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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 21:51:03 UTC

Update Date

2022-03-07 02:55:01 UTC

HMDB ID

HMDB0036684

Secondary Accession Numbers

HMDB36684

Metabolite Identification

Common Name

2,4,5,7alpha-Tetrahydro-1,4,4,7a-tetramethyl-1H-inden-2-ol

Description

2,4,5,7alpha-Tetrahydro-1,4,4,7a-tetramethyl-1H-inden-2-ol belongs to the class of organic compounds known as secondary alcohols. Secondary alcohols are compounds containing a secondary alcohol functional group, with the general structure HOC(R)(R') (R,R'=alkyl, aryl). 2,4,5,7alpha-Tetrahydro-1,4,4,7a-tetramethyl-1H-inden-2-ol has been detected, but not quantified in, fruits and quinces (Cydonia oblonga). This could make 2,4,5,7alpha-tetrahydro-1,4,4,7a-tetramethyl-1H-inden-2-ol a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on 2,4,5,7alpha-Tetrahydro-1,4,4,7a-tetramethyl-1H-inden-2-ol.

Structure

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

HMDB0036684
     RDKit          3D
2,4,5,7alpha-Tetrahydro-1,4,4,7a-tetramethyl-1H-inden-2-ol
 34 35  0  0  0  0  0  0  0  0999 V2000
   -2.3791   -0.4056    1.4709 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0598   -0.0497    0.0432 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8726   -1.2706   -0.8270 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4519   -2.3593   -0.1581 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4150   -1.4771   -0.8057 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2315   -0.4045   -0.3941 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6976   -0.1040   -0.1975 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5054   -0.4995   -1.4044 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2492   -0.8898    0.9838 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8810    1.3598    0.1367 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9483    1.6728    1.2795 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3300    1.3316    1.1691 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7361    0.6614   -0.0904 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8526    1.6814   -1.1962 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1255   -1.2356    1.4361 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8799    0.4358    1.9820 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5080   -0.7970    2.0171 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8938    0.5534   -0.3708 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2883   -1.1427   -1.8398 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4018   -2.4747   -0.3810 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1320   -2.4093   -1.0929 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2547   -1.5689   -1.6211 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5784   -0.5254   -1.0683 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3525    0.1625   -2.2579 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8207   -1.9206    0.8767 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9237   -0.4561    1.9473 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3455   -0.9251    0.8997 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9388    1.4930    0.4532 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7205    1.9901   -0.7331 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3523    2.1616    2.1438 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0148    1.5453    1.9744 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5725    2.6832   -0.8016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9152    1.7705   -1.4966 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2353    1.4131   -2.0769 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  3  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  7 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 13  2  1  0
 13  6  1  0
  1 15  1  0
  1 16  1  0
  1 17  1  0
  2 18  1  0
  3 19  1  0
  4 20  1  0
  5 21  1  0
  8 22  1  0
  8 23  1  0
  8 24  1  0
  9 25  1  0
  9 26  1  0
  9 27  1  0
 10 28  1  0
 10 29  1  0
 11 30  1  0
 12 31  1  0
 14 32  1  0
 14 33  1  0
 14 34  1  0
M  END


  Mrv0541 05061309162D          

 14 15  0  0  0  0            999 V2000
    0.8838    0.0709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1681    2.9799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1075    2.9799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8371    0.2900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    2.1904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    0.8555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1712    1.5229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  1  0  0  0  0
  7  5  2  0  0  0  0
  9  1  1  0  0  0  0
 10  8  1  0  0  0  0
 10  9  1  0  0  0  0
 11  8  2  0  0  0  0
 12  2  1  0  0  0  0
 12  3  1  0  0  0  0
 12  6  1  0  0  0  0
 12 11  1  0  0  0  0
 13  4  1  0  0  0  0
 13  7  1  0  0  0  0
 13  9  1  0  0  0  0
 13 11  1  0  0  0  0
 14 10  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0036684

> <DATABASE_NAME>
hmdb

> <SMILES>
CC1C(O)C=C2C1(C)C=CCC2(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C13H20O/c1-9-10(14)8-11-12(2,3)6-5-7-13(9,11)4/h5,7-10,14H,6H2,1-4H3

> <INCHI_KEY>
MHUYBIUXLMLCJM-UHFFFAOYSA-N

> <FORMULA>
C13H20O

> <MOLECULAR_WEIGHT>
192.2973

> <EXACT_MASS>
192.151415262

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_AVERAGE_POLARIZABILITY>
22.83283641661321

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1,4,4,7a-tetramethyl-2,4,5,7a-tetrahydro-1H-inden-2-ol

> <ALOGPS_LOGP>
4.00

> <JCHEM_LOGP>
2.476066902666667

> <ALOGPS_LOGS>
-2.73

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.441599012649647

> <JCHEM_PKA_STRONGEST_BASIC>
-1.2934445918670434

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
60.9545

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.58e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1,4,4,7a-tetramethyl-2,5-dihydro-1H-inden-2-ol

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0036684
     RDKit          3D
2,4,5,7alpha-Tetrahydro-1,4,4,7a-tetramethyl-1H-inden-2-ol
 34 35  0  0  0  0  0  0  0  0999 V2000
   -2.3791   -0.4056    1.4709 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0598   -0.0497    0.0432 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8726   -1.2706   -0.8270 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4519   -2.3593   -0.1581 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4150   -1.4771   -0.8057 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2315   -0.4045   -0.3941 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6976   -0.1040   -0.1975 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5054   -0.4995   -1.4044 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2492   -0.8898    0.9838 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8810    1.3598    0.1367 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9483    1.6728    1.2795 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3300    1.3316    1.1691 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7361    0.6614   -0.0904 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8526    1.6814   -1.1962 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1255   -1.2356    1.4361 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8799    0.4358    1.9820 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5080   -0.7970    2.0171 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8938    0.5534   -0.3708 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2883   -1.1427   -1.8398 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4018   -2.4747   -0.3810 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1320   -2.4093   -1.0929 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2547   -1.5689   -1.6211 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5784   -0.5254   -1.0683 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3525    0.1625   -2.2579 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8207   -1.9206    0.8767 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9237   -0.4561    1.9473 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3455   -0.9251    0.8997 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9388    1.4930    0.4532 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7205    1.9901   -0.7331 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3523    2.1616    2.1438 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0148    1.5453    1.9744 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5725    2.6832   -0.8016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9152    1.7705   -1.4966 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2353    1.4131   -2.0769 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  3  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  7 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 13  2  1  0
 13  6  1  0
  1 15  1  0
  1 16  1  0
  1 17  1  0
  2 18  1  0
  3 19  1  0
  4 20  1  0
  5 21  1  0
  8 22  1  0
  8 23  1  0
  8 24  1  0
  9 25  1  0
  9 26  1  0
  9 27  1  0
 10 28  1  0
 10 29  1  0
 11 30  1  0
 12 31  1  0
 14 32  1  0
 14 33  1  0
 14 34  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       1.650   0.132   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.914   5.562   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.934   5.562   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.429   0.541   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.258   2.073   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.258   3.613   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.924   1.303   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.126   4.089   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.126   1.597   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.220   2.843   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.590   3.613   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.924   4.383   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.590   2.073   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -0.320   2.843   0.000  0.00  0.00           O+0
CONECT    1    9                                                            
CONECT    2   12                                                            
CONECT    3   12                                                            
CONECT    4   13                                                            
CONECT    5    6    7                                                       
CONECT    6    5   12                                                       
CONECT    7    5   13                                                       
CONECT    8   10   11                                                       
CONECT    9    1   10   13                                                  
CONECT   10    8    9   14                                                  
CONECT   11    8   12   13                                                  
CONECT   12    2    3    6   11                                             
CONECT   13    4    7    9   11                                             
CONECT   14   10                                                            
MASTER        0    0    0    0    0    0    0    0   14    0   30    0
END

COMPND    HMDB0036684
HETATM    1  C1  UNL     1      -2.379  -0.406   1.471  1.00  0.00           C  
HETATM    2  C2  UNL     1      -2.060  -0.050   0.043  1.00  0.00           C  
HETATM    3  C3  UNL     1      -1.873  -1.271  -0.827  1.00  0.00           C  
HETATM    4  O1  UNL     1      -2.452  -2.359  -0.158  1.00  0.00           O  
HETATM    5  C4  UNL     1      -0.415  -1.477  -0.806  1.00  0.00           C  
HETATM    6  C5  UNL     1       0.232  -0.405  -0.394  1.00  0.00           C  
HETATM    7  C6  UNL     1       1.698  -0.104  -0.197  1.00  0.00           C  
HETATM    8  C7  UNL     1       2.505  -0.500  -1.404  1.00  0.00           C  
HETATM    9  C8  UNL     1       2.249  -0.890   0.984  1.00  0.00           C  
HETATM   10  C9  UNL     1       1.881   1.360   0.137  1.00  0.00           C  
HETATM   11  C10 UNL     1       0.948   1.673   1.280  1.00  0.00           C  
HETATM   12  C11 UNL     1      -0.330   1.332   1.169  1.00  0.00           C  
HETATM   13  C12 UNL     1      -0.736   0.661  -0.090  1.00  0.00           C  
HETATM   14  C13 UNL     1      -0.853   1.681  -1.196  1.00  0.00           C  
HETATM   15  H1  UNL     1      -3.125  -1.236   1.436  1.00  0.00           H  
HETATM   16  H2  UNL     1      -2.880   0.436   1.982  1.00  0.00           H  
HETATM   17  H3  UNL     1      -1.508  -0.797   2.017  1.00  0.00           H  
HETATM   18  H4  UNL     1      -2.894   0.553  -0.371  1.00  0.00           H  
HETATM   19  H5  UNL     1      -2.288  -1.143  -1.840  1.00  0.00           H  
HETATM   20  H6  UNL     1      -3.402  -2.475  -0.381  1.00  0.00           H  
HETATM   21  H7  UNL     1       0.132  -2.409  -1.093  1.00  0.00           H  
HETATM   22  H8  UNL     1       2.255  -1.569  -1.621  1.00  0.00           H  
HETATM   23  H9  UNL     1       3.578  -0.525  -1.068  1.00  0.00           H  
HETATM   24  H10 UNL     1       2.352   0.162  -2.258  1.00  0.00           H  
HETATM   25  H11 UNL     1       1.821  -1.921   0.877  1.00  0.00           H  
HETATM   26  H12 UNL     1       1.924  -0.456   1.947  1.00  0.00           H  
HETATM   27  H13 UNL     1       3.345  -0.925   0.900  1.00  0.00           H  
HETATM   28  H14 UNL     1       2.939   1.493   0.453  1.00  0.00           H  
HETATM   29  H15 UNL     1       1.721   1.990  -0.733  1.00  0.00           H  
HETATM   30  H16 UNL     1       1.352   2.162   2.144  1.00  0.00           H  
HETATM   31  H17 UNL     1      -1.015   1.545   1.974  1.00  0.00           H  
HETATM   32  H18 UNL     1      -0.572   2.683  -0.802  1.00  0.00           H  
HETATM   33  H19 UNL     1      -1.915   1.771  -1.497  1.00  0.00           H  
HETATM   34  H20 UNL     1      -0.235   1.413  -2.077  1.00  0.00           H  
CONECT    1    2   15   16   17
CONECT    2    3   13   18
CONECT    3    4    5   19
CONECT    4   20
CONECT    5    6    6   21
CONECT    6    7   13
CONECT    7    8    9   10
CONECT    8   22   23   24
CONECT    9   25   26   27
CONECT   10   11   28   29
CONECT   11   12   12   30
CONECT   12   13   31
CONECT   13   14
CONECT   14   32   33   34
END

HMDB0036684
     RDKit          3D
2,4,5,7alpha-Tetrahydro-1,4,4,7a-tetramethyl-1H-inden-2-ol
 34 35  0  0  0  0  0  0  0  0999 V2000
   -2.3791   -0.4056    1.4709 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0598   -0.0497    0.0432 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8726   -1.2706   -0.8270 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4519   -2.3593   -0.1581 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4150   -1.4771   -0.8057 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2315   -0.4045   -0.3941 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6976   -0.1040   -0.1975 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5054   -0.4995   -1.4044 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2492   -0.8898    0.9838 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8810    1.3598    0.1367 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9483    1.6728    1.2795 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3300    1.3316    1.1691 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7361    0.6614   -0.0904 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8526    1.6814   -1.1962 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1255   -1.2356    1.4361 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8799    0.4358    1.9820 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5080   -0.7970    2.0171 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8938    0.5534   -0.3708 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2883   -1.1427   -1.8398 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4018   -2.4747   -0.3810 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1320   -2.4093   -1.0929 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2547   -1.5689   -1.6211 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5784   -0.5254   -1.0683 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3525    0.1625   -2.2579 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8207   -1.9206    0.8767 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9237   -0.4561    1.9473 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3455   -0.9251    0.8997 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9388    1.4930    0.4532 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7205    1.9901   -0.7331 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3523    2.1616    2.1438 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0148    1.5453    1.9744 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5725    2.6832   -0.8016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9152    1.7705   -1.4966 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2353    1.4131   -2.0769 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  3  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  7 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 13  2  1  0
 13  6  1  0
  1 15  1  0
  1 16  1  0
  1 17  1  0
  2 18  1  0
  3 19  1  0
  4 20  1  0
  5 21  1  0
  8 22  1  0
  8 23  1  0
  8 24  1  0
  9 25  1  0
  9 26  1  0
  9 27  1  0
 10 28  1  0
 10 29  1  0
 11 30  1  0
 12 31  1  0
 14 32  1  0
 14 33  1  0
 14 34  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
2,4,5,7a-Tetrahydro-1,4,4,7a-tetramethyl-1H-inden-2-ol	Generator
2,4,5,7Α-tetrahydro-1,4,4,7a-tetramethyl-1H-inden-2-ol	Generator
2,2,6,7-tetramethylbicyclo[4.3.0]Nona-1(9),4-dien-8-ol	HMDB

Chemical Formula

C₁₃H₂₀O

Average Molecular Weight

192.2973

Monoisotopic Molecular Weight

192.151415262

IUPAC Name

1,4,4,7a-tetramethyl-2,4,5,7a-tetrahydro-1H-inden-2-ol

Traditional Name

1,4,4,7a-tetramethyl-2,5-dihydro-1H-inden-2-ol

CAS Registry Number

99901-23-2

SMILES

CC1C(O)C=C2C1(C)C=CCC2(C)C

InChI Identifier

InChI=1S/C13H20O/c1-9-10(14)8-11-12(2,3)6-5-7-13(9,11)4/h5,7-10,14H,6H2,1-4H3

InChI Key

MHUYBIUXLMLCJM-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as secondary alcohols. Secondary alcohols are compounds containing a secondary alcohol functional group, with the general structure HOC(R)(R') (R,R'=alkyl, aryl).

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Alcohols and polyols

Direct Parent

Secondary alcohols

Alternative Parents

Hydrocarbon derivatives

Substituents

Secondary alcohol
Hydrocarbon derivative
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cell membrane (HMDB: HMDB0036684)

Cellular substructure

Extracellular (HMDB: HMDB0036684)
Membrane (HMDB: HMDB0036684)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0036684)

Source

Endogenous

Endogenous (HMDB: HMDB0036684)

Plant

Plant (HMDB: HMDB0036684)

Exogenous

Food

Food (HMDB: HMDB0036684)

Fruit

Pome

Quince (FooDB: FOOD00069)

Fruits (FooDB: FOOD00871)

Process

Naturally occurring process

Biological process

Cellular process

Cell signaling (HMDB: HMDB0036684)

Role

Biological role

Membrane stabilizer (HMDB: HMDB0036684)

Nutrient

Nutrient (HMDB: HMDB0036684)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0036684)

Emulsifier (HMDB: HMDB0036684)

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	4	ALOGPS
logP	2.48	ChemAxon
logS	-2.7	ALOGPS
pKa (Strongest Acidic)	18.44	ChemAxon
pKa (Strongest Basic)	-1.3	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	0	ChemAxon
Refractivity	60.95 m³·mol⁻¹	ChemAxon
Polarizability	22.83 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	144.595	31661259
DarkChem	[M-H]-	141.807	31661259
DeepCCS	[M+H]+	147.816	30932474
DeepCCS	[M-H]-	145.42	30932474
DeepCCS	[M-2H]-	179.465	30932474
DeepCCS	[M+Na]+	154.182	30932474
AllCCS	[M+H]+	142.2	32859911
AllCCS	[M+H-H2O]+	138.1	32859911
AllCCS	[M+NH4]+	146.1	32859911
AllCCS	[M+Na]+	147.2	32859911
AllCCS	[M-H]-	149.2	32859911
AllCCS	[M+Na-2H]-	149.9	32859911
AllCCS	[M+HCOO]-	150.7	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
2,4,5,7alpha-Tetrahydro-1,4,4,7a-tetramethyl-1H-inden-2-ol	CC1C(O)C=C2C1(C)C=CCC2(C)C	1967.1	Standard polar	33892256
2,4,5,7alpha-Tetrahydro-1,4,4,7a-tetramethyl-1H-inden-2-ol	CC1C(O)C=C2C1(C)C=CCC2(C)C	1339.9	Standard non polar	33892256
2,4,5,7alpha-Tetrahydro-1,4,4,7a-tetramethyl-1H-inden-2-ol	CC1C(O)C=C2C1(C)C=CCC2(C)C	1394.3	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
2,4,5,7alpha-Tetrahydro-1,4,4,7a-tetramethyl-1H-inden-2-ol,1TMS,isomer #1	CC1C(O[Si](C)(C)C)C=C2C(C)(C)CC=CC21C	1492.9	Semi standard non polar	33892256
2,4,5,7alpha-Tetrahydro-1,4,4,7a-tetramethyl-1H-inden-2-ol,1TBDMS,isomer #1	CC1C(O[Si](C)(C)C(C)(C)C)C=C2C(C)(C)CC=CC21C	1731.5	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 - 2,4,5,7alpha-Tetrahydro-1,4,4,7a-tetramethyl-1H-inden-2-ol GC-MS (Non-derivatized) - 70eV, Positive	splash10-00c0-1900000000-ebf0077016c667287f50	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2,4,5,7alpha-Tetrahydro-1,4,4,7a-tetramethyl-1H-inden-2-ol GC-MS (1 TMS) - 70eV, Positive	splash10-0072-5590000000-331e7be963660e39f017	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2,4,5,7alpha-Tetrahydro-1,4,4,7a-tetramethyl-1H-inden-2-ol 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 - 2,4,5,7alpha-Tetrahydro-1,4,4,7a-tetramethyl-1H-inden-2-ol 10V, Positive-QTOF	splash10-004l-0900000000-9399e32465726725d999	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,4,5,7alpha-Tetrahydro-1,4,4,7a-tetramethyl-1H-inden-2-ol 20V, Positive-QTOF	splash10-004l-2900000000-c0bbb3cdda76b22f3fa5	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,4,5,7alpha-Tetrahydro-1,4,4,7a-tetramethyl-1H-inden-2-ol 40V, Positive-QTOF	splash10-0zfs-9700000000-dd2a84b036bb7de7c7ee	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,4,5,7alpha-Tetrahydro-1,4,4,7a-tetramethyl-1H-inden-2-ol 10V, Negative-QTOF	splash10-0006-0900000000-97b73cb6168190ef66d8	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,4,5,7alpha-Tetrahydro-1,4,4,7a-tetramethyl-1H-inden-2-ol 20V, Negative-QTOF	splash10-0006-0900000000-2d8babdbbb99094b026c	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,4,5,7alpha-Tetrahydro-1,4,4,7a-tetramethyl-1H-inden-2-ol 40V, Negative-QTOF	splash10-057l-0900000000-b34cfdc31e025f9d322d	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,4,5,7alpha-Tetrahydro-1,4,4,7a-tetramethyl-1H-inden-2-ol 10V, Positive-QTOF	splash10-002f-0900000000-f5ecd597d9bc4f9a01fb	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,4,5,7alpha-Tetrahydro-1,4,4,7a-tetramethyl-1H-inden-2-ol 20V, Positive-QTOF	splash10-002f-5900000000-6b765b0a64e161fe0957	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,4,5,7alpha-Tetrahydro-1,4,4,7a-tetramethyl-1H-inden-2-ol 40V, Positive-QTOF	splash10-00n3-9400000000-dffb52b7be5b1aa1f64f	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,4,5,7alpha-Tetrahydro-1,4,4,7a-tetramethyl-1H-inden-2-ol 10V, Negative-QTOF	splash10-0006-0900000000-14436e4d9ff8d032db54	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,4,5,7alpha-Tetrahydro-1,4,4,7a-tetramethyl-1H-inden-2-ol 20V, Negative-QTOF	splash10-0006-0900000000-14436e4d9ff8d032db54	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,4,5,7alpha-Tetrahydro-1,4,4,7a-tetramethyl-1H-inden-2-ol 40V, Negative-QTOF	splash10-0006-0900000000-04cd65950c9e0af402f8	2021-09-22	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

