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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 21:48:29 UTC

Update Date

2022-03-07 02:55:00 UTC

HMDB ID

HMDB0036645

Secondary Accession Numbers

HMDB36645

Metabolite Identification

Common Name

Globulol

Description

Globulol belongs to the class of organic compounds known as 5,10-cycloaromadendrane sesquiterpenoids. These are aromadendrane sesquiterpenoids that arise from the C5-C10 cyclization of the aromadendrane skeleton. Based on a literature review a small amount of articles have been published on Globulol.

Structure

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

HMDB0036645
     RDKit          3D
Globulol
 42 44  0  0  0  0  0  0  0  0999 V2000
    0.2317   -3.2212   -0.0113 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1037   -1.8086   -0.5226 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4826   -1.9724   -1.1892 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0089   -0.5629   -1.1474 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5674   -0.0547    0.2079 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3031   -0.8195    0.5624 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8068    0.0005    1.0503 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1970    1.2135    0.3204 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6327    1.4796   -1.0053 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7627    2.0818   -0.8647 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4529    1.4209    0.2666 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8890    1.9751    0.2891 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8786    1.8309    1.4508 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1722    0.1151    0.6145 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2385    0.3993    1.7010 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7990   -0.5053   -0.5903 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0119   -3.9683   -0.7783 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4953   -3.3969    0.8321 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2457   -3.2760    0.3891 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5835   -1.6182   -1.3152 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3566   -2.3440   -2.2404 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1213   -2.6562   -0.6139 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1344   -0.6539   -1.2152 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7139    0.0636   -1.9857 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4312   -0.3178    0.8948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6338   -1.4996    1.4219 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6634    0.2381    2.1656 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4324    2.1786    0.8737 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2455    2.3087   -1.4765 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5782    0.7144   -1.7529 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6477    3.1608   -0.6110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3136    2.0571   -1.8257 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5565    1.2198    0.7362 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1969    2.2816   -0.7308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9447    2.8784    0.9354 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4253    1.4690    2.1935 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7420    0.5576    2.6637 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7095    1.3602    1.3906 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9984   -0.3840    1.6841 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8484   -1.6197   -0.5520 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8912   -0.2066   -0.6515 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4160   -0.1188   -1.5638 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
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 11 13  1  0
  8 14  1  0
 14 15  1  0
 14 16  1  0
  6  2  1  0
 14  7  1  0
 11  5  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  2 20  1  0
  3 21  1  0
  3 22  1  0
  4 23  1  0
  4 24  1  0
  5 25  1  0
  6 26  1  0
  7 27  1  0
  8 28  1  0
  9 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
 15 37  1  0
 15 38  1  0
 15 39  1  0
 16 40  1  0
 16 41  1  0
 16 42  1  0
M  END


  Mrv0541 02241215192D          

 16 18  0  0  0  0            999 V2000
    0.2888   -1.8570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2888   -1.1965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7012   -1.9392    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0314   -0.9485    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4438   -0.2058    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1136    0.5360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2888    0.7012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2888    0.2058    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2888   -0.6190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1136   -0.8663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6090   -0.2058    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1136    0.4539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3616    1.2787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3709    1.9392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8663    1.2787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6090    1.6090    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
  2  4  1  0  0  0  0
  2  9  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6 15  1  0  0  0  0
  7  8  1  0  0  0  0
  7 15  1  0  0  0  0
  8  9  1  0  0  0  0
  8 12  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
 12 13  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0036645

> <DATABASE_NAME>
hmdb

> <SMILES>
CC1CCC2C1C1C(CCC2(C)O)C1(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C15H26O/c1-9-5-6-10-12(9)13-11(14(13,2)3)7-8-15(10,4)16/h9-13,16H,5-8H2,1-4H3

> <INCHI_KEY>
AYXPYQRXGNDJFU-UHFFFAOYSA-N

> <FORMULA>
C15H26O

> <MOLECULAR_WEIGHT>
222.3663

> <EXACT_MASS>
222.198365454

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_AVERAGE_POLARIZABILITY>
27.440621840390012

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1,1,2,5-tetramethyl-decahydro-1H-cyclopropa[e]azulen-5-ol

> <ALOGPS_LOGP>
3.15

> <JCHEM_LOGP>
3.1785024189999995

> <ALOGPS_LOGS>
-4.72

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-0.5138122997029483

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
66.60000000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.27e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
ledol

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0036645
     RDKit          3D
Globulol
 42 44  0  0  0  0  0  0  0  0999 V2000
    0.2317   -3.2212   -0.0113 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1037   -1.8086   -0.5226 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4826   -1.9724   -1.1892 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0089   -0.5629   -1.1474 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5674   -0.0547    0.2079 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3031   -0.8195    0.5624 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8068    0.0005    1.0503 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1970    1.2135    0.3204 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6327    1.4796   -1.0053 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7627    2.0818   -0.8647 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4529    1.4209    0.2666 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8890    1.9751    0.2891 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8786    1.8309    1.4508 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1722    0.1151    0.6145 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2385    0.3993    1.7010 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7990   -0.5053   -0.5903 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0119   -3.9683   -0.7783 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4953   -3.3969    0.8321 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2457   -3.2760    0.3891 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5835   -1.6182   -1.3152 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3566   -2.3440   -2.2404 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1213   -2.6562   -0.6139 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1344   -0.6539   -1.2152 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7139    0.0636   -1.9857 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4312   -0.3178    0.8948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6338   -1.4996    1.4219 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6634    0.2381    2.1656 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4324    2.1786    0.8737 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2455    2.3087   -1.4765 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5782    0.7144   -1.7529 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6477    3.1608   -0.6110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3136    2.0571   -1.8257 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5565    1.2198    0.7362 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1969    2.2816   -0.7308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9447    2.8784    0.9354 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4253    1.4690    2.1935 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7420    0.5576    2.6637 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7095    1.3602    1.3906 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9984   -0.3840    1.6841 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8484   -1.6197   -0.5520 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8912   -0.2066   -0.6515 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4160   -0.1188   -1.5638 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
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 11 13  1  0
  8 14  1  0
 14 15  1  0
 14 16  1  0
  6  2  1  0
 14  7  1  0
 11  5  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  2 20  1  0
  3 21  1  0
  3 22  1  0
  4 23  1  0
  4 24  1  0
  5 25  1  0
  6 26  1  0
  7 27  1  0
  8 28  1  0
  9 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
 15 37  1  0
 15 38  1  0
 15 39  1  0
 16 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       0.539  -3.466   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.539  -2.233   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -1.309  -3.620   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      -1.925  -1.771   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.695  -0.384   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.079   1.001   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.539   1.309   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.539   0.384   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.539  -1.155   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.079  -1.617   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.003  -0.384   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.079   0.847   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.542   2.387   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.692   3.620   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.617   2.387   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -3.003   3.003   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4    9                                             
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   15                                                  
CONECT    7    6    8   15                                                  
CONECT    8    7    9   12                                                  
CONECT    9    2    8   10                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12    8   11   13                                                  
CONECT   13   12                                                            
CONECT   14   15                                                            
CONECT   15    6    7   14   16                                             
CONECT   16   15                                                            
MASTER        0    0    0    0    0    0    0    0   16    0   36    0
END

COMPND    HMDB0036645
HETATM    1  C1  UNL     1       0.232  -3.221  -0.011  1.00  0.00           C  
HETATM    2  C2  UNL     1      -0.104  -1.809  -0.523  1.00  0.00           C  
HETATM    3  C3  UNL     1      -1.483  -1.972  -1.189  1.00  0.00           C  
HETATM    4  C4  UNL     1      -2.009  -0.563  -1.147  1.00  0.00           C  
HETATM    5  C5  UNL     1      -1.567  -0.055   0.208  1.00  0.00           C  
HETATM    6  C6  UNL     1      -0.303  -0.820   0.562  1.00  0.00           C  
HETATM    7  C7  UNL     1       0.807   0.001   1.050  1.00  0.00           C  
HETATM    8  C8  UNL     1       1.197   1.214   0.320  1.00  0.00           C  
HETATM    9  C9  UNL     1       0.633   1.480  -1.005  1.00  0.00           C  
HETATM   10  C10 UNL     1      -0.763   2.082  -0.865  1.00  0.00           C  
HETATM   11  C11 UNL     1      -1.453   1.421   0.267  1.00  0.00           C  
HETATM   12  C12 UNL     1      -2.889   1.975   0.289  1.00  0.00           C  
HETATM   13  O1  UNL     1      -0.879   1.831   1.451  1.00  0.00           O  
HETATM   14  C13 UNL     1       2.172   0.115   0.615  1.00  0.00           C  
HETATM   15  C14 UNL     1       3.239   0.399   1.701  1.00  0.00           C  
HETATM   16  C15 UNL     1       2.799  -0.505  -0.590  1.00  0.00           C  
HETATM   17  H1  UNL     1      -0.012  -3.968  -0.778  1.00  0.00           H  
HETATM   18  H2  UNL     1      -0.495  -3.397   0.832  1.00  0.00           H  
HETATM   19  H3  UNL     1       1.246  -3.276   0.389  1.00  0.00           H  
HETATM   20  H4  UNL     1       0.584  -1.618  -1.315  1.00  0.00           H  
HETATM   21  H5  UNL     1      -1.357  -2.344  -2.240  1.00  0.00           H  
HETATM   22  H6  UNL     1      -2.121  -2.656  -0.614  1.00  0.00           H  
HETATM   23  H7  UNL     1      -3.134  -0.654  -1.215  1.00  0.00           H  
HETATM   24  H8  UNL     1      -1.714   0.064  -1.986  1.00  0.00           H  
HETATM   25  H9  UNL     1      -2.431  -0.318   0.895  1.00  0.00           H  
HETATM   26  H10 UNL     1      -0.634  -1.500   1.422  1.00  0.00           H  
HETATM   27  H11 UNL     1       0.663   0.238   2.166  1.00  0.00           H  
HETATM   28  H12 UNL     1       1.432   2.179   0.874  1.00  0.00           H  
HETATM   29  H13 UNL     1       1.245   2.309  -1.477  1.00  0.00           H  
HETATM   30  H14 UNL     1       0.578   0.714  -1.753  1.00  0.00           H  
HETATM   31  H15 UNL     1      -0.648   3.161  -0.611  1.00  0.00           H  
HETATM   32  H16 UNL     1      -1.314   2.057  -1.826  1.00  0.00           H  
HETATM   33  H17 UNL     1      -3.557   1.220   0.736  1.00  0.00           H  
HETATM   34  H18 UNL     1      -3.197   2.282  -0.731  1.00  0.00           H  
HETATM   35  H19 UNL     1      -2.945   2.878   0.935  1.00  0.00           H  
HETATM   36  H20 UNL     1      -1.425   1.469   2.193  1.00  0.00           H  
HETATM   37  H21 UNL     1       2.742   0.558   2.664  1.00  0.00           H  
HETATM   38  H22 UNL     1       3.710   1.360   1.391  1.00  0.00           H  
HETATM   39  H23 UNL     1       3.998  -0.384   1.684  1.00  0.00           H  
HETATM   40  H24 UNL     1       2.848  -1.620  -0.552  1.00  0.00           H  
HETATM   41  H25 UNL     1       3.891  -0.207  -0.651  1.00  0.00           H  
HETATM   42  H26 UNL     1       2.416  -0.119  -1.564  1.00  0.00           H  
CONECT    1    2   17   18   19
CONECT    2    3    6   20
CONECT    3    4   21   22
CONECT    4    5   23   24
CONECT    5    6   11   25
CONECT    6    7   26
CONECT    7    8   14   27
CONECT    8    9   14   28
CONECT    9   10   29   30
CONECT   10   11   31   32
CONECT   11   12   13
CONECT   12   33   34   35
CONECT   13   36
CONECT   14   15   16
CONECT   15   37   38   39
CONECT   16   40   41   42
END

HMDB0036645
     RDKit          3D
Globulol
 42 44  0  0  0  0  0  0  0  0999 V2000
    0.2317   -3.2212   -0.0113 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1037   -1.8086   -0.5226 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4826   -1.9724   -1.1892 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0089   -0.5629   -1.1474 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5674   -0.0547    0.2079 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3031   -0.8195    0.5624 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8068    0.0005    1.0503 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1970    1.2135    0.3204 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6327    1.4796   -1.0053 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7627    2.0818   -0.8647 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4529    1.4209    0.2666 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8890    1.9751    0.2891 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8786    1.8309    1.4508 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1722    0.1151    0.6145 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2385    0.3993    1.7010 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7990   -0.5053   -0.5903 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0119   -3.9683   -0.7783 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4953   -3.3969    0.8321 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2457   -3.2760    0.3891 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5835   -1.6182   -1.3152 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3566   -2.3440   -2.2404 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1213   -2.6562   -0.6139 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1344   -0.6539   -1.2152 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7139    0.0636   -1.9857 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4312   -0.3178    0.8948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6338   -1.4996    1.4219 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6634    0.2381    2.1656 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4324    2.1786    0.8737 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2455    2.3087   -1.4765 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5782    0.7144   -1.7529 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6477    3.1608   -0.6110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3136    2.0571   -1.8257 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5565    1.2198    0.7362 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1969    2.2816   -0.7308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9447    2.8784    0.9354 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4253    1.4690    2.1935 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7420    0.5576    2.6637 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7095    1.3602    1.3906 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9984   -0.3840    1.6841 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8484   -1.6197   -0.5520 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8912   -0.2066   -0.6515 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4160   -0.1188   -1.5638 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
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 11 13  1  0
  8 14  1  0
 14 15  1  0
 14 16  1  0
  6  2  1  0
 14  7  1  0
 11  5  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  2 20  1  0
  3 21  1  0
  3 22  1  0
  4 23  1  0
  4 24  1  0
  5 25  1  0
  6 26  1  0
  7 27  1  0
  8 28  1  0
  9 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
 15 37  1  0
 15 38  1  0
 15 39  1  0
 16 40  1  0
 16 41  1  0
 16 42  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
1,1,4,7-Tetramethyldecahydro-1H-cyclopropa(e)azulen-4-ol	MeSH
(-)-Globulol	HMDB
Epiglobulol	HMDB
Globulol	MeSH

Chemical Formula

C₁₅H₂₆O

Average Molecular Weight

222.3663

Monoisotopic Molecular Weight

222.198365454

IUPAC Name

1,1,2,5-tetramethyl-decahydro-1H-cyclopropa[e]azulen-5-ol

Traditional Name

ledol

CAS Registry Number

489-41-8

SMILES

CC1CCC2C1C1C(CCC2(C)O)C1(C)C

InChI Identifier

InChI=1S/C15H26O/c1-9-5-6-10-12(9)13-11(14(13,2)3)7-8-15(10,4)16/h9-13,16H,5-8H2,1-4H3

InChI Key

AYXPYQRXGNDJFU-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 5,10-cycloaromadendrane sesquiterpenoids. These are aromadendrane sesquiterpenoids that arise from the C5-C10 cyclization of the aromadendrane skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

5,10-cycloaromadendrane sesquiterpenoids

Alternative Parents

Substituents

5,10-cycloaromadendrane sesquiterpenoid
Guaiane sesquiterpenoid
Tertiary alcohol
Cyclic alcohol
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

a sesquiterpenoid (CPD-13864 )

Ontology

Sweet

Disposition

Source

Exogenous

Exogenous (HMDB: HMDB0036645)

Not Available

EC 3.1.1.7 (acetylcholinesterase) inhibitor (HMDB: HMDB0036645)

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	88.5 °C	Not Available
Boiling Point	293.00 to 294.00 °C. @ 760.00 mm Hg	The Good Scents Company Information System
Water Solubility	11.98 mg/L @ 25 °C (est)	The Good Scents Company Information System
LogP	4.807 (est)	The Good Scents Company Information System

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.0043 g/L	ALOGPS
logP	3.15	ALOGPS
logP	3.18	ChemAxon
logS	-4.7	ALOGPS
pKa (Strongest Basic)	-0.51	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	66.6 m³·mol⁻¹	ChemAxon
Polarizability	27.44 Å³	ChemAxon
Number of Rings	3	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]+	154.195	31661259
DarkChem	[M-H]-	148.219	31661259
DeepCCS	[M+H]+	158.263	30932474
DeepCCS	[M-H]-	155.905	30932474
DeepCCS	[M-2H]-	189.17	30932474
DeepCCS	[M+Na]+	164.357	30932474
AllCCS	[M+H]+	152.0	32859911
AllCCS	[M+H-H2O]+	148.3	32859911
AllCCS	[M+NH4]+	155.5	32859911
AllCCS	[M+Na]+	156.5	32859911
AllCCS	[M-H]-	162.0	32859911
AllCCS	[M+Na-2H]-	162.3	32859911
AllCCS	[M+HCOO]-	162.9	32859911

Predicted Retention Times

Underivatized

Chromatographic Method	Retention Time	Reference
Measured using a Waters Acquity ultraperformance liquid chromatography (UPLC) ethylene-bridged hybrid (BEH) C18 column (100 mm × 2.1 mm; 1.7 μmparticle diameter). Predicted by Afia on May 17, 2022. Predicted by Afia on May 17, 2022.	4.79 minutes	32390414
Predicted by Siyang on May 30, 2022	16.5688 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	2.33 minutes	32390414
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	2418.3 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	513.8 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	199.2 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	224.9 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	400.1 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	770.3 seconds	40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid	794.2 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	98.8 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	1233.3 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	453.9 seconds	40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid	1444.7 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	452.3 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	415.6 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	416.8 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	554.8 seconds	40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water	11.7 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Globulol	CC1CCC2C1C1C(CCC2(C)O)C1(C)C	2069.7	Standard polar	33892256
Globulol	CC1CCC2C1C1C(CCC2(C)O)C1(C)C	1605.0	Standard non polar	33892256
Globulol	CC1CCC2C1C1C(CCC2(C)O)C1(C)C	1580.8	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Globulol,1TMS,isomer #1	CC1CCC2C1C1C(CCC2(C)O[Si](C)(C)C)C1(C)C	1744.2	Semi standard non polar	33892256
Globulol,1TBDMS,isomer #1	CC1CCC2C1C1C(CCC2(C)O[Si](C)(C)C(C)(C)C)C1(C)C	1988.2	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 - Globulol GC-MS (Non-derivatized) - 70eV, Positive	splash10-055f-5920000000-7ef3a26b7fce9bffa490	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Globulol GC-MS (1 TMS) - 70eV, Positive	splash10-0g30-6290000000-d77bfb80d0e5077bf1be	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Globulol GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Globulol 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 - Globulol 10V, Positive-QTOF	splash10-0ab9-0190000000-818c3dc968292e862a64	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Globulol 20V, Positive-QTOF	splash10-0ab9-1490000000-76d7331c7da8828ba7c6	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Globulol 40V, Positive-QTOF	splash10-0a5i-9700000000-44c2d74c65cbeede481b	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Globulol 10V, Positive-QTOF	splash10-0ab9-0190000000-818c3dc968292e862a64	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Globulol 20V, Positive-QTOF	splash10-0ab9-1490000000-76d7331c7da8828ba7c6	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Globulol 40V, Positive-QTOF	splash10-0a5i-9700000000-44c2d74c65cbeede481b	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Globulol 10V, Positive-QTOF	splash10-0ab9-0190000000-818c3dc968292e862a64	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Globulol 20V, Positive-QTOF	splash10-0ab9-1490000000-76d7331c7da8828ba7c6	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Globulol 40V, Positive-QTOF	splash10-0a5i-9700000000-44c2d74c65cbeede481b	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Globulol 10V, Negative-QTOF	splash10-00di-0090000000-afd2ae90f4931c90658a	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Globulol 20V, Negative-QTOF	splash10-00di-0090000000-bf9ea772ff8b2aac4e15	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Globulol 40V, Negative-QTOF	splash10-01t9-4920000000-83420d48c4c1d0961770	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Globulol 10V, Negative-QTOF	splash10-00di-0090000000-afd2ae90f4931c90658a	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Globulol 20V, Negative-QTOF	splash10-00di-0090000000-bf9ea772ff8b2aac4e15	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Globulol 40V, Negative-QTOF	splash10-01t9-4920000000-83420d48c4c1d0961770	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Globulol 10V, Negative-QTOF	splash10-00di-0090000000-afd2ae90f4931c90658a	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Globulol 20V, Negative-QTOF	splash10-00di-0090000000-bf9ea772ff8b2aac4e15	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Globulol 40V, Negative-QTOF	splash10-01t9-4920000000-83420d48c4c1d0961770	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Globulol 10V, Positive-QTOF	splash10-00di-2090000000-0f255fbffb27c85c9982	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Globulol 20V, Positive-QTOF	splash10-0a59-9820000000-ffe7643b408e312aa1f3	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Globulol 40V, Positive-QTOF	splash10-05o3-9000000000-98d81875a3a25376c251	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Globulol 10V, Negative-QTOF	splash10-00di-0090000000-ab61d8a2af41e6ed2e49	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Globulol 20V, Negative-QTOF	splash10-00di-0090000000-ab61d8a2af41e6ed2e49	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Globulol 40V, Negative-QTOF	splash10-00di-0090000000-ab61d8a2af41e6ed2e49	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

FDB015567

KNApSAcK ID

C00003161

Chemspider ID

91904

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

101716

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

rw1384371

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 Globulol (HMDB0036645)

MOL for HMDB0036645 (Globulol)

3D MOL for HMDB0036645 (Globulol)

3D SDF for HMDB0036645 (Globulol)

3D-SDF for HMDB0036645 (Globulol)

PDB for HMDB0036645 (Globulol)

3D PDB for HMDB0036645 (Globulol)

SMILES for HMDB0036645 (Globulol)

INCHI for HMDB0036645 (Globulol)

Structure for HMDB0036645 (Globulol)

3D Structure for HMDB0036645 (Globulol)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra