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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 21:05:56 UTC

Update Date

2022-03-07 02:54:45 UTC

HMDB ID

HMDB0036032

Secondary Accession Numbers

HMDB36032

Metabolite Identification

Common Name

3beta-7-Drimene-3,11-diol

Description

3beta-7-Drimene-3,11-diol belongs to the class of organic compounds known as cyclic alcohols and derivatives. These are organic compounds containing an aliphatic ring substituted with at least one hydroxyl group. 3beta-7-Drimene-3,11-diol has been detected, but not quantified in, a few different foods, such as common mushrooms (Agaricus bisporus), mushrooms, and oyster mushrooms (Pleurotus ostreatus). This could make 3beta-7-drimene-3,11-diol a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on 3beta-7-Drimene-3,11-diol.

Structure

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

HMDB0036032
     RDKit          3D
3beta-7-Drimene-3,11-diol
 43 44  0  0  0  0  0  0  0  0999 V2000
    3.6769   -1.1104    0.3433 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2200   -1.0567    0.0660 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4483   -2.0517    0.4671 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0026   -1.9422    0.1610 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5454   -0.5784    0.5087 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9822   -0.4548    0.0358 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7832   -1.4152    0.9286 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2027   -0.8771   -1.3672 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4466    0.9187    0.3630 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8017    1.0042    0.0457 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6864    1.9774   -0.3619 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3267    1.5507   -0.8348 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3358    0.5530    0.0853 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8301    1.3445    1.2986 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5810    0.0899   -0.6484 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5963    1.2131   -0.6206 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7840    0.8496   -1.2543 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9105   -1.9265    1.0574 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9890   -0.1680    0.8380 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2742   -1.3315   -0.5716 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8646   -2.9248    1.0061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2139   -2.2422   -0.8892 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5154   -2.7295    0.7848 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6132   -0.5576    1.6190 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6738   -2.4254    0.4737 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3693   -1.4160    1.9599 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8588   -1.1689    0.9084 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7031   -1.8879   -1.4408 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9684   -0.1777   -1.8134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3164   -0.9446   -2.0045 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3345    1.0692    1.4662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3300    0.8286    0.8652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6327    2.9037    0.2386 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2646    2.2657   -1.2891 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3032    2.4890   -0.8098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2928    1.2168   -1.8799 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0316    1.4350    1.9911 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1383    2.3612    1.0368 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6128    0.7794    1.8451 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4064   -0.1688   -1.6965 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8766    1.4942    0.4164 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2651    2.1361   -1.1168 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7781    1.0759   -2.2108 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
  6  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 16 17  1  0
 15  2  1  0
 13  5  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  3 21  1  0
  4 22  1  0
  4 23  1  0
  5 24  1  0
  7 25  1  0
  7 26  1  0
  7 27  1  0
  8 28  1  0
  8 29  1  0
  8 30  1  0
  9 31  1  0
 10 32  1  0
 11 33  1  0
 11 34  1  0
 12 35  1  0
 12 36  1  0
 14 37  1  0
 14 38  1  0
 14 39  1  0
 15 40  1  0
 16 41  1  0
 16 42  1  0
 17 43  1  0
M  END


  Mrv0541 05061308512D          

 17 18  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
    3.0421   -1.0445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1027   -1.0445    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
    1.4289    0.0000    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
    4.2868    0.8250    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    2.0625    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
    2.1434    1.2375    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
    4.2868    0.0000    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
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 O   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
  6  5  1  0  0  0  0
  8  7  1  0  0  0  0
 10  1  1  0  0  0  0
 10  5  2  0  0  0  0
 11  9  1  0  0  0  0
 11 10  1  0  0  0  0
 12  6  1  0  0  0  0
 13  7  1  0  0  0  0
 14  2  1  0  0  0  0
 14  3  1  0  0  0  0
 14 12  1  0  0  0  0
 14 13  1  0  0  0  0
 15  4  1  0  0  0  0
 15  8  1  0  0  0  0
 15 11  1  0  0  0  0
 15 12  1  0  0  0  0
 16  9  1  0  0  0  0
 17 13  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0036032

> <DATABASE_NAME>
hmdb

> <SMILES>
CC1=CCC2C(C)(C)C(O)CCC2(C)C1CO

> <INCHI_IDENTIFIER>
InChI=1S/C15H26O2/c1-10-5-6-12-14(2,3)13(17)7-8-15(12,4)11(10)9-16/h5,11-13,16-17H,6-9H2,1-4H3

> <INCHI_KEY>
SYSFCGLKPBVTDQ-UHFFFAOYSA-N

> <FORMULA>
C15H26O2

> <MOLECULAR_WEIGHT>
238.3657

> <EXACT_MASS>
238.193280076

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_AVERAGE_POLARIZABILITY>
28.24140041207165

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5-(hydroxymethyl)-1,1,4a,6-tetramethyl-1,2,3,4,4a,5,8,8a-octahydronaphthalen-2-ol

> <ALOGPS_LOGP>
2.91

> <JCHEM_LOGP>
2.1328977039999995

> <ALOGPS_LOGS>
-2.82

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
19.554178206614793

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.551144503757758

> <JCHEM_PKA_STRONGEST_BASIC>
-0.6719422619786356

> <JCHEM_POLAR_SURFACE_AREA>
40.46

> <JCHEM_REFRACTIVITY>
70.9162

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.63e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-(hydroxymethyl)-1,1,4a,6-tetramethyl-2,3,4,5,8,8a-hexahydronaphthalen-2-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0036032
     RDKit          3D
3beta-7-Drimene-3,11-diol
 43 44  0  0  0  0  0  0  0  0999 V2000
    3.6769   -1.1104    0.3433 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2200   -1.0567    0.0660 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4483   -2.0517    0.4671 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0026   -1.9422    0.1610 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5454   -0.5784    0.5087 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9822   -0.4548    0.0358 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7832   -1.4152    0.9286 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2027   -0.8771   -1.3672 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4466    0.9187    0.3630 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8017    1.0042    0.0457 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6864    1.9774   -0.3619 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3267    1.5507   -0.8348 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3358    0.5530    0.0853 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8301    1.3445    1.2986 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5810    0.0899   -0.6484 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5963    1.2131   -0.6206 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7840    0.8496   -1.2543 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9105   -1.9265    1.0574 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9890   -0.1680    0.8380 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2742   -1.3315   -0.5716 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8646   -2.9248    1.0061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2139   -2.2422   -0.8892 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5154   -2.7295    0.7848 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6132   -0.5576    1.6190 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6738   -2.4254    0.4737 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3693   -1.4160    1.9599 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8588   -1.1689    0.9084 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7031   -1.8879   -1.4408 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9684   -0.1777   -1.8134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3164   -0.9446   -2.0045 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3345    1.0692    1.4662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3300    0.8286    0.8652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6327    2.9037    0.2386 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2646    2.2657   -1.2891 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3032    2.4890   -0.8098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2928    1.2168   -1.8799 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0316    1.4350    1.9911 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1383    2.3612    1.0368 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6128    0.7794    1.8451 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4064   -0.1688   -1.6965 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8766    1.4942    0.4164 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2651    2.1361   -1.1168 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7781    1.0759   -2.2108 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
  6  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 16 17  1  0
 15  2  1  0
 13  5  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  3 21  1  0
  4 22  1  0
  4 23  1  0
  5 24  1  0
  7 25  1  0
  7 26  1  0
  7 27  1  0
  8 28  1  0
  8 29  1  0
  8 30  1  0
  9 31  1  0
 10 32  1  0
 11 33  1  0
 11 34  1  0
 12 35  1  0
 12 36  1  0
 14 37  1  0
 14 38  1  0
 14 39  1  0
 15 40  1  0
 16 41  1  0
 16 42  1  0
 17 43  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       5.679  -1.950   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.658  -1.950   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.335   3.080   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.002   1.540   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   3.850   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.335   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       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       5.335   4.620   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       9.336  -0.770   0.000  0.00  0.00           O+0
CONECT    1   10                                                            
CONECT    2   14                                                            
CONECT    3   14                                                            
CONECT    4   15                                                            
CONECT    5    6   10                                                       
CONECT    6    5   12                                                       
CONECT    7    8   13                                                       
CONECT    8    7   15                                                       
CONECT    9   11   16                                                       
CONECT   10    1    5   11                                                  
CONECT   11    9   10   15                                                  
CONECT   12    6   14   15                                                  
CONECT   13    7   14   17                                                  
CONECT   14    2    3   12   13                                             
CONECT   15    4    8   11   12                                             
CONECT   16    9                                                            
CONECT   17   13                                                            
MASTER        0    0    0    0    0    0    0    0   17    0   36    0
END

