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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 23:29:34 UTC

Update Date

2022-03-07 02:55:40 UTC

HMDB ID

HMDB0038213

Secondary Accession Numbers

HMDB38213

Metabolite Identification

Common Name

Humulol

Description

Humulol belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. Based on a literature review a small amount of articles have been published on Humulol.

Structure

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

HMDB0038213
     RDKit          3D
Humulol
 42 42  0  0  0  0  0  0  0  0999 V2000
   -0.2144    3.4930   -0.3115 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3612    2.2336    0.5297 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4379    1.5053    0.4263 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8182    0.2618    1.1166 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9352   -0.9530    0.2151 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1388   -0.6004   -1.2285 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2763   -1.6129    0.6401 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8879   -1.9723    0.4710 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2137   -2.2770   -0.1130 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9061   -1.7327   -1.2963 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0159   -0.7187   -0.8986 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1252   -1.4446   -0.1722 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4232   -0.1297   -2.0768 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3152    0.2280   -0.0069 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0052    1.3884    0.6014 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8299    2.0204    1.3984 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1129    3.6738   -0.9013 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    3.3967   -0.9353 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0124    4.3173    0.4056 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2233    1.8394   -0.2869 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7828    0.4825    1.6639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1196   -0.0118    1.9547 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5599    0.2283   -1.6155 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2266   -0.2942   -1.3749 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0455   -1.4852   -1.8880 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6550   -2.2545   -0.1567 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9781   -0.8168    0.9399 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0281   -2.1769    1.5767 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1428   -2.5819    1.3826 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7973   -3.1276    0.3439 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4668   -2.5062   -1.8592 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2948   -1.2013   -2.0185 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0850   -1.2039    0.9195 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9583   -2.5560   -0.2335 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1206   -1.1657   -0.6112 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4202   -0.0816   -2.0817 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5395    0.6884   -0.6482 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9554   -0.3858    0.8383 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7638    1.1514    1.3447 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2924    2.1742   -0.1237 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5454    1.2811    2.1703 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1681    2.9267    1.8993 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
  5  7  1  0
  5  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 11 13  1  0
 11 14  1  0
 14 15  1  0
 15 16  1  0
 16  2  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  3 20  1  0
  4 21  1  0
  4 22  1  0
  6 23  1  0
  6 24  1  0
  6 25  1  0
  7 26  1  0
  7 27  1  0
  7 28  1  0
  8 29  1  0
  9 30  1  0
 10 31  1  0
 10 32  1  0
 12 33  1  0
 12 34  1  0
 12 35  1  0
 13 36  1  0
 14 37  1  0
 14 38  1  0
 15 39  1  0
 15 40  1  0
 16 41  1  0
 16 42  1  0
M  END

  Mrv0541 02241219012D          

 16 16  0  0  0  0            999 V2000
   -3.6830   -4.3902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3975   -4.8027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3975   -5.6277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9686   -4.8027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2541   -4.3902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2541   -6.0402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5396   -5.6277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5396   -4.8027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6830   -6.0402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3340   -6.8248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5090   -6.8248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0241   -7.4922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8836   -7.5599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1120   -6.0402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2541   -3.5652    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9686   -3.9777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  9  2  0  0  0  0
  1  4  1  0  0  0  0
  5  4  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  5  8  1  0  0  0  0
 11  6  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
  3 14  1  0  0  0  0
  5 15  1  0  0  0  0
  5 16  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0038213

> <DATABASE_NAME>
hmdb

> <SMILES>
C\C1=C/CC(C)(C)\C=C\CC(C)(O)CCC1

> <INCHI_IDENTIFIER>
InChI=1S/C15H26O/c1-13-7-5-10-15(4,16)11-6-9-14(2,3)12-8-13/h6,8-9,16H,5,7,10-12H2,1-4H3/b9-6+,13-8+

> <INCHI_KEY>
ZLMAVMBYWKVCLV-IMWXLZLDSA-N

> <FORMULA>
C15H26O

> <MOLECULAR_WEIGHT>
222.3663

> <EXACT_MASS>
222.198365454

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_AVERAGE_POLARIZABILITY>
27.58273383669705

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3E,7E)-1,5,5,8-tetramethylcycloundeca-3,7-dien-1-ol

> <ALOGPS_LOGP>
5.04

> <JCHEM_LOGP>
3.8906976309999997

> <ALOGPS_LOGS>
-3.81

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
19.29646369594343

> <JCHEM_PKA_STRONGEST_BASIC>
-0.9195267793943439

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
72.45760000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.48e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3E,7E)-1,5,5,8-tetramethylcycloundeca-3,7-dien-1-ol

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0038213
     RDKit          3D
Humulol
 42 42  0  0  0  0  0  0  0  0999 V2000
   -0.2144    3.4930   -0.3115 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3612    2.2336    0.5297 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4379    1.5053    0.4263 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8182    0.2618    1.1166 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9352   -0.9530    0.2151 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1388   -0.6004   -1.2285 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2763   -1.6129    0.6401 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8879   -1.9723    0.4710 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2137   -2.2770   -0.1130 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9061   -1.7327   -1.2963 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0159   -0.7187   -0.8986 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1252   -1.4446   -0.1722 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4232   -0.1297   -2.0768 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3152    0.2280   -0.0069 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0052    1.3884    0.6014 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8299    2.0204    1.3984 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1129    3.6738   -0.9013 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    3.3967   -0.9353 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0124    4.3173    0.4056 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2233    1.8394   -0.2869 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7828    0.4825    1.6639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1196   -0.0118    1.9547 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5599    0.2283   -1.6155 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2266   -0.2942   -1.3749 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0455   -1.4852   -1.8880 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6550   -2.2545   -0.1567 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9781   -0.8168    0.9399 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0281   -2.1769    1.5767 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1428   -2.5819    1.3826 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7973   -3.1276    0.3439 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4668   -2.5062   -1.8592 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2948   -1.2013   -2.0185 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0850   -1.2039    0.9195 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9583   -2.5560   -0.2335 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1206   -1.1657   -0.6112 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4202   -0.0816   -2.0817 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5395    0.6884   -0.6482 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9554   -0.3858    0.8383 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7638    1.1514    1.3447 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2924    2.1742   -0.1237 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5454    1.2811    2.1703 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1681    2.9267    1.8993 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
  5  7  1  0
  5  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 11 13  1  0
 11 14  1  0
 14 15  1  0
 15 16  1  0
 16  2  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  3 20  1  0
  4 21  1  0
  4 22  1  0
  6 23  1  0
  6 24  1  0
  6 25  1  0
  7 26  1  0
  7 27  1  0
  7 28  1  0
  8 29  1  0
  9 30  1  0
 10 31  1  0
 10 32  1  0
 12 33  1  0
 12 34  1  0
 12 35  1  0
 13 36  1  0
 14 37  1  0
 14 38  1  0
 15 39  1  0
 15 40  1  0
 16 41  1  0
 16 42  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      -6.875  -8.195   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -8.209  -8.965   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -8.209 -10.505   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -5.541  -8.965   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -4.208  -8.195   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -4.208 -11.275   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.874 -10.505   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.874  -8.965   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -6.875 -11.275   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -6.223 -12.740   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -4.683 -12.740   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -3.778 -13.985   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -5.383 -14.112   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -9.542 -11.275   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -4.208  -6.655   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -5.541  -7.425   0.000  0.00  0.00           C+0
CONECT    1    2    4                                                       
CONECT    2    1    3                                                       
CONECT    3    2    9   14                                                  
CONECT    4    1    5                                                       
CONECT    5    4    8   15   16                                             
CONECT    6    7   11                                                       
CONECT    7    6    8                                                       
CONECT    8    7    5                                                       
CONECT    9    3   10                                                       
CONECT   10    9   11                                                       
CONECT   11    6   10   12   13                                             
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14    3                                                            
CONECT   15    5                                                            
CONECT   16    5                                                            
MASTER        0    0    0    0    0    0    0    0   16    0   32    0
END

COMPND    HMDB0038213
HETATM    1  C1  UNL     1      -0.214   3.493  -0.311  1.00  0.00           C  
HETATM    2  C2  UNL     1      -0.361   2.234   0.530  1.00  0.00           C  
HETATM    3  C3  UNL     1      -1.438   1.505   0.426  1.00  0.00           C  
HETATM    4  C4  UNL     1      -1.818   0.262   1.117  1.00  0.00           C  
HETATM    5  C5  UNL     1      -1.935  -0.953   0.215  1.00  0.00           C  
HETATM    6  C6  UNL     1      -2.139  -0.600  -1.228  1.00  0.00           C  
HETATM    7  C7  UNL     1      -3.276  -1.613   0.640  1.00  0.00           C  
HETATM    8  C8  UNL     1      -0.888  -1.972   0.471  1.00  0.00           C  
HETATM    9  C9  UNL     1       0.214  -2.277  -0.113  1.00  0.00           C  
HETATM   10  C10 UNL     1       0.906  -1.733  -1.296  1.00  0.00           C  
HETATM   11  C11 UNL     1       2.016  -0.719  -0.899  1.00  0.00           C  
HETATM   12  C12 UNL     1       3.125  -1.445  -0.172  1.00  0.00           C  
HETATM   13  O1  UNL     1       2.423  -0.130  -2.077  1.00  0.00           O  
HETATM   14  C13 UNL     1       1.315   0.228  -0.007  1.00  0.00           C  
HETATM   15  C14 UNL     1       2.005   1.388   0.601  1.00  0.00           C  
HETATM   16  C15 UNL     1       0.830   2.020   1.398  1.00  0.00           C  
HETATM   17  H1  UNL     1      -1.113   3.674  -0.901  1.00  0.00           H  
HETATM   18  H2  UNL     1       0.715   3.397  -0.935  1.00  0.00           H  
HETATM   19  H3  UNL     1      -0.012   4.317   0.406  1.00  0.00           H  
HETATM   20  H4  UNL     1      -2.223   1.839  -0.287  1.00  0.00           H  
HETATM   21  H5  UNL     1      -2.783   0.483   1.664  1.00  0.00           H  
HETATM   22  H6  UNL     1      -1.120  -0.012   1.955  1.00  0.00           H  
HETATM   23  H7  UNL     1      -1.560   0.228  -1.615  1.00  0.00           H  
HETATM   24  H8  UNL     1      -3.227  -0.294  -1.375  1.00  0.00           H  
HETATM   25  H9  UNL     1      -2.045  -1.485  -1.888  1.00  0.00           H  
HETATM   26  H10 UNL     1      -3.655  -2.255  -0.157  1.00  0.00           H  
HETATM   27  H11 UNL     1      -3.978  -0.817   0.940  1.00  0.00           H  
HETATM   28  H12 UNL     1      -3.028  -2.177   1.577  1.00  0.00           H  
HETATM   29  H13 UNL     1      -1.143  -2.582   1.383  1.00  0.00           H  
HETATM   30  H14 UNL     1       0.797  -3.128   0.344  1.00  0.00           H  
HETATM   31  H15 UNL     1       1.467  -2.506  -1.859  1.00  0.00           H  
HETATM   32  H16 UNL     1       0.295  -1.201  -2.018  1.00  0.00           H  
HETATM   33  H17 UNL     1       3.085  -1.204   0.919  1.00  0.00           H  
HETATM   34  H18 UNL     1       2.958  -2.556  -0.234  1.00  0.00           H  
HETATM   35  H19 UNL     1       4.121  -1.166  -0.611  1.00  0.00           H  
HETATM   36  H20 UNL     1       3.420  -0.082  -2.082  1.00  0.00           H  
HETATM   37  H21 UNL     1       0.539   0.688  -0.648  1.00  0.00           H  
HETATM   38  H22 UNL     1       0.955  -0.386   0.838  1.00  0.00           H  
HETATM   39  H23 UNL     1       2.764   1.151   1.345  1.00  0.00           H  
HETATM   40  H24 UNL     1       2.292   2.174  -0.124  1.00  0.00           H  
HETATM   41  H25 UNL     1       0.545   1.281   2.170  1.00  0.00           H  
HETATM   42  H26 UNL     1       1.168   2.927   1.899  1.00  0.00           H  
CONECT    1    2   17   18   19
CONECT    2    3    3   16
CONECT    3    4   20
CONECT    4    5   21   22
CONECT    5    6    7    8
CONECT    6   23   24   25
CONECT    7   26   27   28
CONECT    8    9    9   29
CONECT    9   10   30
CONECT   10   11   31   32
CONECT   11   12   13   14
CONECT   12   33   34   35
CONECT   13   36
CONECT   14   15   37   38
CONECT   15   16   39   40
CONECT   16   41   42
END

HMDB0038213
     RDKit          3D
Humulol
 42 42  0  0  0  0  0  0  0  0999 V2000
   -0.2144    3.4930   -0.3115 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3612    2.2336    0.5297 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4379    1.5053    0.4263 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8182    0.2618    1.1166 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9352   -0.9530    0.2151 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1388   -0.6004   -1.2285 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2763   -1.6129    0.6401 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8879   -1.9723    0.4710 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2137   -2.2770   -0.1130 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9061   -1.7327   -1.2963 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0159   -0.7187   -0.8986 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1252   -1.4446   -0.1722 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4232   -0.1297   -2.0768 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3152    0.2280   -0.0069 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0052    1.3884    0.6014 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8299    2.0204    1.3984 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1129    3.6738   -0.9013 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    3.3967   -0.9353 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0124    4.3173    0.4056 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2233    1.8394   -0.2869 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7828    0.4825    1.6639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1196   -0.0118    1.9547 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5599    0.2283   -1.6155 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2266   -0.2942   -1.3749 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0455   -1.4852   -1.8880 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6550   -2.2545   -0.1567 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9781   -0.8168    0.9399 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0281   -2.1769    1.5767 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1428   -2.5819    1.3826 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7973   -3.1276    0.3439 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4668   -2.5062   -1.8592 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2948   -1.2013   -2.0185 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0850   -1.2039    0.9195 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9583   -2.5560   -0.2335 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1206   -1.1657   -0.6112 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4202   -0.0816   -2.0817 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5395    0.6884   -0.6482 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9554   -0.3858    0.8383 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7638    1.1514    1.3447 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2924    2.1742   -0.1237 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5454    1.2811    2.1703 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1681    2.9267    1.8993 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
  5  7  1  0
  5  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 11 13  1  0
 11 14  1  0
 14 15  1  0
 15 16  1  0
 16  2  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  3 20  1  0
  4 21  1  0
  4 22  1  0
  6 23  1  0
  6 24  1  0
  6 25  1  0
  7 26  1  0
  7 27  1  0
  7 28  1  0
  8 29  1  0
  9 30  1  0
 10 31  1  0
 10 32  1  0
 12 33  1  0
 12 34  1  0
 12 35  1  0
 13 36  1  0
 14 37  1  0
 14 38  1  0
 15 39  1  0
 15 40  1  0
 16 41  1  0
 16 42  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₁₅H₂₆O

Average Molecular Weight

222.3663

Monoisotopic Molecular Weight

222.198365454

IUPAC Name

(3E,7E)-1,5,5,8-tetramethylcycloundeca-3,7-dien-1-ol

Traditional Name

(3E,7E)-1,5,5,8-tetramethylcycloundeca-3,7-dien-1-ol

CAS Registry Number

24405-58-1

SMILES

C\C1=C/CC(C)(C)\C=C\CC(C)(O)CCC1

InChI Identifier

InChI=1S/C15H26O/c1-13-7-5-10-15(4,16)11-6-9-14(2,3)12-8-13/h6,8-9,16H,5,7,10-12H2,1-4H3/b9-6+,13-8+

InChI Key

ZLMAVMBYWKVCLV-IMWXLZLDSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Sesquiterpenoids

Alternative Parents

Substituents

Humulane sesquiterpenoid
Sesquiterpenoid
Tertiary alcohol
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Alcohol
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic homomonocyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Route of exposure

Enteral

Ingestion (HMDB: HMDB0038213)

Source

Endogenous

Endogenous (HMDB: HMDB0038213)

Animal

Animal (HMDB: HMDB0038213)

Exogenous

Food

Food (HMDB: HMDB0038213)

Beverage

Alcoholic beverage

Alcoholic beverages (FooDB: FOOD00854)

Fat and oil

Fats and oils (FooDB: FOOD00864)

Exogenous (HMDB: HMDB0038213)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid Peroxidation (HMDB: HMDB0038213)

Biochemical pathway

Metabolic pathway

Fatty Acid Metabolism (HMDB: HMDB0038213)

Lipid metabolism pathway (HMDB: HMDB0038213)

Cellular process

Cell signaling (HMDB: HMDB0038213)

Biochemical process

Lipid transport (HMDB: HMDB0038213)

Role

Biological role

Energy source (HMDB: HMDB0038213)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0038213)

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	0.035 g/L	ALOGPS
logP	5.04	ALOGPS
logP	3.89	ChemAxon
logS	-3.8	ALOGPS
pKa (Strongest Acidic)	19.3	ChemAxon
pKa (Strongest Basic)	-0.92	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	72.46 m³·mol⁻¹	ChemAxon
Polarizability	27.58 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	155.552	31661259
DarkChem	[M-H]-	150.293	31661259
DeepCCS	[M+H]+	160.495	30932474
DeepCCS	[M-H]-	158.137	30932474
DeepCCS	[M-2H]-	191.058	30932474
DeepCCS	[M+Na]+	166.589	30932474
AllCCS	[M+H]+	152.2	32859911
AllCCS	[M+H-H2O]+	148.3	32859911
AllCCS	[M+NH4]+	155.8	32859911
AllCCS	[M+Na]+	156.9	32859911
AllCCS	[M-H]-	159.6	32859911
AllCCS	[M+Na-2H]-	160.4	32859911
AllCCS	[M+HCOO]-	161.5	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Humulol	C\C1=C/CC(C)(C)\C=C\CC(C)(O)CCC1	2167.6	Standard polar	33892256
Humulol	C\C1=C/CC(C)(C)\C=C\CC(C)(O)CCC1	1577.6	Standard non polar	33892256
Humulol	C\C1=C/CC(C)(C)\C=C\CC(C)(O)CCC1	1615.4	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Humulol,1TMS,isomer #1	C/C1=C\CC(C)(C)/C=C/CC(C)(O[Si](C)(C)C)CCC1	1721.6	Semi standard non polar	33892256
Humulol,1TBDMS,isomer #1	C/C1=C\CC(C)(C)/C=C/CC(C)(O[Si](C)(C)C(C)(C)C)CCC1	1962.0	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 - Humulol GC-MS (Non-derivatized) - 70eV, Positive	splash10-0a4i-0390000000-9b29df162ca24abda9c6	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Humulol GC-MS (1 TMS) - 70eV, Positive	splash10-00bi-9060000000-b7f093c98d8f4af2d6c9	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Humulol 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 - Humulol 10V, Positive-QTOF	splash10-0ab9-0090000000-5a34e569b1dabc3b3554	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Humulol 20V, Positive-QTOF	splash10-0ab9-3790000000-88646818f07025198518	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Humulol 40V, Positive-QTOF	splash10-067i-9600000000-f5fae16390faeba751d4	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Humulol 10V, Negative-QTOF	splash10-00di-0090000000-276592676d8cb86a7c40	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Humulol 20V, Negative-QTOF	splash10-00di-0190000000-4934bab88b17f5e372e6	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Humulol 40V, Negative-QTOF	splash10-06vi-2910000000-ce3db01ae1b0de39df26	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Humulol 10V, Negative-QTOF	splash10-00di-0090000000-ab61d8a2af41e6ed2e49	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Humulol 20V, Negative-QTOF	splash10-00di-0090000000-ab61d8a2af41e6ed2e49	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Humulol 40V, Negative-QTOF	splash10-00di-0090000000-b61a2d1787c8da89fffe	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Humulol 10V, Positive-QTOF	splash10-0a4i-0090000000-c084f3d998cc56a199d6	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Humulol 20V, Positive-QTOF	splash10-0a4i-0090000000-960a7984b5f2726bf34a	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Humulol 40V, Positive-QTOF	splash10-0a4r-0890000000-e780ce8ae2abafeb4b38	2021-09-24	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

FDB017455

KNApSAcK ID

Not Available

Chemspider ID

30772421

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

14093951

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

rw1027241

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.. .
(). Peacock VE, Deinzer ML, McGill LA, Wrolstad RE. Hop aroma in American beer. Journal of Agricultural and Food Chemistry 1980 Jul;28(4):774-777. [Structure]. .
Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.

Showing metabocard for Humulol (HMDB0038213)

MOL for HMDB0038213 (Humulol)

3D MOL for HMDB0038213 (Humulol)

3D SDF for HMDB0038213 (Humulol)

3D-SDF for HMDB0038213 (Humulol)

PDB for HMDB0038213 (Humulol)

3D PDB for HMDB0038213 (Humulol)

SMILES for HMDB0038213 (Humulol)

INCHI for HMDB0038213 (Humulol)

Structure for HMDB0038213 (Humulol)

3D Structure for HMDB0038213 (Humulol)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra