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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 21:14:39 UTC

Update Date

2023-02-21 17:25:11 UTC

HMDB ID

HMDB0036184

Secondary Accession Numbers

HMDB36184

Metabolite Identification

Common Name

7,8-Dehydro-3,4-dihydro-beta-ionol

Description

7,8-Dehydro-3,4-dihydro-beta-ionol 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 7,8-Dehydro-3,4-dihydro-beta-ionol.

Structure

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

HMDB0036184
     RDKit          3D
7,8-Dehydro-3,4-dihydro-beta-ionol
 36 36  0  0  0  0  0  0  0  0999 V2000
    0.4367   -2.4475    1.3992 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5547   -1.6502    0.6278 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5322   -0.3100    0.6072 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5036    0.3796    1.3685 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5053    1.1840    0.6135 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3271    0.3668   -0.3724 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3125    1.2880   -1.1090 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1376   -0.5490    0.3367 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5795    0.4218   -0.1281 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0426    1.5111   -1.0470 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3166    1.2212    0.9918 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5452   -0.3720   -0.9123 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4888   -1.8165   -0.8290 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5553   -2.4066   -0.1072 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5641   -2.1368    2.4418 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0864   -3.5233    1.4907 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3800   -2.5415    0.8285 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0226    1.1342    2.0429 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0368   -0.2554    2.1057 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3159    1.5626    1.3427 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1542    2.1082    0.1502 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7331   -0.1246   -1.1539 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8224    1.7289   -2.0095 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1225    0.6185   -1.4722 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7421    2.0363   -0.4424 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7390   -0.9392   -0.3608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0103    2.5075   -0.5560 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8497    1.6549   -1.8407 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1484    1.2314   -1.6029 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4993    0.5560    1.8390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2807    1.5841    0.5986 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6494    2.0650    1.2292 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5265   -0.0901   -1.9946 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5854   -0.0738   -0.5662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2103   -2.4113   -1.3573 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5217   -3.5122   -0.0522 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  6  8  1  0
  3  9  1  0
  9 10  1  0
  9 11  1  0
  9 12  1  0
 12 13  1  0
 13 14  2  0
 14  2  1  0
  1 15  1  0
  1 16  1  0
  1 17  1  0
  4 18  1  0
  4 19  1  0
  5 20  1  0
  5 21  1  0
  6 22  1  0
  7 23  1  0
  7 24  1  0
  7 25  1  0
  8 26  1  0
 10 27  1  0
 10 28  1  0
 10 29  1  0
 11 30  1  0
 11 31  1  0
 11 32  1  0
 12 33  1  0
 12 34  1  0
 13 35  1  0
 14 36  1  0
M  END

  Mrv0541 02241219152D          

 14 14  0  0  0  0            999 V2000
   -2.1438    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1438   -0.8245    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4292    0.4123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7147    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7147   -0.8245    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4292   -1.2368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8415    1.1269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0170    1.1269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0001    0.4123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4292    0.4123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1438    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4292    1.2368    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0001   -1.2368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  3  1  0  0  0  0
  2  6  2  0  0  0  0
  3  4  1  0  0  0  0
  3  7  1  0  0  0  0
  3  8  1  0  0  0  0
  4  5  2  0  0  0  0
  4  9  1  0  0  0  0
  5  6  1  0  0  0  0
  5 14  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0036184

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(O)CCC1=C(C)C=CCC1(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C13H22O/c1-10-6-5-9-13(3,4)12(10)8-7-11(2)14/h5-6,11,14H,7-9H2,1-4H3

> <INCHI_KEY>
WPGXAVCJKGSOBD-UHFFFAOYSA-N

> <FORMULA>
C13H22O

> <MOLECULAR_WEIGHT>
194.3132

> <EXACT_MASS>
194.167065326

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_AVERAGE_POLARIZABILITY>
24.015992875294206

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-(2,6,6-trimethylcyclohexa-1,3-dien-1-yl)butan-2-ol

> <ALOGPS_LOGP>
4.29

> <JCHEM_LOGP>
2.8863911743333337

> <ALOGPS_LOGS>
-2.70

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
17.716205174621084

> <JCHEM_PKA_STRONGEST_BASIC>
-1.6107318566207374

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
62.9764

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.88e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-(2,6,6-trimethylcyclohexa-1,3-dien-1-yl)butan-2-ol

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0036184
     RDKit          3D
7,8-Dehydro-3,4-dihydro-beta-ionol
 36 36  0  0  0  0  0  0  0  0999 V2000
    0.4367   -2.4475    1.3992 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5547   -1.6502    0.6278 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5322   -0.3100    0.6072 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5036    0.3796    1.3685 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5053    1.1840    0.6135 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3271    0.3668   -0.3724 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3125    1.2880   -1.1090 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1376   -0.5490    0.3367 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5795    0.4218   -0.1281 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0426    1.5111   -1.0470 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3166    1.2212    0.9918 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5452   -0.3720   -0.9123 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4888   -1.8165   -0.8290 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5553   -2.4066   -0.1072 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5641   -2.1368    2.4418 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0864   -3.5233    1.4907 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3800   -2.5415    0.8285 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0226    1.1342    2.0429 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0368   -0.2554    2.1057 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3159    1.5626    1.3427 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1542    2.1082    0.1502 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7331   -0.1246   -1.1539 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8224    1.7289   -2.0095 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1225    0.6185   -1.4722 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7421    2.0363   -0.4424 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7390   -0.9392   -0.3608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0103    2.5075   -0.5560 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8497    1.6549   -1.8407 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1484    1.2314   -1.6029 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4993    0.5560    1.8390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2807    1.5841    0.5986 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6494    2.0650    1.2292 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5265   -0.0901   -1.9946 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5854   -0.0738   -0.5662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2103   -2.4113   -1.3573 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5217   -3.5122   -0.0522 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  6  8  1  0
  3  9  1  0
  9 10  1  0
  9 11  1  0
  9 12  1  0
 12 13  1  0
 13 14  2  0
 14  2  1  0
  1 15  1  0
  1 16  1  0
  1 17  1  0
  4 18  1  0
  4 19  1  0
  5 20  1  0
  5 21  1  0
  6 22  1  0
  7 23  1  0
  7 24  1  0
  7 25  1  0
  8 26  1  0
 10 27  1  0
 10 28  1  0
 10 29  1  0
 11 30  1  0
 11 31  1  0
 11 32  1  0
 12 33  1  0
 12 34  1  0
 13 35  1  0
 14 36  1  0
M  END

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0      -4.002   0.000   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.002  -1.539   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.668   0.770   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.334   0.000   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.334  -1.539   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.668  -2.309   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -3.437   2.104   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.898   2.104   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.000   0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.334   0.000   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.668   0.770   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.002   0.000   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       2.668   2.309   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -0.000  -2.309   0.000  0.00  0.00           C+0
CONECT    1    2    3                                                       
CONECT    2    1    6                                                       
CONECT    3    1    4    7    8                                             
CONECT    4    3    5    9                                                  
CONECT    5    4    6   14                                                  
CONECT    6    2    5                                                       
CONECT    7    3                                                            
CONECT    8    3                                                            
CONECT    9    4   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14    5                                                            
MASTER        0    0    0    0    0    0    0    0   14    0   28    0
END

COMPND    HMDB0036184
HETATM    1  C1  UNL     1       0.437  -2.447   1.399  1.00  0.00           C  
HETATM    2  C2  UNL     1      -0.555  -1.650   0.628  1.00  0.00           C  
HETATM    3  C3  UNL     1      -0.532  -0.310   0.607  1.00  0.00           C  
HETATM    4  C4  UNL     1       0.504   0.380   1.369  1.00  0.00           C  
HETATM    5  C5  UNL     1       1.505   1.184   0.613  1.00  0.00           C  
HETATM    6  C6  UNL     1       2.327   0.367  -0.372  1.00  0.00           C  
HETATM    7  C7  UNL     1       3.312   1.288  -1.109  1.00  0.00           C  
HETATM    8  O1  UNL     1       3.138  -0.549   0.337  1.00  0.00           O  
HETATM    9  C8  UNL     1      -1.579   0.422  -0.128  1.00  0.00           C  
HETATM   10  C9  UNL     1      -1.043   1.511  -1.047  1.00  0.00           C  
HETATM   11  C10 UNL     1      -2.317   1.221   0.992  1.00  0.00           C  
HETATM   12  C11 UNL     1      -2.545  -0.372  -0.912  1.00  0.00           C  
HETATM   13  C12 UNL     1      -2.489  -1.817  -0.829  1.00  0.00           C  
HETATM   14  C13 UNL     1      -1.555  -2.407  -0.107  1.00  0.00           C  
HETATM   15  H1  UNL     1       0.564  -2.137   2.442  1.00  0.00           H  
HETATM   16  H2  UNL     1       0.086  -3.523   1.491  1.00  0.00           H  
HETATM   17  H3  UNL     1       1.380  -2.542   0.829  1.00  0.00           H  
HETATM   18  H4  UNL     1      -0.023   1.134   2.043  1.00  0.00           H  
HETATM   19  H5  UNL     1       1.037  -0.255   2.106  1.00  0.00           H  
HETATM   20  H6  UNL     1       2.316   1.563   1.343  1.00  0.00           H  
HETATM   21  H7  UNL     1       1.154   2.108   0.150  1.00  0.00           H  
HETATM   22  H8  UNL     1       1.733  -0.125  -1.154  1.00  0.00           H  
HETATM   23  H9  UNL     1       2.822   1.729  -2.009  1.00  0.00           H  
HETATM   24  H10 UNL     1       4.123   0.619  -1.472  1.00  0.00           H  
HETATM   25  H11 UNL     1       3.742   2.036  -0.442  1.00  0.00           H  
HETATM   26  H12 UNL     1       3.739  -0.939  -0.361  1.00  0.00           H  
HETATM   27  H13 UNL     1      -1.010   2.507  -0.556  1.00  0.00           H  
HETATM   28  H14 UNL     1      -1.850   1.655  -1.841  1.00  0.00           H  
HETATM   29  H15 UNL     1      -0.148   1.231  -1.603  1.00  0.00           H  
HETATM   30  H16 UNL     1      -2.499   0.556   1.839  1.00  0.00           H  
HETATM   31  H17 UNL     1      -3.281   1.584   0.599  1.00  0.00           H  
HETATM   32  H18 UNL     1      -1.649   2.065   1.229  1.00  0.00           H  
HETATM   33  H19 UNL     1      -2.526  -0.090  -1.995  1.00  0.00           H  
HETATM   34  H20 UNL     1      -3.585  -0.074  -0.566  1.00  0.00           H  
HETATM   35  H21 UNL     1      -3.210  -2.411  -1.357  1.00  0.00           H  
HETATM   36  H22 UNL     1      -1.522  -3.512  -0.052  1.00  0.00           H  
CONECT    1    2   15   16   17
CONECT    2    3    3   14
CONECT    3    4    9
CONECT    4    5   18   19
CONECT    5    6   20   21
CONECT    6    7    8   22
CONECT    7   23   24   25
CONECT    8   26
CONECT    9   10   11   12
CONECT   10   27   28   29
CONECT   11   30   31   32
CONECT   12   13   33   34
CONECT   13   14   14   35
CONECT   14   36
END

HMDB0036184
     RDKit          3D
7,8-Dehydro-3,4-dihydro-beta-ionol
 36 36  0  0  0  0  0  0  0  0999 V2000
    0.4367   -2.4475    1.3992 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5547   -1.6502    0.6278 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5322   -0.3100    0.6072 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5036    0.3796    1.3685 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5053    1.1840    0.6135 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3271    0.3668   -0.3724 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3125    1.2880   -1.1090 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1376   -0.5490    0.3367 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5795    0.4218   -0.1281 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0426    1.5111   -1.0470 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3166    1.2212    0.9918 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5452   -0.3720   -0.9123 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4888   -1.8165   -0.8290 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5553   -2.4066   -0.1072 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5641   -2.1368    2.4418 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0864   -3.5233    1.4907 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3800   -2.5415    0.8285 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0226    1.1342    2.0429 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0368   -0.2554    2.1057 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3159    1.5626    1.3427 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1542    2.1082    0.1502 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7331   -0.1246   -1.1539 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8224    1.7289   -2.0095 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1225    0.6185   -1.4722 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7421    2.0363   -0.4424 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7390   -0.9392   -0.3608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0103    2.5075   -0.5560 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8497    1.6549   -1.8407 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1484    1.2314   -1.6029 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4993    0.5560    1.8390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2807    1.5841    0.5986 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6494    2.0650    1.2292 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5265   -0.0901   -1.9946 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5854   -0.0738   -0.5662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2103   -2.4113   -1.3573 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5217   -3.5122   -0.0522 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  6  8  1  0
  3  9  1  0
  9 10  1  0
  9 11  1  0
  9 12  1  0
 12 13  1  0
 13 14  2  0
 14  2  1  0
  1 15  1  0
  1 16  1  0
  1 17  1  0
  4 18  1  0
  4 19  1  0
  5 20  1  0
  5 21  1  0
  6 22  1  0
  7 23  1  0
  7 24  1  0
  7 25  1  0
  8 26  1  0
 10 27  1  0
 10 28  1  0
 10 29  1  0
 11 30  1  0
 11 31  1  0
 11 32  1  0
 12 33  1  0
 12 34  1  0
 13 35  1  0
 14 36  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
7,8-Dehydro-3,4-dihydro-b-ionol	Generator
7,8-Dehydro-3,4-dihydro-β-ionol	Generator
a,2,6,6-Tetramethyl-1,3-cyclohexadiene-1-propanol, 9ci	HMDB
alpha,2,6,6-Tetramethyl-1,3-cyclohexadiene-1-propanol	HMDB
Dehydrodihydroionol	HMDB
FEMA 3446	HMDB

Chemical Formula

C₁₃H₂₂O

Average Molecular Weight

194.3132

Monoisotopic Molecular Weight

194.167065326

IUPAC Name

4-(2,6,6-trimethylcyclohexa-1,3-dien-1-yl)butan-2-ol

Traditional Name

4-(2,6,6-trimethylcyclohexa-1,3-dien-1-yl)butan-2-ol

CAS Registry Number

57069-86-0

SMILES

CC(O)CCC1=C(C)C=CCC1(C)C

InChI Identifier

InChI=1S/C13H22O/c1-10-6-5-9-13(3,4)12(10)8-7-11(2)14/h5-6,11,14H,7-9H2,1-4H3

InChI Key

WPGXAVCJKGSOBD-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

Megastigmane sesquiterpenoid
Sesquiterpenoid
Secondary alcohol
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Alcohol
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: HMDB0036184)

Source

Endogenous

Endogenous (HMDB: HMDB0036184)

Animal

Animal (HMDB: HMDB0036184)

Exogenous

Food

Food (HMDB: HMDB0036184)

Exogenous (HMDB: HMDB0036184)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid Peroxidation (HMDB: HMDB0036184)

Biochemical pathway

Metabolic pathway

Fatty Acid Metabolism (HMDB: HMDB0036184)

Lipid metabolism pathway (HMDB: HMDB0036184)

Cellular process

Cell signaling (HMDB: HMDB0036184)

Biochemical process

Lipid transport (HMDB: HMDB0036184)

Role

Biological role

Energy source (HMDB: HMDB0036184)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0036184)

Food and nutrition

Food additive

Flavoring agent

Flavoring Agent (HMDB: HMDB0036184)

Physical Properties

State

Not Available

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	80.00 °C. @ 1.00 mm Hg	The Good Scents Company Information System
Water Solubility	16.29 mg/L @ 25 °C (est)	The Good Scents Company Information System
LogP	3.937 (est)	The Good Scents Company Information System

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.39 g/L	ALOGPS
logP	4.29	ALOGPS
logP	2.89	ChemAxon
logS	-2.7	ALOGPS
pKa (Strongest Acidic)	17.72	ChemAxon
pKa (Strongest Basic)	-1.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	20.23 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	62.98 m³·mol⁻¹	ChemAxon
Polarizability	24.02 Å³	ChemAxon
Number of Rings	1	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]+	149.623	31661259
DarkChem	[M-H]-	143.052	31661259
DeepCCS	[M+H]+	149.103	30932474
DeepCCS	[M-H]-	146.708	30932474
DeepCCS	[M-2H]-	182.042	30932474
DeepCCS	[M+Na]+	156.642	30932474
AllCCS	[M+H]+	146.2	32859911
AllCCS	[M+H-H2O]+	142.2	32859911
AllCCS	[M+NH4]+	149.9	32859911
AllCCS	[M+Na]+	151.0	32859911
AllCCS	[M-H]-	151.5	32859911
AllCCS	[M+Na-2H]-	152.6	32859911
AllCCS	[M+HCOO]-	153.9	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
7,8-Dehydro-3,4-dihydro-beta-ionol	CC(O)CCC1=C(C)C=CCC1(C)C	1938.1	Standard polar	33892256
7,8-Dehydro-3,4-dihydro-beta-ionol	CC(O)CCC1=C(C)C=CCC1(C)C	1400.5	Standard non polar	33892256
7,8-Dehydro-3,4-dihydro-beta-ionol	CC(O)CCC1=C(C)C=CCC1(C)C	1429.4	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
7,8-Dehydro-3,4-dihydro-beta-ionol,1TMS,isomer #1	CC1=C(CCC(C)O[Si](C)(C)C)C(C)(C)CC=C1	1610.4	Semi standard non polar	33892256
7,8-Dehydro-3,4-dihydro-beta-ionol,1TBDMS,isomer #1	CC1=C(CCC(C)O[Si](C)(C)C(C)(C)C)C(C)(C)CC=C1	1855.3	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dehydro-3,4-dihydro-beta-ionol GC-MS (Non-derivatized) - 70eV, Positive	splash10-004i-6900000000-fcd19abbee9ae06be131	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dehydro-3,4-dihydro-beta-ionol GC-MS (1 TMS) - 70eV, Positive	splash10-0uki-9750000000-75a710878c65b359d320	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dehydro-3,4-dihydro-beta-ionol GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dehydro-3,4-dihydro-beta-ionol 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 - 7,8-Dehydro-3,4-dihydro-beta-ionol 10V, Positive-QTOF	splash10-004i-1900000000-b61af84b3669e879f2a4	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 7,8-Dehydro-3,4-dihydro-beta-ionol 20V, Positive-QTOF	splash10-004r-4900000000-9c547eee27d57f8787fc	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 7,8-Dehydro-3,4-dihydro-beta-ionol 40V, Positive-QTOF	splash10-0uy0-9700000000-1413f3d2c8942cef4ff3	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 7,8-Dehydro-3,4-dihydro-beta-ionol 10V, Negative-QTOF	splash10-0006-0900000000-2c030a54d3fcb3e8d3ee	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 7,8-Dehydro-3,4-dihydro-beta-ionol 20V, Negative-QTOF	splash10-002f-0900000000-af9acb3a2953d77455c8	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 7,8-Dehydro-3,4-dihydro-beta-ionol 40V, Negative-QTOF	splash10-0a6r-3900000000-8eed5fcd80c5e194de99	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 7,8-Dehydro-3,4-dihydro-beta-ionol 10V, Positive-QTOF	splash10-00g1-1900000000-970bd133541d11424bb4	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 7,8-Dehydro-3,4-dihydro-beta-ionol 20V, Positive-QTOF	splash10-00dr-4900000000-9f938f24750297eb7cfb	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 7,8-Dehydro-3,4-dihydro-beta-ionol 40V, Positive-QTOF	splash10-014i-9500000000-9e717e2f0727bce7da8c	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 7,8-Dehydro-3,4-dihydro-beta-ionol 10V, Negative-QTOF	splash10-0006-0900000000-f4ac9f2710ef63610b81	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 7,8-Dehydro-3,4-dihydro-beta-ionol 20V, Negative-QTOF	splash10-006x-0900000000-0eb4e5226c5116942047	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 7,8-Dehydro-3,4-dihydro-beta-ionol 40V, Negative-QTOF	splash10-0002-1900000000-af6419ab7b2e1e9f4989	2021-09-22	Wishart Lab	View Spectrum

IR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted IR Spectrum	IR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M-H]-)	2023-02-04	FELIX lab	View Spectrum
Predicted IR Spectrum	IR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M+H]+)	2023-02-04	FELIX lab	View Spectrum
Predicted IR Spectrum	IR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M+Na]+)	2023-02-04	FELIX 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

FDB015038

KNApSAcK ID

Not Available

Chemspider ID

55960

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

62126

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

rw1036211

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 7,8-Dehydro-3,4-dihydro-beta-ionol (HMDB0036184)

MOL for HMDB0036184 (7,8-Dehydro-3,4-dihydro-beta-ionol)

3D MOL for HMDB0036184 (7,8-Dehydro-3,4-dihydro-beta-ionol)

3D SDF for HMDB0036184 (7,8-Dehydro-3,4-dihydro-beta-ionol)

3D-SDF for HMDB0036184 (7,8-Dehydro-3,4-dihydro-beta-ionol)

PDB for HMDB0036184 (7,8-Dehydro-3,4-dihydro-beta-ionol)

3D PDB for HMDB0036184 (7,8-Dehydro-3,4-dihydro-beta-ionol)

SMILES for HMDB0036184 (7,8-Dehydro-3,4-dihydro-beta-ionol)

INCHI for HMDB0036184 (7,8-Dehydro-3,4-dihydro-beta-ionol)

Structure for HMDB0036184 (7,8-Dehydro-3,4-dihydro-beta-ionol)

3D Structure for HMDB0036184 (7,8-Dehydro-3,4-dihydro-beta-ionol)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

IR Spectra