COMPND    HMDB0036032
HETATM    1  C1  UNL     1       3.677  -1.110   0.343  1.00  0.00           C  
HETATM    2  C2  UNL     1       2.220  -1.057   0.066  1.00  0.00           C  
HETATM    3  C3  UNL     1       1.448  -2.052   0.467  1.00  0.00           C  
HETATM    4  C4  UNL     1       0.003  -1.942   0.161  1.00  0.00           C  
HETATM    5  C5  UNL     1      -0.545  -0.578   0.509  1.00  0.00           C  
HETATM    6  C6  UNL     1      -1.982  -0.455   0.036  1.00  0.00           C  
HETATM    7  C7  UNL     1      -2.783  -1.415   0.929  1.00  0.00           C  
HETATM    8  C8  UNL     1      -2.203  -0.877  -1.367  1.00  0.00           C  
HETATM    9  C9  UNL     1      -2.447   0.919   0.363  1.00  0.00           C  
HETATM   10  O1  UNL     1      -3.802   1.004   0.046  1.00  0.00           O  
HETATM   11  C10 UNL     1      -1.686   1.977  -0.362  1.00  0.00           C  
HETATM   12  C11 UNL     1      -0.327   1.551  -0.835  1.00  0.00           C  
HETATM   13  C12 UNL     1       0.336   0.553   0.085  1.00  0.00           C  
HETATM   14  C13 UNL     1       0.830   1.344   1.299  1.00  0.00           C  
HETATM   15  C14 UNL     1       1.581   0.090  -0.648  1.00  0.00           C  
HETATM   16  C15 UNL     1       2.596   1.213  -0.621  1.00  0.00           C  
HETATM   17  O2  UNL     1       3.784   0.850  -1.254  1.00  0.00           O  
HETATM   18  H1  UNL     1       3.910  -1.926   1.057  1.00  0.00           H  
HETATM   19  H2  UNL     1       3.989  -0.168   0.838  1.00  0.00           H  
HETATM   20  H3  UNL     1       4.274  -1.331  -0.572  1.00  0.00           H  
HETATM   21  H4  UNL     1       1.865  -2.925   1.006  1.00  0.00           H  
HETATM   22  H5  UNL     1      -0.214  -2.242  -0.889  1.00  0.00           H  
HETATM   23  H6  UNL     1      -0.515  -2.729   0.785  1.00  0.00           H  
HETATM   24  H7  UNL     1      -0.613  -0.558   1.619  1.00  0.00           H  
HETATM   25  H8  UNL     1      -2.674  -2.425   0.474  1.00  0.00           H  
HETATM   26  H9  UNL     1      -2.369  -1.416   1.960  1.00  0.00           H  
HETATM   27  H10 UNL     1      -3.859  -1.169   0.908  1.00  0.00           H  
HETATM   28  H11 UNL     1      -2.703  -1.888  -1.441  1.00  0.00           H  
HETATM   29  H12 UNL     1      -2.968  -0.178  -1.813  1.00  0.00           H  
HETATM   30  H13 UNL     1      -1.316  -0.945  -2.004  1.00  0.00           H  
HETATM   31  H14 UNL     1      -2.335   1.069   1.466  1.00  0.00           H  
HETATM   32  H15 UNL     1      -4.330   0.829   0.865  1.00  0.00           H  
HETATM   33  H16 UNL     1      -1.633   2.904   0.239  1.00  0.00           H  
HETATM   34  H17 UNL     1      -2.265   2.266  -1.289  1.00  0.00           H  
HETATM   35  H18 UNL     1       0.303   2.489  -0.810  1.00  0.00           H  
HETATM   36  H19 UNL     1      -0.293   1.217  -1.880  1.00  0.00           H  
HETATM   37  H20 UNL     1      -0.032   1.435   1.991  1.00  0.00           H  
HETATM   38  H21 UNL     1       1.138   2.361   1.037  1.00  0.00           H  
HETATM   39  H22 UNL     1       1.613   0.779   1.845  1.00  0.00           H  
HETATM   40  H23 UNL     1       1.406  -0.169  -1.697  1.00  0.00           H  
HETATM   41  H24 UNL     1       2.877   1.494   0.416  1.00  0.00           H  
HETATM   42  H25 UNL     1       2.265   2.136  -1.117  1.00  0.00           H  
HETATM   43  H26 UNL     1       3.778   1.076  -2.211  1.00  0.00           H  
CONECT    1    2   18   19   20
CONECT    2    3    3   15
CONECT    3    4   21
CONECT    4    5   22   23
CONECT    5    6   13   24
CONECT    6    7    8    9
CONECT    7   25   26   27
CONECT    8   28   29   30
CONECT    9   10   11   31
CONECT   10   32
CONECT   11   12   33   34
CONECT   12   13   35   36
CONECT   13   14   15
CONECT   14   37   38   39
CONECT   15   16   40
CONECT   16   17   41   42
CONECT   17   43
END

HMDB0036032
     RDKit          3D
3beta-7-Drimene-3,11-diol
 43 44  0  0  0  0  0  0  0  0999 V2000
    3.6769   -1.1104    0.3433 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2200   -1.0567    0.0660 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4483   -2.0517    0.4671 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0026   -1.9422    0.1610 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5454   -0.5784    0.5087 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9822   -0.4548    0.0358 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7832   -1.4152    0.9286 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2027   -0.8771   -1.3672 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4466    0.9187    0.3630 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8017    1.0042    0.0457 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6864    1.9774   -0.3619 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3267    1.5507   -0.8348 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3358    0.5530    0.0853 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8301    1.3445    1.2986 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5810    0.0899   -0.6484 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5963    1.2131   -0.6206 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7840    0.8496   -1.2543 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9105   -1.9265    1.0574 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9890   -0.1680    0.8380 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2742   -1.3315   -0.5716 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8646   -2.9248    1.0061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2139   -2.2422   -0.8892 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5154   -2.7295    0.7848 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6132   -0.5576    1.6190 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6738   -2.4254    0.4737 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3693   -1.4160    1.9599 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8588   -1.1689    0.9084 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7031   -1.8879   -1.4408 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9684   -0.1777   -1.8134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3164   -0.9446   -2.0045 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3345    1.0692    1.4662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3300    0.8286    0.8652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6327    2.9037    0.2386 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2646    2.2657   -1.2891 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3032    2.4890   -0.8098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2928    1.2168   -1.8799 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0316    1.4350    1.9911 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1383    2.3612    1.0368 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6128    0.7794    1.8451 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4064   -0.1688   -1.6965 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8766    1.4942    0.4164 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2651    2.1361   -1.1168 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7781    1.0759   -2.2108 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
  6  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 16 17  1  0
 15  2  1  0
 13  5  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  3 21  1  0
  4 22  1  0
  4 23  1  0
  5 24  1  0
  7 25  1  0
  7 26  1  0
  7 27  1  0
  8 28  1  0
  8 29  1  0
  8 30  1  0
  9 31  1  0
 10 32  1  0
 11 33  1  0
 11 34  1  0
 12 35  1  0
 12 36  1  0
 14 37  1  0
 14 38  1  0
 14 39  1  0
 15 40  1  0
 16 41  1  0
 16 42  1  0
 17 43  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
3b-7-Drimene-3,11-diol	Generator
3Β-7-drimene-3,11-diol	Generator

Chemical Formula

C₁₅H₂₆O₂

Average Molecular Weight

238.3657

Monoisotopic Molecular Weight

238.193280076

IUPAC Name

5-(hydroxymethyl)-1,1,4a,6-tetramethyl-1,2,3,4,4a,5,8,8a-octahydronaphthalen-2-ol

Traditional Name

5-(hydroxymethyl)-1,1,4a,6-tetramethyl-2,3,4,5,8,8a-hexahydronaphthalen-2-ol

CAS Registry Number

Not Available

SMILES

CC1=CCC2C(C)(C)C(O)CCC2(C)C1CO

InChI Identifier

InChI=1S/C15H26O2/c1-10-5-6-12-14(2,3)13(17)7-8-15(12,4)11(10)9-16/h5,11-13,16-17H,6-9H2,1-4H3

InChI Key

SYSFCGLKPBVTDQ-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cyclic alcohols and derivatives. These are organic compounds containing an aliphatic ring substituted with at least one hydroxyl group.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Alcohols and polyols

Direct Parent

Cyclic alcohols and derivatives

Alternative Parents

Substituents

Cyclic alcohol
Secondary alcohol
Hydrocarbon derivative
Primary alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Route of exposure

Enteral

Ingestion (HMDB: HMDB0036032)

Source

Endogenous

Endogenous (HMDB: HMDB0036032)

Plant

Plant (HMDB: HMDB0036032)

Exogenous

Food

Food (HMDB: HMDB0036032)

Vegetable

Mushroom

Exogenous (HMDB: HMDB0036032)

Process

Naturally occurring process

Biological process

Cellular process

Cell signaling (HMDB: HMDB0036032)

Role

Biological role

Energy source (HMDB: HMDB0036032)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0036032)

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	0.36 g/L	ALOGPS
logP	2.91	ALOGPS
logP	2.13	ChemAxon
logS	-2.8	ALOGPS
pKa (Strongest Acidic)	18.55	ChemAxon
pKa (Strongest Basic)	-0.67	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	1	ChemAxon
Refractivity	70.92 m³·mol⁻¹	ChemAxon
Polarizability	28.24 Å³	ChemAxon
Number of Rings	2	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]+	155.387	31661259
DarkChem	[M-H]-	154.142	31661259
DeepCCS	[M+H]+	155.797	30932474
DeepCCS	[M-H]-	153.439	30932474
DeepCCS	[M-2H]-	186.669	30932474
DeepCCS	[M+Na]+	161.89	30932474
AllCCS	[M+H]+	156.9	32859911
AllCCS	[M+H-H2O]+	153.2	32859911
AllCCS	[M+NH4]+	160.2	32859911
AllCCS	[M+Na]+	161.2	32859911
AllCCS	[M-H]-	163.4	32859911
AllCCS	[M+Na-2H]-	164.0	32859911
AllCCS	[M+HCOO]-	164.8	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.	4.62 minutes	32390414
Predicted by Siyang on May 30, 2022	11.4325 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	2.11 minutes	32390414
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	2014.4 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	247.6 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	155.8 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	161.9 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	121.0 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	429.2 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	497.3 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	69.8 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	877.0 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	388.1 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	1134.6 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	318.7 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	354.4 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	273.2 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	253.0 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	11.8 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
3beta-7-Drimene-3,11-diol	CC1=CCC2C(C)(C)C(O)CCC2(C)C1CO	2865.1	Standard polar	33892256
3beta-7-Drimene-3,11-diol	CC1=CCC2C(C)(C)C(O)CCC2(C)C1CO	1852.6	Standard non polar	33892256
3beta-7-Drimene-3,11-diol	CC1=CCC2C(C)(C)C(O)CCC2(C)C1CO	1992.3	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
3beta-7-Drimene-3,11-diol,1TMS,isomer #1	CC1=CCC2C(C)(C)C(O[Si](C)(C)C)CCC2(C)C1CO	1949.5	Semi standard non polar	33892256
3beta-7-Drimene-3,11-diol,1TMS,isomer #2	CC1=CCC2C(C)(C)C(O)CCC2(C)C1CO[Si](C)(C)C	2005.5	Semi standard non polar	33892256
3beta-7-Drimene-3,11-diol,2TMS,isomer #1	CC1=CCC2C(C)(C)C(O[Si](C)(C)C)CCC2(C)C1CO[Si](C)(C)C	1977.7	Semi standard non polar	33892256
3beta-7-Drimene-3,11-diol,1TBDMS,isomer #1	CC1=CCC2C(C)(C)C(O[Si](C)(C)C(C)(C)C)CCC2(C)C1CO	2192.5	Semi standard non polar	33892256
3beta-7-Drimene-3,11-diol,1TBDMS,isomer #2	CC1=CCC2C(C)(C)C(O)CCC2(C)C1CO[Si](C)(C)C(C)(C)C	2277.6	Semi standard non polar	33892256
3beta-7-Drimene-3,11-diol,2TBDMS,isomer #1	CC1=CCC2C(C)(C)C(O[Si](C)(C)C(C)(C)C)CCC2(C)C1CO[Si](C)(C)C(C)(C)C	2477.8	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 - 3beta-7-Drimene-3,11-diol GC-MS (Non-derivatized) - 70eV, Positive	splash10-0kg9-0960000000-53cf9a4e190a290ea998	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3beta-7-Drimene-3,11-diol GC-MS (2 TMS) - 70eV, Positive	splash10-016r-3197000000-22396e2686be6bb538e7	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3beta-7-Drimene-3,11-diol GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3beta-7-Drimene-3,11-diol 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 - 3beta-7-Drimene-3,11-diol 10V, Positive-QTOF	splash10-00dr-0090000000-b33d4d4b7d7a9f3be256	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3beta-7-Drimene-3,11-diol 20V, Positive-QTOF	splash10-0fk9-1690000000-1073877a9a0e7601aa5e	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3beta-7-Drimene-3,11-diol 40V, Positive-QTOF	splash10-00kg-5900000000-15bba91bf9539acb64f1	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3beta-7-Drimene-3,11-diol 10V, Negative-QTOF	splash10-000i-0090000000-107968e2091f659a025c	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3beta-7-Drimene-3,11-diol 20V, Negative-QTOF	splash10-00kr-0190000000-3f86e7e2c955365fd429	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3beta-7-Drimene-3,11-diol 40V, Negative-QTOF	splash10-052o-2950000000-f0b618a876aa528b769a	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3beta-7-Drimene-3,11-diol 10V, Positive-QTOF	splash10-0fe0-0190000000-1729fb4159246af29bde	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3beta-7-Drimene-3,11-diol 20V, Positive-QTOF	splash10-0080-3940000000-af04a042dcc02b1e5cd1	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3beta-7-Drimene-3,11-diol 40V, Positive-QTOF	splash10-001l-9300000000-41d9add9c274ae7c85ee	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3beta-7-Drimene-3,11-diol 10V, Negative-QTOF	splash10-000i-0090000000-e665f494a7390ebf108d	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3beta-7-Drimene-3,11-diol 20V, Negative-QTOF	splash10-000i-0090000000-3ce935a8b850f78c307c	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3beta-7-Drimene-3,11-diol 40V, Negative-QTOF	splash10-0a4i-0190000000-8b0f374b8961fcdef12d	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

FDB014851

KNApSAcK ID

Not Available

Chemspider ID

35014069

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

14433088

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

(). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .

Showing metabocard for 3beta-7-Drimene-3,11-diol (HMDB0036032)

MOL for HMDB0036032 (3beta-7-Drimene-3,11-diol)

3D MOL for HMDB0036032 (3beta-7-Drimene-3,11-diol)

3D SDF for HMDB0036032 (3beta-7-Drimene-3,11-diol)

3D-SDF for HMDB0036032 (3beta-7-Drimene-3,11-diol)

PDB for HMDB0036032 (3beta-7-Drimene-3,11-diol)

3D PDB for HMDB0036032 (3beta-7-Drimene-3,11-diol)

SMILES for HMDB0036032 (3beta-7-Drimene-3,11-diol)

INCHI for HMDB0036032 (3beta-7-Drimene-3,11-diol)

Structure for HMDB0036032 (3beta-7-Drimene-3,11-diol)

3D Structure for HMDB0036032 (3beta-7-Drimene-3,11-diol)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra