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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-12 01:31:46 UTC

Update Date

2022-03-07 02:56:25 UTC

HMDB ID

HMDB0039974

Secondary Accession Numbers

HMDB39974

Metabolite Identification

Common Name

(1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol

Description

(1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol belongs to the class of organic compounds known as menthane monoterpenoids. These are monoterpenoids with a structure based on the o-, m-, or p-menthane backbone. P-menthane consists of the cyclohexane ring with a methyl group and a (2-methyl)-propyl group at the 1 and 4 ring position, respectively. The o- and m- menthanes are much rarer, and presumably arise by alkyl migration of p-menthanes. Based on a literature review a small amount of articles have been published on (1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol.

Structure

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

HMDB0039974
     RDKit          3D
(1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol
 34 34  0  0  0  0  0  0  0  0999 V2000
    2.5502   -0.8911   -0.9585 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3718    0.0425    0.2246 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6088    0.3934    0.7226 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6057   -0.6443    1.3274 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2075   -0.9915    0.9412 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5688    0.1239    0.3285 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7946   -0.4485   -0.3288 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6435   -1.1574    0.7100 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4487   -1.3986   -1.2892 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6456    0.5878   -1.0071 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0592    1.5983   -0.1523 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2068    0.9923   -0.6025 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6041    1.2703   -0.1727 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6784    2.1775    0.8894 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6258   -1.5006   -1.1211 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4269   -1.5158   -0.7623 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7204   -0.2454   -1.8478 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9553    1.2442    0.3917 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5757    0.0385    2.1938 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1334   -1.6078    1.5622 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3299   -1.2805    1.8919 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1629   -1.9258    0.3092 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9231    0.7807    1.1738 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5788   -1.5391    0.2804 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8391   -0.4028    1.5154 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0962   -2.0136    1.1729 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5488   -2.3143   -0.9577 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1581    0.9851   -1.9359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5648    0.0721   -1.3599 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1784    2.4123   -0.7266 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2281    0.6213   -1.6463 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3288    1.9819   -0.6531 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1282    1.7668   -1.0315 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9164    2.7883    0.9182 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  7 10  1  0
 10 11  1  0
  6 12  1  0
 12 13  1  0
 13 14  1  0
 13  2  1  0
  1 15  1  0
  1 16  1  0
  1 17  1  0
  3 18  1  0
  4 19  1  0
  4 20  1  0
  5 21  1  0
  5 22  1  0
  6 23  1  0
  8 24  1  0
  8 25  1  0
  8 26  1  0
  9 27  1  0
 10 28  1  0
 10 29  1  0
 11 30  1  0
 12 31  1  0
 12 32  1  0
 13 33  1  0
 14 34  1  0
M  END

  Mrv0541 02241207492D          

 14 14  0  0  0  0            999 V2000
   -1.0710    0.9542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0710    0.1292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3575   -0.2832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3546    0.1292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3546    0.9542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3575    1.3653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0492    1.8150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2405    1.9333    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0697    1.3667    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3575   -1.1083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0725   -1.5208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3574   -1.5208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3575   -1.9333    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0725   -1.1083    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  6  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3 10  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  9  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 10 13  1  0  0  0  0
 12 14  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0039974

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(O)(CO)C1CCC(C)(O)C(O)C1

> <INCHI_IDENTIFIER>
InChI=1S/C10H20O4/c1-9(13)4-3-7(5-8(9)12)10(2,14)6-11/h7-8,11-14H,3-6H2,1-2H3

> <INCHI_KEY>
QEFNQQRVZDFDIJ-UHFFFAOYSA-N

> <FORMULA>
C10H20O4

> <MOLECULAR_WEIGHT>
204.2634

> <EXACT_MASS>
204.136159128

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_AVERAGE_POLARIZABILITY>
22.138140333828293

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4-(1,2-dihydroxypropan-2-yl)-1-methylcyclohexane-1,2-diol

> <ALOGPS_LOGP>
-0.48

> <JCHEM_LOGP>
-0.9350975396666668

> <ALOGPS_LOGS>
-0.26

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.076828736135628

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.49315569244352

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0715866598061323

> <JCHEM_POLAR_SURFACE_AREA>
80.92

> <JCHEM_REFRACTIVITY>
52.276199999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.12e+02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-(1,2-dihydroxypropan-2-yl)-1-methylcyclohexane-1,2-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0039974
     RDKit          3D
(1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol
 34 34  0  0  0  0  0  0  0  0999 V2000
    2.5502   -0.8911   -0.9585 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3718    0.0425    0.2246 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6088    0.3934    0.7226 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6057   -0.6443    1.3274 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2075   -0.9915    0.9412 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5688    0.1239    0.3285 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7946   -0.4485   -0.3288 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6435   -1.1574    0.7100 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4487   -1.3986   -1.2892 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6456    0.5878   -1.0071 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0592    1.5983   -0.1523 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2068    0.9923   -0.6025 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6041    1.2703   -0.1727 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6784    2.1775    0.8894 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6258   -1.5006   -1.1211 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4269   -1.5158   -0.7623 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7204   -0.2454   -1.8478 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9553    1.2442    0.3917 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5757    0.0385    2.1938 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1334   -1.6078    1.5622 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3299   -1.2805    1.8919 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1629   -1.9258    0.3092 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9231    0.7807    1.1738 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5788   -1.5391    0.2804 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8391   -0.4028    1.5154 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0962   -2.0136    1.1729 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5488   -2.3143   -0.9577 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1581    0.9851   -1.9359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5648    0.0721   -1.3599 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1784    2.4123   -0.7266 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2281    0.6213   -1.6463 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3288    1.9819   -0.6531 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1282    1.7668   -1.0315 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9164    2.7883    0.9182 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  7 10  1  0
 10 11  1  0
  6 12  1  0
 12 13  1  0
 13 14  1  0
 13  2  1  0
  1 15  1  0
  1 16  1  0
  1 17  1  0
  3 18  1  0
  4 19  1  0
  4 20  1  0
  5 21  1  0
  5 22  1  0
  6 23  1  0
  8 24  1  0
  8 25  1  0
  8 26  1  0
  9 27  1  0
 10 28  1  0
 10 29  1  0
 11 30  1  0
 12 31  1  0
 12 32  1  0
 13 33  1  0
 14 34  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      -1.999   1.781   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.999   0.241   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.667  -0.529   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.662   0.241   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.662   1.781   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.667   2.549   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.959   3.388   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       0.449   3.609   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0       1.997   2.551   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -0.667  -2.069   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.002  -2.839   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.667  -2.839   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -0.667  -3.609   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0       2.002  -2.069   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4   10                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    9                                                  
CONECT    6    1    5    7    8                                             
CONECT    7    6                                                            
CONECT    8    6                                                            
CONECT    9    5                                                            
CONECT   10    3   11   12   13                                             
CONECT   11   10                                                            
CONECT   12   10   14                                                       
CONECT   13   10                                                            
CONECT   14   12                                                            
MASTER        0    0    0    0    0    0    0    0   14    0   28    0
END

COMPND    HMDB0039974
HETATM    1  C1  UNL     1       2.550  -0.891  -0.958  1.00  0.00           C  
HETATM    2  C2  UNL     1       2.372   0.043   0.225  1.00  0.00           C  
HETATM    3  O1  UNL     1       3.609   0.393   0.723  1.00  0.00           O  
HETATM    4  C3  UNL     1       1.606  -0.644   1.327  1.00  0.00           C  
HETATM    5  C4  UNL     1       0.207  -0.991   0.941  1.00  0.00           C  
HETATM    6  C5  UNL     1      -0.569   0.124   0.328  1.00  0.00           C  
HETATM    7  C6  UNL     1      -1.795  -0.449  -0.329  1.00  0.00           C  
HETATM    8  C7  UNL     1      -2.643  -1.157   0.710  1.00  0.00           C  
HETATM    9  O2  UNL     1      -1.449  -1.399  -1.289  1.00  0.00           O  
HETATM   10  C8  UNL     1      -2.646   0.588  -1.007  1.00  0.00           C  
HETATM   11  O3  UNL     1      -3.059   1.598  -0.152  1.00  0.00           O  
HETATM   12  C9  UNL     1       0.207   0.992  -0.603  1.00  0.00           C  
HETATM   13  C10 UNL     1       1.604   1.270  -0.173  1.00  0.00           C  
HETATM   14  O4  UNL     1       1.678   2.178   0.889  1.00  0.00           O  
HETATM   15  H1  UNL     1       1.626  -1.501  -1.121  1.00  0.00           H  
HETATM   16  H2  UNL     1       3.427  -1.516  -0.762  1.00  0.00           H  
HETATM   17  H3  UNL     1       2.720  -0.245  -1.848  1.00  0.00           H  
HETATM   18  H4  UNL     1       3.955   1.244   0.392  1.00  0.00           H  
HETATM   19  H5  UNL     1       1.576   0.039   2.194  1.00  0.00           H  
HETATM   20  H6  UNL     1       2.133  -1.608   1.562  1.00  0.00           H  
HETATM   21  H7  UNL     1      -0.330  -1.281   1.892  1.00  0.00           H  
HETATM   22  H8  UNL     1       0.163  -1.926   0.309  1.00  0.00           H  
HETATM   23  H9  UNL     1      -0.923   0.781   1.174  1.00  0.00           H  
HETATM   24  H10 UNL     1      -3.579  -1.539   0.280  1.00  0.00           H  
HETATM   25  H11 UNL     1      -2.839  -0.403   1.515  1.00  0.00           H  
HETATM   26  H12 UNL     1      -2.096  -2.014   1.173  1.00  0.00           H  
HETATM   27  H13 UNL     1      -1.549  -2.314  -0.958  1.00  0.00           H  
HETATM   28  H14 UNL     1      -2.158   0.985  -1.936  1.00  0.00           H  
HETATM   29  H15 UNL     1      -3.565   0.072  -1.360  1.00  0.00           H  
HETATM   30  H16 UNL     1      -3.178   2.412  -0.727  1.00  0.00           H  
HETATM   31  H17 UNL     1       0.228   0.621  -1.646  1.00  0.00           H  
HETATM   32  H18 UNL     1      -0.329   1.982  -0.653  1.00  0.00           H  
HETATM   33  H19 UNL     1       2.128   1.767  -1.031  1.00  0.00           H  
HETATM   34  H20 UNL     1       0.916   2.788   0.918  1.00  0.00           H  
CONECT    1    2   15   16   17
CONECT    2    3    4   13
CONECT    3   18
CONECT    4    5   19   20
CONECT    5    6   21   22
CONECT    6    7   12   23
CONECT    7    8    9   10
CONECT    8   24   25   26
CONECT    9   27
CONECT   10   11   28   29
CONECT   11   30
CONECT   12   13   31   32
CONECT   13   14   33
CONECT   14   34
END

HMDB0039974
     RDKit          3D
(1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol
 34 34  0  0  0  0  0  0  0  0999 V2000
    2.5502   -0.8911   -0.9585 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3718    0.0425    0.2246 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6088    0.3934    0.7226 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6057   -0.6443    1.3274 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2075   -0.9915    0.9412 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5688    0.1239    0.3285 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7946   -0.4485   -0.3288 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6435   -1.1574    0.7100 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4487   -1.3986   -1.2892 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6456    0.5878   -1.0071 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0592    1.5983   -0.1523 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2068    0.9923   -0.6025 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6041    1.2703   -0.1727 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6784    2.1775    0.8894 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6258   -1.5006   -1.1211 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4269   -1.5158   -0.7623 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7204   -0.2454   -1.8478 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9553    1.2442    0.3917 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5757    0.0385    2.1938 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1334   -1.6078    1.5622 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3299   -1.2805    1.8919 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1629   -1.9258    0.3092 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9231    0.7807    1.1738 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5788   -1.5391    0.2804 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8391   -0.4028    1.5154 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0962   -2.0136    1.1729 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5488   -2.3143   -0.9577 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1581    0.9851   -1.9359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5648    0.0721   -1.3599 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1784    2.4123   -0.7266 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2281    0.6213   -1.6463 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3288    1.9819   -0.6531 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1282    1.7668   -1.0315 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9164    2.7883    0.9182 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  7 10  1  0
 10 11  1  0
  6 12  1  0
 12 13  1  0
 13 14  1  0
 13  2  1  0
  1 15  1  0
  1 16  1  0
  1 17  1  0
  3 18  1  0
  4 19  1  0
  4 20  1  0
  5 21  1  0
  5 22  1  0
  6 23  1  0
  8 24  1  0
  8 25  1  0
  8 26  1  0
  9 27  1  0
 10 28  1  0
 10 29  1  0
 11 30  1  0
 12 31  1  0
 12 32  1  0
 13 33  1  0
 14 34  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₁₀H₂₀O₄

Average Molecular Weight

204.2634

Monoisotopic Molecular Weight

204.136159128

IUPAC Name

4-(1,2-dihydroxypropan-2-yl)-1-methylcyclohexane-1,2-diol

Traditional Name

4-(1,2-dihydroxypropan-2-yl)-1-methylcyclohexane-1,2-diol

CAS Registry Number

402593-46-8

SMILES

CC(O)(CO)C1CCC(C)(O)C(O)C1

InChI Identifier

InChI=1S/C10H20O4/c1-9(13)4-3-7(5-8(9)12)10(2,14)6-11/h7-8,11-14H,3-6H2,1-2H3

InChI Key

QEFNQQRVZDFDIJ-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as menthane monoterpenoids. These are monoterpenoids with a structure based on the o-, m-, or p-menthane backbone. P-menthane consists of the cyclohexane ring with a methyl group and a (2-methyl)-propyl group at the 1 and 4 ring position, respectively. The o- and m- menthanes are much rarer, and presumably arise by alkyl migration of p-menthanes.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Monoterpenoids

Direct Parent

Menthane monoterpenoids

Alternative Parents

Substituents

P-menthane monoterpenoid
Monocyclic monoterpenoid
Cyclohexanol
Tertiary alcohol
Cyclic alcohol
Secondary alcohol
Organic oxygen compound
Hydrocarbon derivative
Primary alcohol
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: HMDB0039974)

Source

Exogenous

Food

Food (HMDB: HMDB0039974)

Herb and spice

Herbs and Spices (FooDB: FOOD00866)

Fat and oil

Fats and oils (FooDB: FOOD00864)

Exogenous (HMDB: HMDB0039974)

Endogenous

Plant

Plant (HMDB: HMDB0039974)

Animal

Animal (HMDB: HMDB0039974)

Endogenous (HMDB: HMDB0039974)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid Peroxidation (HMDB: HMDB0039974)

Biochemical pathway

Metabolic pathway

Fatty Acid Metabolism (HMDB: HMDB0039974)

Lipid metabolism pathway (HMDB: HMDB0039974)

Cellular process

Cell signaling (HMDB: HMDB0039974)

Biochemical process

Lipid transport (HMDB: HMDB0039974)

Role

Biological role

Energy source (HMDB: HMDB0039974)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0039974)

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	112 g/L	ALOGPS
logP	-0.48	ALOGPS
logP	-0.94	ChemAxon
logS	-0.26	ALOGPS
pKa (Strongest Acidic)	13.49	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	80.92 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	52.28 m³·mol⁻¹	ChemAxon
Polarizability	22.14 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	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]+	147.383	31661259
DarkChem	[M-H]-	142.67	31661259
DeepCCS	[M+H]+	145.757	30932474
DeepCCS	[M-H]-	143.399	30932474
DeepCCS	[M-2H]-	178.458	30932474
DeepCCS	[M+Na]+	153.678	30932474
AllCCS	[M+H]+	147.3	32859911
AllCCS	[M+H-H2O]+	143.3	32859911
AllCCS	[M+NH4]+	150.9	32859911
AllCCS	[M+Na]+	151.9	32859911
AllCCS	[M-H]-	148.3	32859911
AllCCS	[M+Na-2H]-	149.3	32859911
AllCCS	[M+HCOO]-	150.5	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
(1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol	CC(O)(CO)C1CCC(C)(O)C(O)C1	3278.7	Standard polar	33892256
(1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol	CC(O)(CO)C1CCC(C)(O)C(O)C1	1712.6	Standard non polar	33892256
(1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol	CC(O)(CO)C1CCC(C)(O)C(O)C1	1747.0	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
(1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol,1TMS,isomer #1	CC1(O)CCC(C(C)(CO)O[Si](C)(C)C)CC1O	1890.7	Semi standard non polar	33892256
(1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol,1TMS,isomer #2	CC1(O)CCC(C(C)(O)CO[Si](C)(C)C)CC1O	1882.3	Semi standard non polar	33892256
(1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol,1TMS,isomer #3	CC(O)(CO)C1CCC(C)(O[Si](C)(C)C)C(O)C1	1882.0	Semi standard non polar	33892256
(1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol,1TMS,isomer #4	CC(O)(CO)C1CCC(C)(O)C(O[Si](C)(C)C)C1	1860.5	Semi standard non polar	33892256
(1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol,2TMS,isomer #1	CC1(O[Si](C)(C)C)CCC(C(C)(CO)O[Si](C)(C)C)CC1O	1887.2	Semi standard non polar	33892256
(1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol,2TMS,isomer #2	CC1(O)CCC(C(C)(CO[Si](C)(C)C)O[Si](C)(C)C)CC1O	1916.7	Semi standard non polar	33892256
(1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol,2TMS,isomer #3	CC1(O)CCC(C(C)(CO)O[Si](C)(C)C)CC1O[Si](C)(C)C	1868.9	Semi standard non polar	33892256
(1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol,2TMS,isomer #4	CC(O)(CO[Si](C)(C)C)C1CCC(C)(O[Si](C)(C)C)C(O)C1	1881.0	Semi standard non polar	33892256
(1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol,2TMS,isomer #5	CC(O)(CO[Si](C)(C)C)C1CCC(C)(O)C(O[Si](C)(C)C)C1	1871.0	Semi standard non polar	33892256
(1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol,2TMS,isomer #6	CC(O)(CO)C1CCC(C)(O[Si](C)(C)C)C(O[Si](C)(C)C)C1	1883.4	Semi standard non polar	33892256
(1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol,3TMS,isomer #1	CC1(O[Si](C)(C)C)CCC(C(C)(CO[Si](C)(C)C)O[Si](C)(C)C)CC1O	1907.7	Semi standard non polar	33892256
(1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol,3TMS,isomer #2	CC(CO)(O[Si](C)(C)C)C1CCC(C)(O[Si](C)(C)C)C(O[Si](C)(C)C)C1	1890.1	Semi standard non polar	33892256
(1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol,3TMS,isomer #3	CC1(O)CCC(C(C)(CO[Si](C)(C)C)O[Si](C)(C)C)CC1O[Si](C)(C)C	1875.2	Semi standard non polar	33892256
(1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol,3TMS,isomer #4	CC(O)(CO[Si](C)(C)C)C1CCC(C)(O[Si](C)(C)C)C(O[Si](C)(C)C)C1	1872.6	Semi standard non polar	33892256
(1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol,4TMS,isomer #1	CC(CO[Si](C)(C)C)(O[Si](C)(C)C)C1CCC(C)(O[Si](C)(C)C)C(O[Si](C)(C)C)C1	1926.9	Semi standard non polar	33892256
(1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol,1TBDMS,isomer #1	CC1(O)CCC(C(C)(CO)O[Si](C)(C)C(C)(C)C)CC1O	2138.1	Semi standard non polar	33892256
(1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol,1TBDMS,isomer #2	CC1(O)CCC(C(C)(O)CO[Si](C)(C)C(C)(C)C)CC1O	2115.3	Semi standard non polar	33892256
(1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol,1TBDMS,isomer #3	CC(O)(CO)C1CCC(C)(O[Si](C)(C)C(C)(C)C)C(O)C1	2116.5	Semi standard non polar	33892256
(1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol,1TBDMS,isomer #4	CC(O)(CO)C1CCC(C)(O)C(O[Si](C)(C)C(C)(C)C)C1	2096.3	Semi standard non polar	33892256
(1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol,2TBDMS,isomer #1	CC1(O[Si](C)(C)C(C)(C)C)CCC(C(C)(CO)O[Si](C)(C)C(C)(C)C)CC1O	2324.6	Semi standard non polar	33892256
(1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol,2TBDMS,isomer #2	CC1(O)CCC(C(C)(CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)CC1O	2380.9	Semi standard non polar	33892256
(1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol,2TBDMS,isomer #3	CC1(O)CCC(C(C)(CO)O[Si](C)(C)C(C)(C)C)CC1O[Si](C)(C)C(C)(C)C	2300.8	Semi standard non polar	33892256
(1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol,2TBDMS,isomer #4	CC(O)(CO[Si](C)(C)C(C)(C)C)C1CCC(C)(O[Si](C)(C)C(C)(C)C)C(O)C1	2308.5	Semi standard non polar	33892256
(1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol,2TBDMS,isomer #5	CC(O)(CO[Si](C)(C)C(C)(C)C)C1CCC(C)(O)C(O[Si](C)(C)C(C)(C)C)C1	2294.9	Semi standard non polar	33892256
(1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol,2TBDMS,isomer #6	CC(O)(CO)C1CCC(C)(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1	2345.9	Semi standard non polar	33892256
(1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol,3TBDMS,isomer #1	CC1(O[Si](C)(C)C(C)(C)C)CCC(C(C)(CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)CC1O	2547.1	Semi standard non polar	33892256
(1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol,3TBDMS,isomer #2	CC(CO)(O[Si](C)(C)C(C)(C)C)C1CCC(C)(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1	2545.8	Semi standard non polar	33892256
(1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol,3TBDMS,isomer #3	CC1(O)CCC(C(C)(CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)CC1O[Si](C)(C)C(C)(C)C	2530.8	Semi standard non polar	33892256
(1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol,3TBDMS,isomer #4	CC(O)(CO[Si](C)(C)C(C)(C)C)C1CCC(C)(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1	2531.8	Semi standard non polar	33892256
(1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol,4TBDMS,isomer #1	CC(CO[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)C1CCC(C)(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1	2795.5	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 - (1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol GC-MS (Non-derivatized) - 70eV, Positive	splash10-0079-7900000000-1f24c42cb49484437eb5	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol GC-MS (4 TMS) - 70eV, Positive	splash10-004i-6222900000-c60e94318c62dfb7da22	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol 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 - (1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol 10V, Positive-QTOF	splash10-0a4r-0980000000-f088f2e2357b48ff231d	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol 20V, Positive-QTOF	splash10-07br-0910000000-9be830ca2867b11210cd	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol 40V, Positive-QTOF	splash10-0cdi-9600000000-689bba521afc4b409d59	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol 10V, Negative-QTOF	splash10-0udi-0490000000-42a37d3ade952bb1e551	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol 20V, Negative-QTOF	splash10-0zp0-0920000000-9be9c9c1882ec6ca94ad	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol 40V, Negative-QTOF	splash10-0c29-3900000000-040f8491edcdf8eb2e8b	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol 10V, Negative-QTOF	splash10-0udi-0190000000-e911bbd7412aaf67f759	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol 20V, Negative-QTOF	splash10-0udi-0950000000-664e93dd4ce59354e887	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol 40V, Negative-QTOF	splash10-0a4i-3900000000-24d2142679f2a88e7184	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol 10V, Positive-QTOF	splash10-0ap0-0930000000-40184208337b7cdb880e	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol 20V, Positive-QTOF	splash10-0aor-7910000000-4d83560df2b13c891b05	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol 40V, Positive-QTOF	splash10-0abd-9100000000-d6cc64c262c4c734d830	2021-09-23	Wishart Lab	View Spectrum

NMR Spectra

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

Biological Properties

Cellular Locations

Cytoplasm
Extracellular
Membrane

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB019648

KNApSAcK ID

Not Available

Chemspider ID

99340

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

110677

PDB ID

Not Available

ChEBI ID

169020

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

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 (1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol (HMDB0039974)

MOL for HMDB0039974 ((1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol)

3D MOL for HMDB0039974 ((1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol)

3D SDF for HMDB0039974 ((1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol)

3D-SDF for HMDB0039974 ((1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol)

PDB for HMDB0039974 ((1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol)

3D PDB for HMDB0039974 ((1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol)

SMILES for HMDB0039974 ((1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol)

INCHI for HMDB0039974 ((1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol)

Structure for HMDB0039974 ((1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol)

3D Structure for HMDB0039974 ((1S,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra