
  9  7  1  0  0  0  0
 10  2  1  0  0  0  0
 10  5  1  0  0  0  0
 11  7  1  0  0  0  0
 11  8  1  0  0  0  0
 12  3  1  0  0  0  0
 12  4  1  0  0  0  0
 12  8  1  0  0  0  0
 13  6  1  0  0  0  0
 13  9  1  0  0  0  0
 13 12  1  0  0  0  0
 14 10  1  0  0  0  0
 15 11  2  0  0  0  0
 16 13  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0040615

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(O)\C=C\C1(O)C(C)CC(=O)CC1(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C13H22O3/c1-9-7-11(15)8-12(3,4)13(9,16)6-5-10(2)14/h5-6,9-10,14,16H,7-8H2,1-4H3/b6-5+

> <INCHI_KEY>
IHDJYDVWNNFPHR-AATRIKPKSA-N

> <FORMULA>
C13H22O3

> <MOLECULAR_WEIGHT>
226.312

> <EXACT_MASS>
226.15689457

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_AVERAGE_POLARIZABILITY>
25.28797157640865

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-hydroxy-4-[(1E)-3-hydroxybut-1-en-1-yl]-3,3,5-trimethylcyclohexan-1-one

> <ALOGPS_LOGP>
1.21

> <JCHEM_LOGP>
1.3868796400000007

> <ALOGPS_LOGS>
-1.87

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.327770369330086

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.773766186292981

> <JCHEM_PKA_STRONGEST_BASIC>
-2.6678995147267166

> <JCHEM_POLAR_SURFACE_AREA>
57.53

> <JCHEM_REFRACTIVITY>
64.17750000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.06e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-hydroxy-4-[(1E)-3-hydroxybut-1-en-1-yl]-3,3,5-trimethylcyclohexan-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0040615
     RDKit          3D
4,5-Dihydrovomifoliol
 38 38  0  0  0  0  0  0  0  0999 V2000
    4.3950    0.7241    0.1918 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3811   -0.3465    0.4786 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2404   -0.5794    1.8406 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0854    0.0662   -0.1470 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9047   -0.3145    0.3410 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3817    0.1233   -0.3193 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0432    0.2540   -1.6903 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7798    1.4430    0.1821 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1565    2.3804   -0.9754 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8851    1.4903    1.1837 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7846    0.3402    1.1827 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9759    0.4914    1.3249 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2042   -0.9970    1.0054 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3603   -0.9775   -0.2370 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6407   -2.3323   -0.2879 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3293   -0.9907   -1.4134 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3946    0.2605    0.0103 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4175    1.5033    0.9700 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1087    1.2250   -0.7532 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7371   -1.2956   -0.0169 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9355   -1.2610    2.0763 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0727    0.7041   -1.0393 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9092   -0.9451    1.2227 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5602   -0.4902   -1.9383 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1041    1.9371    0.6534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6304    1.7760   -1.7685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8804    3.1437   -0.6531 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2203    2.8358   -1.3984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4651    1.5788    2.2301 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4834    2.4149    1.0479 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0302   -1.7149    0.8267 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6485   -1.3636    1.8895 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3983   -3.0828   -0.6051 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3335   -2.6326    0.7407 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1824   -2.3254   -1.0040 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2727   -0.4613   -1.1637 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8892   -0.5448   -2.3217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6347   -2.0371   -1.6657 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  2  0
  5  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  8 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
 14  6  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  2 20  1  0
  3 21  1  0
  4 22  1  0
  5 23  1  0
  7 24  1  0
  8 25  1  0
  9 26  1  0
  9 27  1  0
  9 28  1  0
 10 29  1  0
 10 30  1  0
 13 31  1  0
 13 32  1  0
 15 33  1  0
 15 34  1  0
 15 35  1  0
 16 36  1  0
 16 37  1  0
 16 38  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       4.001   2.310   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.407   7.564   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.517   1.273   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.527   2.987   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.870   4.937   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.344   3.490   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.119   6.117   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       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -1.636   5.849   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0       1.334  -2.310   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0       2.324   3.490   0.000  0.00  0.00           O+0
CONECT    1    9                                                            
CONECT    2   10                                                            
CONECT    3   12                                                            
CONECT    4   12                                                            
CONECT    5    6   10                                                       
CONECT    6    5   13                                                       
CONECT    7    9   11                                                       
CONECT    8   11   12                                                       
CONECT    9    1    7   13                                                  
CONECT   10    2    5   14                                                  
CONECT   11    7    8   15                                                  
CONECT   12    3    4    8   13                                             
CONECT   13    6    9   12   16                                             
CONECT   14   10                                                            
CONECT   15   11                                                            
CONECT   16   13                                                            
MASTER        0    0    0    0    0    0    0    0   16    0   32    0
END

COMPND    HMDB0040615
HETATM    1  C1  UNL     1       4.395   0.724   0.192  1.00  0.00           C  
HETATM    2  C2  UNL     1       3.381  -0.347   0.479  1.00  0.00           C  
HETATM    3  O1  UNL     1       3.240  -0.579   1.841  1.00  0.00           O  
HETATM    4  C3  UNL     1       2.085   0.066  -0.147  1.00  0.00           C  
HETATM    5  C4  UNL     1       0.905  -0.315   0.341  1.00  0.00           C  
HETATM    6  C5  UNL     1      -0.382   0.123  -0.319  1.00  0.00           C  
HETATM    7  O2  UNL     1      -0.043   0.254  -1.690  1.00  0.00           O  
HETATM    8  C6  UNL     1      -0.780   1.443   0.182  1.00  0.00           C  
HETATM    9  C7  UNL     1      -1.157   2.380  -0.975  1.00  0.00           C  
HETATM   10  C8  UNL     1      -1.885   1.490   1.184  1.00  0.00           C  
HETATM   11  C9  UNL     1      -2.785   0.340   1.183  1.00  0.00           C  
HETATM   12  O3  UNL     1      -3.976   0.491   1.325  1.00  0.00           O  
HETATM   13  C10 UNL     1      -2.204  -0.997   1.005  1.00  0.00           C  
HETATM   14  C11 UNL     1      -1.360  -0.977  -0.237  1.00  0.00           C  
HETATM   15  C12 UNL     1      -0.641  -2.332  -0.288  1.00  0.00           C  
HETATM   16  C13 UNL     1      -2.329  -0.991  -1.413  1.00  0.00           C  
HETATM   17  H1  UNL     1       5.395   0.260   0.010  1.00  0.00           H  
HETATM   18  H2  UNL     1       4.417   1.503   0.970  1.00  0.00           H  
HETATM   19  H3  UNL     1       4.109   1.225  -0.753  1.00  0.00           H  
HETATM   20  H4  UNL     1       3.737  -1.296  -0.017  1.00  0.00           H  
HETATM   21  H5  UNL     1       3.935  -1.261   2.076  1.00  0.00           H  
HETATM   22  H6  UNL     1       2.073   0.704  -1.039  1.00  0.00           H  
HETATM   23  H7  UNL     1       0.909  -0.945   1.223  1.00  0.00           H  
HETATM   24  H8  UNL     1       0.560  -0.490  -1.938  1.00  0.00           H  
HETATM   25  H9  UNL     1       0.104   1.937   0.653  1.00  0.00           H  
HETATM   26  H10 UNL     1      -1.630   1.776  -1.769  1.00  0.00           H  
HETATM   27  H11 UNL     1      -1.880   3.144  -0.653  1.00  0.00           H  
HETATM   28  H12 UNL     1      -0.220   2.836  -1.398  1.00  0.00           H  
HETATM   29  H13 UNL     1      -1.465   1.579   2.230  1.00  0.00           H  
HETATM   30  H14 UNL     1      -2.483   2.415   1.048  1.00  0.00           H  
HETATM   31  H15 UNL     1      -3.030  -1.715   0.827  1.00  0.00           H  
HETATM   32  H16 UNL     1      -1.649  -1.364   1.889  1.00  0.00           H  
HETATM   33  H17 UNL     1      -1.398  -3.083  -0.605  1.00  0.00           H  
HETATM   34  H18 UNL     1      -0.333  -2.633   0.741  1.00  0.00           H  
HETATM   35  H19 UNL     1       0.182  -2.325  -1.004  1.00  0.00           H  
HETATM   36  H20 UNL     1      -3.273  -0.461  -1.164  1.00  0.00           H  
HETATM   37  H21 UNL     1      -1.889  -0.545  -2.322  1.00  0.00           H  
HETATM   38  H22 UNL     1      -2.635  -2.037  -1.666  1.00  0.00           H  
CONECT    1    2   17   18   19
CONECT    2    3    4   20
CONECT    3   21
CONECT    4    5    5   22
CONECT    5    6   23
CONECT    6    7    8   14
CONECT    7   24
CONECT    8    9   10   25
CONECT    9   26   27   28
CONECT   10   11   29   30
CONECT   11   12   12   13
CONECT   13   14   31   32
CONECT   14   15   16
CONECT   15   33   34   35
CONECT   16   36   37   38
END

HMDB0040615
     RDKit          3D
4,5-Dihydrovomifoliol
 38 38  0  0  0  0  0  0  0  0999 V2000
    4.3950    0.7241    0.1918 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3811   -0.3465    0.4786 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2404   -0.5794    1.8406 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0854    0.0662   -0.1470 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9047   -0.3145    0.3410 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3817    0.1233   -0.3193 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0432    0.2540   -1.6903 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7798    1.4430    0.1821 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1565    2.3804   -0.9754 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8851    1.4903    1.1837 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7846    0.3402    1.1827 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9759    0.4914    1.3249 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2042   -0.9970    1.0054 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3603   -0.9775   -0.2370 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6407   -2.3323   -0.2879 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3293   -0.9907   -1.4134 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3946    0.2605    0.0103 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4175    1.5033    0.9700 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1087    1.2250   -0.7532 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7371   -1.2956   -0.0169 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9355   -1.2610    2.0763 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0727    0.7041   -1.0393 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9092   -0.9451    1.2227 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5602   -0.4902   -1.9383 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1041    1.9371    0.6534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6304    1.7760   -1.7685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8804    3.1437   -0.6531 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2203    2.8358   -1.3984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4651    1.5788    2.2301 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4834    2.4149    1.0479 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0302   -1.7149    0.8267 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6485   -1.3636    1.8895 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3983   -3.0828   -0.6051 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3335   -2.6326    0.7407 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1824   -2.3254   -1.0040 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2727   -0.4613   -1.1637 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8892   -0.5448   -2.3217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6347   -2.0371   -1.6657 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  2  0
  5  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  8 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
 14  6  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  2 20  1  0
  3 21  1  0
  4 22  1  0
  5 23  1  0
  7 24  1  0
  8 25  1  0
  9 26  1  0
  9 27  1  0
  9 28  1  0
 10 29  1  0
 10 30  1  0
 13 31  1  0
 13 32  1  0
 15 33  1  0
 15 34  1  0
 15 35  1  0
 16 36  1  0
 16 37  1  0
 16 38  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
(5-chloro-2-Hydroxybenzylidene)-malononitrile	HMDB
(5-chloro-2-HYDROXYBENZYLIDENE)malononitrile	HMDB
2-(5-chloro-2-Hydroxybenzylidene)malononitrile	HMDB
5-chloro-2-Hydroxybenzylidenemalononitrile	HMDB

Chemical Formula

C₁₃H₂₂O₃

Average Molecular Weight

226.312

Monoisotopic Molecular Weight

226.15689457

IUPAC Name

4-hydroxy-4-[(1E)-3-hydroxybut-1-en-1-yl]-3,3,5-trimethylcyclohexan-1-one

Traditional Name

4-hydroxy-4-[(1E)-3-hydroxybut-1-en-1-yl]-3,3,5-trimethylcyclohexan-1-one

CAS Registry Number

142173-08-8

SMILES

CC(O)\C=C\C1(O)C(C)CC(=O)CC1(C)C

InChI Identifier

InChI=1S/C13H22O3/c1-9-7-11(15)8-12(3,4)13(9,16)6-5-10(2)14/h5-6,9-10,14,16H,7-8H2,1-4H3/b6-5+

InChI Key

IHDJYDVWNNFPHR-AATRIKPKSA-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

Sesquiterpenoid
Megastigmane sesquiterpenoid
Cyclofarsesane sesquiterpenoid
Ionone derivative
Cyclic alcohol
Tertiary alcohol
Ketone
Secondary alcohol
Cyclic ketone
Organooxygen compound
Alcohol
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Carbonyl group
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic homomonocyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Route of exposure

Enteral

Ingestion (HMDB: HMDB0040615)

Source

Endogenous

Endogenous (HMDB: HMDB0040615)

Plant

Plant (HMDB: HMDB0040615)

Animal

Animal (HMDB: HMDB0040615)

Exogenous

Food

Food (HMDB: HMDB0040615)

Fruit

Fruits (FooDB: FOOD00871)

Beverage

Alcoholic beverage

Alcoholic beverages (FooDB: FOOD00854)

Exogenous (HMDB: HMDB0040615)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid Peroxidation (HMDB: HMDB0040615)

Biochemical pathway

Metabolic pathway

Fatty Acid Metabolism (HMDB: HMDB0040615)

Lipid metabolism pathway (HMDB: HMDB0040615)

Cellular process

Cell signaling (HMDB: HMDB0040615)

Biochemical process

Lipid transport (HMDB: HMDB0040615)

Role

Biological role

Energy source (HMDB: HMDB0040615)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0040615)

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	1818 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	3.06 g/L	ALOGPS
logP	1.21	ALOGPS
logP	1.39	ChemAxon
logS	-1.9	ALOGPS
pKa (Strongest Acidic)	13.77	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	57.53 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	64.18 m³·mol⁻¹	ChemAxon
Polarizability	25.29 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	154.755	31661259
DarkChem	[M-H]-	152.998	31661259
DeepCCS	[M+H]+	163.326	30932474
DeepCCS	[M-H]-	160.968	30932474
DeepCCS	[M-2H]-	193.854	30932474
DeepCCS	[M+Na]+	169.419	30932474
AllCCS	[M+H]+	153.7	32859911
AllCCS	[M+H-H2O]+	150.0	32859911
AllCCS	[M+NH4]+	157.2	32859911
AllCCS	[M+Na]+	158.2	32859911
AllCCS	[M-H]-	157.7	32859911
AllCCS	[M+Na-2H]-	158.6	32859911
AllCCS	[M+HCOO]-	159.6	32859911

Predicted Retention Times

Underivatized

Chromatographic Method	Retention Time	Reference
Measured using a Waters Acquity ultraperformance liquid chromatography (UPLC) ethylene-bridged hybrid (BEH) C18 column (100 mm × 2.1 mm; 1.7 μmparticle diameter). Predicted by Afia on May 17, 2022.	3.56 minutes	32390414
Predicted by Siyang on May 30, 2022	10.0497 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	1.96 minutes	32390414
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	1749.7 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	208.8 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	124.2 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	155.9 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	69.8 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	377.3 seconds	40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid	386.1 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	62.1 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	779.6 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	311.6 seconds	40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid	991.1 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	235.8 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	272.1 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	260.8 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	205.8 seconds	40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water	8.8 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
4,5-Dihydrovomifoliol	CC(O)\C=C\C1(O)C(C)CC(=O)CC1(C)C	2932.0	Standard polar	33892256
4,5-Dihydrovomifoliol	CC(O)\C=C\C1(O)C(C)CC(=O)CC1(C)C	1654.1	Standard non polar	33892256
4,5-Dihydrovomifoliol	CC(O)\C=C\C1(O)C(C)CC(=O)CC1(C)C	1769.7	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
4,5-Dihydrovomifoliol,1TMS,isomer #1	CC(/C=C/C1(O)C(C)CC(=O)CC1(C)C)O[Si](C)(C)C	1849.2	Semi standard non polar	33892256
4,5-Dihydrovomifoliol,1TMS,isomer #2	CC(O)/C=C/C1(O[Si](C)(C)C)C(C)CC(=O)CC1(C)C	1872.7	Semi standard non polar	33892256
4,5-Dihydrovomifoliol,1TMS,isomer #3	CC(O)/C=C/C1(O)C(C)CC(O[Si](C)(C)C)=CC1(C)C	1892.2	Semi standard non polar	33892256
4,5-Dihydrovomifoliol,1TMS,isomer #4	CC(O)/C=C/C1(O)C(C)C=C(O[Si](C)(C)C)CC1(C)C	1917.6	Semi standard non polar	33892256
4,5-Dihydrovomifoliol,2TMS,isomer #1	CC(/C=C/C1(O[Si](C)(C)C)C(C)CC(=O)CC1(C)C)O[Si](C)(C)C	1911.7	Semi standard non polar	33892256
4,5-Dihydrovomifoliol,2TMS,isomer #2	CC(/C=C/C1(O)C(C)CC(O[Si](C)(C)C)=CC1(C)C)O[Si](C)(C)C	1884.4	Semi standard non polar	33892256
4,5-Dihydrovomifoliol,2TMS,isomer #3	CC(/C=C/C1(O)C(C)C=C(O[Si](C)(C)C)CC1(C)C)O[Si](C)(C)C	1915.3	Semi standard non polar	33892256
4,5-Dihydrovomifoliol,2TMS,isomer #4	CC(O)/C=C/C1(O[Si](C)(C)C)C(C)CC(O[Si](C)(C)C)=CC1(C)C	1913.0	Semi standard non polar	33892256
4,5-Dihydrovomifoliol,2TMS,isomer #5	CC(O)/C=C/C1(O[Si](C)(C)C)C(C)C=C(O[Si](C)(C)C)CC1(C)C	1932.9	Semi standard non polar	33892256
4,5-Dihydrovomifoliol,3TMS,isomer #1	CC(/C=C/C1(O[Si](C)(C)C)C(C)CC(O[Si](C)(C)C)=CC1(C)C)O[Si](C)(C)C	1919.3	Semi standard non polar	33892256
4,5-Dihydrovomifoliol,3TMS,isomer #1	CC(/C=C/C1(O[Si](C)(C)C)C(C)CC(O[Si](C)(C)C)=CC1(C)C)O[Si](C)(C)C	1934.8	Standard non polar	33892256
4,5-Dihydrovomifoliol,3TMS,isomer #2	CC(/C=C/C1(O[Si](C)(C)C)C(C)C=C(O[Si](C)(C)C)CC1(C)C)O[Si](C)(C)C	1963.8	Semi standard non polar	33892256
4,5-Dihydrovomifoliol,3TMS,isomer #2	CC(/C=C/C1(O[Si](C)(C)C)C(C)C=C(O[Si](C)(C)C)CC1(C)C)O[Si](C)(C)C	1931.8	Standard non polar	33892256
4,5-Dihydrovomifoliol,1TBDMS,isomer #1	CC(/C=C/C1(O)C(C)CC(=O)CC1(C)C)O[Si](C)(C)C(C)(C)C	2109.3	Semi standard non polar	33892256
4,5-Dihydrovomifoliol,1TBDMS,isomer #2	CC(O)/C=C/C1(O[Si](C)(C)C(C)(C)C)C(C)CC(=O)CC1(C)C	2140.7	Semi standard non polar	33892256
4,5-Dihydrovomifoliol,1TBDMS,isomer #3	CC(O)/C=C/C1(O)C(C)CC(O[Si](C)(C)C(C)(C)C)=CC1(C)C	2136.2	Semi standard non polar	33892256
4,5-Dihydrovomifoliol,1TBDMS,isomer #4	CC(O)/C=C/C1(O)C(C)C=C(O[Si](C)(C)C(C)(C)C)CC1(C)C	2153.6	Semi standard non polar	33892256
4,5-Dihydrovomifoliol,2TBDMS,isomer #1	CC(/C=C/C1(O[Si](C)(C)C(C)(C)C)C(C)CC(=O)CC1(C)C)O[Si](C)(C)C(C)(C)C	2369.3	Semi standard non polar	33892256
4,5-Dihydrovomifoliol,2TBDMS,isomer #2	CC(/C=C/C1(O)C(C)CC(O[Si](C)(C)C(C)(C)C)=CC1(C)C)O[Si](C)(C)C(C)(C)C	2360.0	Semi standard non polar	33892256
4,5-Dihydrovomifoliol,2TBDMS,isomer #3	CC(/C=C/C1(O)C(C)C=C(O[Si](C)(C)C(C)(C)C)CC1(C)C)O[Si](C)(C)C(C)(C)C	2384.1	Semi standard non polar	33892256
4,5-Dihydrovomifoliol,2TBDMS,isomer #4	CC(O)/C=C/C1(O[Si](C)(C)C(C)(C)C)C(C)CC(O[Si](C)(C)C(C)(C)C)=CC1(C)C	2412.0	Semi standard non polar	33892256
4,5-Dihydrovomifoliol,2TBDMS,isomer #5	CC(O)/C=C/C1(O[Si](C)(C)C(C)(C)C)C(C)C=C(O[Si](C)(C)C(C)(C)C)CC1(C)C	2426.4	Semi standard non polar	33892256
4,5-Dihydrovomifoliol,3TBDMS,isomer #1	CC(/C=C/C1(O[Si](C)(C)C(C)(C)C)C(C)CC(O[Si](C)(C)C(C)(C)C)=CC1(C)C)O[Si](C)(C)C(C)(C)C	2613.0	Semi standard non polar	33892256
4,5-Dihydrovomifoliol,3TBDMS,isomer #1	CC(/C=C/C1(O[Si](C)(C)C(C)(C)C)C(C)CC(O[Si](C)(C)C(C)(C)C)=CC1(C)C)O[Si](C)(C)C(C)(C)C	2564.5	Standard non polar	33892256
4,5-Dihydrovomifoliol,3TBDMS,isomer #2	CC(/C=C/C1(O[Si](C)(C)C(C)(C)C)C(C)C=C(O[Si](C)(C)C(C)(C)C)CC1(C)C)O[Si](C)(C)C(C)(C)C	2630.5	Semi standard non polar	33892256
4,5-Dihydrovomifoliol,3TBDMS,isomer #2	CC(/C=C/C1(O[Si](C)(C)C(C)(C)C)C(C)C=C(O[Si](C)(C)C(C)(C)C)CC1(C)C)O[Si](C)(C)C(C)(C)C	2556.9	Standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 4,5-Dihydrovomifoliol GC-MS (Non-derivatized) - 70eV, Positive	splash10-0694-9620000000-3a0ce82491e71c30c811	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 4,5-Dihydrovomifoliol GC-MS (2 TMS) - 70eV, Positive	splash10-0abi-9185000000-f1713daecd626afad091	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 4,5-Dihydrovomifoliol 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 - 4,5-Dihydrovomifoliol 10V, Positive-QTOF	splash10-0a4l-1590000000-3106b55539f1c501ba05	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4,5-Dihydrovomifoliol 20V, Positive-QTOF	splash10-0a4l-6940000000-0f5568244a67ccbe436e	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4,5-Dihydrovomifoliol 40V, Positive-QTOF	splash10-0a4i-9500000000-7b29f610c32dee73871e	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4,5-Dihydrovomifoliol 10V, Negative-QTOF	splash10-004i-0190000000-36965830774bec66e789	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4,5-Dihydrovomifoliol 20V, Negative-QTOF	splash10-0a6r-2290000000-f947d8c88277fa02b88f	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4,5-Dihydrovomifoliol 40V, Negative-QTOF	splash10-0a4l-9510000000-45f93a16989a0dcd0afb	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4,5-Dihydrovomifoliol 10V, Negative-QTOF	splash10-004i-0490000000-7c134a760547b2e4fc33	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4,5-Dihydrovomifoliol 20V, Negative-QTOF	splash10-052r-1900000000-ae1ee135ddcdd155a105	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4,5-Dihydrovomifoliol 40V, Negative-QTOF	splash10-0a4r-1910000000-b3fa6be81e8a7e07ed01	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4,5-Dihydrovomifoliol 10V, Positive-QTOF	splash10-056u-1980000000-6aba3441ff89f552089e	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4,5-Dihydrovomifoliol 20V, Positive-QTOF	splash10-0a4r-4910000000-47c01630fcc7f17a7b1b	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4,5-Dihydrovomifoliol 40V, Positive-QTOF	splash10-0597-9200000000-7b8683e427bfc4edd8c8	2021-09-22	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Cytoplasm
Extracellular
Membrane

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB020406

KNApSAcK ID

C00054618

Chemspider ID

16166638

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

23136584

PDB ID

Not Available

ChEBI ID

138758

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

rw1884761

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 4,5-Dihydrovomifoliol (HMDB0040615)

MOL for HMDB0040615 (4,5-Dihydrovomifoliol)

3D MOL for HMDB0040615 (4,5-Dihydrovomifoliol)

3D SDF for HMDB0040615 (4,5-Dihydrovomifoliol)

3D-SDF for HMDB0040615 (4,5-Dihydrovomifoliol)

PDB for HMDB0040615 (4,5-Dihydrovomifoliol)

3D PDB for HMDB0040615 (4,5-Dihydrovomifoliol)

SMILES for HMDB0040615 (4,5-Dihydrovomifoliol)

INCHI for HMDB0040615 (4,5-Dihydrovomifoliol)

Structure for HMDB0040615 (4,5-Dihydrovomifoliol)

3D Structure for HMDB0040615 (4,5-Dihydrovomifoliol)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra