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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2021-09-23 18:02:39 UTC

Update Date

2021-09-23 18:02:39 UTC

HMDB ID

HMDB0302472

Secondary Accession Numbers

None

Metabolite Identification

Common Name

2,6-Dimethylocta-cis-2,7-diene-1,6-diol

Description

2,6-dimethylocta-cis-2,7-diene-1,6-diol is a member of the class of compounds known as acyclic monoterpenoids. Acyclic monoterpenoids are monoterpenes that do not contain a cycle. 2,6-dimethylocta-cis-2,7-diene-1,6-diol is slightly soluble (in water) and an extremely weak acidic compound (based on its pKa). 2,6-dimethylocta-cis-2,7-diene-1,6-diol can be found in papaya, which makes 2,6-dimethylocta-cis-2,7-diene-1,6-diol a potential biomarker for the consumption of this food product.

Structure

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

HMDB0302472
     RDKit          3D
2,6-Dimethylocta-cis-2,7-diene-1,6-diol
 30 29  0  0  0  0  0  0  0  0999 V2000
    2.4922    1.6165   -1.1125 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4916    0.3027   -0.9792 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2826   -0.3254    0.3187 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1177   -1.5895    0.5061 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6972    0.5614    1.3113 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8514   -0.7181    0.5836 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0858    0.4814    0.5485 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4390   -0.0572    0.8230 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4736    0.0261    0.0203 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7633   -0.5792    0.4698 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4228    0.6855   -1.2954 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3643    1.7448   -1.2788 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6479    2.1110   -2.0821 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3400    2.3054   -0.2814 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6498   -0.3034   -1.8543 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6217   -2.4601    0.0220 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1574   -1.4433    0.2116 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0746   -1.8064    1.6069 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0226    0.0847    2.1172 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4735   -1.4382   -0.1686 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7765   -1.1490    1.6022 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0068    0.9823   -0.4077 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1457    1.1780    1.4025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5863   -0.5807    1.8036 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5869   -1.3098    1.2671 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2767   -1.1118   -0.3654 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4606    0.1840    0.8655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7854   -0.0384   -2.0882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4859    1.1342   -1.5906 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1188    1.5126   -0.6612 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  1  0
  3  5  1  0
  3  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
  1 13  1  0
  1 14  1  0
  2 15  1  0
  4 16  1  0
  4 17  1  0
  4 18  1  0
  5 19  1  0
  6 20  1  0
  6 21  1  0
  7 22  1  0
  7 23  1  0
  8 24  1  0
 10 25  1  0
 10 26  1  0
 10 27  1  0
 11 28  1  0
 11 29  1  0
 12 30  1  0
M  END

Linalool (cis-8-hydroxy-)
  Mrv1572001071617082D          
  Mrv0541 01101311042D          
 14 13  0  0  0  0            999 V2000
    0.9715   -0.2406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6860    0.1719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2735    0.8864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4485    0.8864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0360    1.6008    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7890    1.6008    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2015    0.8864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2015    2.3153    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0985   -0.5426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9235   -0.5426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7890    0.1719    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4005    0.5844    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1149    0.1719    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2015   -0.5426    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  2  9  1  0  0  0  0
  9 10  2  0  0  0  0
  7 11  1  0  0  0  0
  2 12  1  0  0  0  0
 12 13  1  0  0  0  0
 11 14  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0302472

> <DATABASE_NAME>
hmdb

> <SMILES>
[H]OC\C(C)=C/CCC(C)(O[H])C=C

> <INCHI_IDENTIFIER>
InChI=1S/C10H18O2/c1-4-10(3,12)7-5-6-9(2)8-11/h4,6,11-12H,1,5,7-8H2,2-3H3/b9-6-

> <INCHI_KEY>
NSMIMJYEKVSYMT-TWGQIWQCSA-N

> <FORMULA>
C10H18O2

> <MOLECULAR_WEIGHT>
170.252

> <EXACT_MASS>
170.13067982

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
30

> <JCHEM_AVERAGE_POLARIZABILITY>
20.158161716236336

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2Z)-2,6-dimethylocta-2,7-diene-1,6-diol

> <ALOGPS_LOGP>
1.35

> <JCHEM_LOGP>
1.3667212959999993

> <ALOGPS_LOGS>
-1.57

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
18.45938795806991

> <JCHEM_PKA_STRONGEST_ACIDIC>
16.644023096128976

> <JCHEM_PKA_STRONGEST_BASIC>
-1.2856637071402215

> <JCHEM_POLAR_SURFACE_AREA>
40.46

> <JCHEM_REFRACTIVITY>
51.981300000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.55e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2Z)-2,6-dimethylocta-2,7-diene-1,6-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0302472
     RDKit          3D
2,6-Dimethylocta-cis-2,7-diene-1,6-diol
 30 29  0  0  0  0  0  0  0  0999 V2000
    2.4922    1.6165   -1.1125 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4916    0.3027   -0.9792 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2826   -0.3254    0.3187 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1177   -1.5895    0.5061 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6972    0.5614    1.3113 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8514   -0.7181    0.5836 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0858    0.4814    0.5485 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4390   -0.0572    0.8230 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4736    0.0261    0.0203 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7633   -0.5792    0.4698 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4228    0.6855   -1.2954 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3643    1.7448   -1.2788 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6479    2.1110   -2.0821 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3400    2.3054   -0.2814 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6498   -0.3034   -1.8543 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6217   -2.4601    0.0220 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1574   -1.4433    0.2116 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0746   -1.8064    1.6069 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0226    0.0847    2.1172 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4735   -1.4382   -0.1686 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7765   -1.1490    1.6022 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0068    0.9823   -0.4077 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1457    1.1780    1.4025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5863   -0.5807    1.8036 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5869   -1.3098    1.2671 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2767   -1.1118   -0.3654 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4606    0.1840    0.8655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7854   -0.0384   -2.0882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4859    1.1342   -1.5906 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1188    1.5126   -0.6612 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  1  0
  3  5  1  0
  3  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
  1 13  1  0
  1 14  1  0
  2 15  1  0
  4 16  1  0
  4 17  1  0
  4 18  1  0
  5 19  1  0
  6 20  1  0
  6 21  1  0
  7 22  1  0
  7 23  1  0
  8 24  1  0
 10 25  1  0
 10 26  1  0
 10 27  1  0
 11 28  1  0
 11 29  1  0
 12 30  1  0
M  END

HEADER    PROTEIN                                 07-JAN-16   NONE
TITLE     NULL                                                        
COMPND    MOLECULE: Linalool (cis-8-hydroxy-)                         
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-JAN-16         0                                  
HETATM    1  C   UNK     0       1.813  -0.449   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.147   0.321   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.377   1.655   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.837   1.655   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.067   2.988   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.473   2.988   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.243   1.655   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.243   4.322   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.917  -1.013   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.457  -1.013   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -1.473   0.321   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0       4.481   1.091   0.000  0.00  0.00           O+0
HETATM   13  H   UNK     0       5.814   0.321   0.000  0.00  0.00           H+0
HETATM   14  H   UNK     0      -2.243  -1.013   0.000  0.00  0.00           H+0
CONECT    1    2                                                            
CONECT    2    1    3    9   12                                             
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6   11                                                       
CONECT    8    6                                                            
CONECT    9    2   10                                                       
CONECT   10    9                                                            
CONECT   11    7   14                                                       
CONECT   12    2   13                                                       
CONECT   13   12                                                            
CONECT   14   11                                                            
MASTER        0    0    0    0    0    0    0    0   14    0   26    0
END

COMPND    HMDB0302472
HETATM    1  C1  UNL     1       2.492   1.616  -1.113  1.00  0.00           C  
HETATM    2  C2  UNL     1       2.492   0.303  -0.979  1.00  0.00           C  
HETATM    3  C3  UNL     1       2.283  -0.325   0.319  1.00  0.00           C  
HETATM    4  C4  UNL     1       3.118  -1.589   0.506  1.00  0.00           C  
HETATM    5  O1  UNL     1       2.697   0.561   1.311  1.00  0.00           O  
HETATM    6  C5  UNL     1       0.851  -0.718   0.584  1.00  0.00           C  
HETATM    7  C6  UNL     1      -0.086   0.481   0.549  1.00  0.00           C  
HETATM    8  C7  UNL     1      -1.439  -0.057   0.823  1.00  0.00           C  
HETATM    9  C8  UNL     1      -2.474   0.026   0.020  1.00  0.00           C  
HETATM   10  C9  UNL     1      -3.763  -0.579   0.470  1.00  0.00           C  
HETATM   11  C10 UNL     1      -2.423   0.685  -1.295  1.00  0.00           C  
HETATM   12  O2  UNL     1      -3.364   1.745  -1.279  1.00  0.00           O  
HETATM   13  H1  UNL     1       2.648   2.111  -2.082  1.00  0.00           H  
HETATM   14  H2  UNL     1       2.340   2.305  -0.281  1.00  0.00           H  
HETATM   15  H3  UNL     1       2.650  -0.303  -1.854  1.00  0.00           H  
HETATM   16  H4  UNL     1       2.622  -2.460   0.022  1.00  0.00           H  
HETATM   17  H5  UNL     1       4.157  -1.443   0.212  1.00  0.00           H  
HETATM   18  H6  UNL     1       3.075  -1.806   1.607  1.00  0.00           H  
HETATM   19  H7  UNL     1       3.023   0.085   2.117  1.00  0.00           H  
HETATM   20  H8  UNL     1       0.474  -1.438  -0.169  1.00  0.00           H  
HETATM   21  H9  UNL     1       0.777  -1.149   1.602  1.00  0.00           H  
HETATM   22  H10 UNL     1       0.007   0.982  -0.408  1.00  0.00           H  
HETATM   23  H11 UNL     1       0.146   1.178   1.403  1.00  0.00           H  
HETATM   24  H12 UNL     1      -1.586  -0.581   1.804  1.00  0.00           H  
HETATM   25  H13 UNL     1      -3.587  -1.310   1.267  1.00  0.00           H  
HETATM   26  H14 UNL     1      -4.277  -1.112  -0.365  1.00  0.00           H  
HETATM   27  H15 UNL     1      -4.461   0.184   0.866  1.00  0.00           H  
HETATM   28  H16 UNL     1      -2.785  -0.038  -2.088  1.00  0.00           H  
HETATM   29  H17 UNL     1      -1.486   1.134  -1.591  1.00  0.00           H  
HETATM   30  H18 UNL     1      -4.119   1.513  -0.661  1.00  0.00           H  
CONECT    1    2    2   13   14
CONECT    2    3   15
CONECT    3    4    5    6
CONECT    4   16   17   18
CONECT    5   19
CONECT    6    7   20   21
CONECT    7    8   22   23
CONECT    8    9    9   24
CONECT    9   10   11
CONECT   10   25   26   27
CONECT   11   12   28   29
CONECT   12   30
END

HMDB0302472
     RDKit          3D
2,6-Dimethylocta-cis-2,7-diene-1,6-diol
 30 29  0  0  0  0  0  0  0  0999 V2000
    2.4922    1.6165   -1.1125 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4916    0.3027   -0.9792 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2826   -0.3254    0.3187 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1177   -1.5895    0.5061 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6972    0.5614    1.3113 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8514   -0.7181    0.5836 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0858    0.4814    0.5485 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4390   -0.0572    0.8230 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4736    0.0261    0.0203 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7633   -0.5792    0.4698 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4228    0.6855   -1.2954 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3643    1.7448   -1.2788 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6479    2.1110   -2.0821 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3400    2.3054   -0.2814 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6498   -0.3034   -1.8543 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6217   -2.4601    0.0220 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1574   -1.4433    0.2116 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0746   -1.8064    1.6069 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0226    0.0847    2.1172 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4735   -1.4382   -0.1686 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7765   -1.1490    1.6022 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0068    0.9823   -0.4077 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1457    1.1780    1.4025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5863   -0.5807    1.8036 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5869   -1.3098    1.2671 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2767   -1.1118   -0.3654 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4606    0.1840    0.8655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7854   -0.0384   -2.0882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4859    1.1342   -1.5906 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1188    1.5126   -0.6612 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  1  0
  3  5  1  0
  3  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
  1 13  1  0
  1 14  1  0
  2 15  1  0
  4 16  1  0
  4 17  1  0
  4 18  1  0
  5 19  1  0
  6 20  1  0
  6 21  1  0
  7 22  1  0
  7 23  1  0
  8 24  1  0
 10 25  1  0
 10 26  1  0
 10 27  1  0
 11 28  1  0
 11 29  1  0
 12 30  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₁₀H₁₈O₂

Average Molecular Weight

170.252

Monoisotopic Molecular Weight

170.13067982

IUPAC Name

(2Z)-2,6-dimethylocta-2,7-diene-1,6-diol

Traditional Name

(2Z)-2,6-dimethylocta-2,7-diene-1,6-diol

CAS Registry Number

Not Available

SMILES

[H]OC\C(C)=C/CCC(C)(O[H])C=C

InChI Identifier

InChI=1S/C10H18O2/c1-4-10(3,12)7-5-6-9(2)8-11/h4,6,11-12H,1,5,7-8H2,2-3H3/b9-6-

InChI Key

NSMIMJYEKVSYMT-TWGQIWQCSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as acyclic monoterpenoids. These are monoterpenes that do not contain a cycle.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Monoterpenoids

Direct Parent

Acyclic monoterpenoids

Alternative Parents

Substituents

Acyclic monoterpenoid
Fatty alcohol
Fatty acyl
Tertiary alcohol
Organic oxygen compound
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Alcohol
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Not Available

Ontology

Not Available

Grape (FooDB: FOOD00369)

Tropical fruit

Papaya (FooDB: FOOD00041)

Beverage

Fermented beverage

Grape wine (FooDB: FOOD00612)

Process

Not Available

Role

Not Available

Physical Properties

State

Not Available

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	1.35	ALOGPS
logP	1.37	ChemAxon
logS	-1.6	ALOGPS
pKa (Strongest Acidic)	16.64	ChemAxon
pKa (Strongest Basic)	-1.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	40.46 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	51.98 m³·mol⁻¹	ChemAxon
Polarizability	20.16 Å³	ChemAxon
Number of Rings	0	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
AllCCS	[M+H]+	141.894	32859911
AllCCS	[M+H-H2O]+	137.95	32859911
AllCCS	[M+Na]+	146.625	32859911
AllCCS	[M+NH4]+	145.567	32859911
AllCCS	[M-H]-	141.231	32859911
AllCCS	[M+Na-2H]-	142.986	32859911
AllCCS	[M+HCOO]-	144.992	32859911
DeepCCS	[M+H]+	145.181	30932474
DeepCCS	[M-H]-	142.823	30932474
DeepCCS	[M-2H]-	177.507	30932474
DeepCCS	[M+Na]+	152.277	30932474

Predicted Kovats Retention Indices

Not Available

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 2,6-Dimethylocta-cis-2,7-diene-1,6-diol GC-MS (Non-derivatized) - 70eV, Positive	splash10-0g3c-9200000000-d0357a65c329fd0e657a	2017-07-27	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 - 2,6-Dimethylocta-cis-2,7-diene-1,6-diol 10V, Positive-QTOF	splash10-0uk9-1900000000-fbec4bc7f37fb339dd6f	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,6-Dimethylocta-cis-2,7-diene-1,6-diol 20V, Positive-QTOF	splash10-0f79-8900000000-64907bf286d3eb52bf39	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,6-Dimethylocta-cis-2,7-diene-1,6-diol 40V, Positive-QTOF	splash10-0uxr-9100000000-6ac0671fb6f272fe55a8	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,6-Dimethylocta-cis-2,7-diene-1,6-diol 10V, Negative-QTOF	splash10-014i-0900000000-c912c14b4e6c2aebea13	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,6-Dimethylocta-cis-2,7-diene-1,6-diol 20V, Negative-QTOF	splash10-0gb9-1900000000-bada202deddb87e761e3	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,6-Dimethylocta-cis-2,7-diene-1,6-diol 40V, Negative-QTOF	splash10-0609-9500000000-9037add03874b04e7c0b	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,6-Dimethylocta-cis-2,7-diene-1,6-diol 10V, Positive-QTOF	splash10-00ls-9200000000-0ca6939d3a29f53bb4dd	2021-10-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,6-Dimethylocta-cis-2,7-diene-1,6-diol 20V, Positive-QTOF	splash10-014i-9000000000-2517b5de9861c13d447a	2021-10-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,6-Dimethylocta-cis-2,7-diene-1,6-diol 40V, Positive-QTOF	splash10-00pl-9000000000-bbe00c04a6d9739f9039	2021-10-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,6-Dimethylocta-cis-2,7-diene-1,6-diol 10V, Negative-QTOF	splash10-014i-0900000000-e5fc112e9b69c0696e8b	2021-10-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,6-Dimethylocta-cis-2,7-diene-1,6-diol 20V, Negative-QTOF	splash10-0gi0-3900000000-287ec52990085c63da8f	2021-10-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,6-Dimethylocta-cis-2,7-diene-1,6-diol 40V, Negative-QTOF	splash10-0uka-9200000000-e488d87bbb2819a1f650	2021-10-21	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

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

FDB004695

KNApSAcK ID

Not Available

Chemspider ID

4509334

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5352452

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

Not Available

Showing metabocard for 2,6-Dimethylocta-cis-2,7-diene-1,6-diol (HMDB0302472)

MOL for HMDB0302472 (2,6-Dimethylocta-cis-2,7-diene-1,6-diol)

3D MOL for HMDB0302472 (2,6-Dimethylocta-cis-2,7-diene-1,6-diol)

3D SDF for HMDB0302472 (2,6-Dimethylocta-cis-2,7-diene-1,6-diol)

3D-SDF for HMDB0302472 (2,6-Dimethylocta-cis-2,7-diene-1,6-diol)

PDB for HMDB0302472 (2,6-Dimethylocta-cis-2,7-diene-1,6-diol)

3D PDB for HMDB0302472 (2,6-Dimethylocta-cis-2,7-diene-1,6-diol)

SMILES for HMDB0302472 (2,6-Dimethylocta-cis-2,7-diene-1,6-diol)

INCHI for HMDB0302472 (2,6-Dimethylocta-cis-2,7-diene-1,6-diol)

Structure for HMDB0302472 (2,6-Dimethylocta-cis-2,7-diene-1,6-diol)

3D Structure for HMDB0302472 (2,6-Dimethylocta-cis-2,7-diene-1,6-diol)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

GC-MS Spectra

MS/MS Spectra