FDB015614

KNApSAcK ID

C00021957

Chemspider ID

35014199

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

66963592

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 2,4,5,7alpha-Tetrahydro-1,4,4,7a-tetramethyl-1H-inden-2-ol (HMDB0036684)

MOL for HMDB0036684 (2,4,5,7alpha-Tetrahydro-1,4,4,7a-tetramethyl-1H-inden-2-ol)

3D MOL for HMDB0036684 (2,4,5,7alpha-Tetrahydro-1,4,4,7a-tetramethyl-1H-inden-2-ol)

3D SDF for HMDB0036684 (2,4,5,7alpha-Tetrahydro-1,4,4,7a-tetramethyl-1H-inden-2-ol)

3D-SDF for HMDB0036684 (2,4,5,7alpha-Tetrahydro-1,4,4,7a-tetramethyl-1H-inden-2-ol)

PDB for HMDB0036684 (2,4,5,7alpha-Tetrahydro-1,4,4,7a-tetramethyl-1H-inden-2-ol)

3D PDB for HMDB0036684 (2,4,5,7alpha-Tetrahydro-1,4,4,7a-tetramethyl-1H-inden-2-ol)

SMILES for HMDB0036684 (2,4,5,7alpha-Tetrahydro-1,4,4,7a-tetramethyl-1H-inden-2-ol)

INCHI for HMDB0036684 (2,4,5,7alpha-Tetrahydro-1,4,4,7a-tetramethyl-1H-inden-2-ol)

Structure for HMDB0036684 (2,4,5,7alpha-Tetrahydro-1,4,4,7a-tetramethyl-1H-inden-2-ol)

3D Structure for HMDB0036684 (2,4,5,7alpha-Tetrahydro-1,4,4,7a-tetramethyl-1H-inden-2-ol)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra