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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 23:28:39 UTC

Update Date

2022-03-07 02:55:40 UTC

HMDB ID

HMDB0038197

Secondary Accession Numbers

HMDB38197

Metabolite Identification

Common Name

alpha-Bisabolol oxide B

Description

alpha-Bisabolol oxide B, also known as α-bisabolol oxide b, belongs to the class of organic compounds known as tetrahydrofurans. These are heterocyclic compounds containing a saturated, aliphatic, five-membered ring where a carbon is replaced by an oxygen. alpha-Bisabolol oxide B has been detected, but not quantified in, several different foods, such as black tea, green tea, herbal tea, herbs and spices, and teas (Camellia sinensis). This could make alpha-bisabolol oxide b a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on alpha-Bisabolol oxide B.

Structure

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

HMDB0038197
     RDKit          3D
alpha-Bisabolol oxide B
 43 44  0  0  0  0  0  0  0  0999 V2000
    4.9337    1.8178    0.2544 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6342    1.0895    0.2213 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5336    1.6977    0.6293 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1906    1.0833    0.6443 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2464   -0.2163   -0.0884 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0367   -1.0033   -0.0086 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1449   -2.2875   -0.7831 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4698   -1.2858    1.3861 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8542   -0.6238    1.4249 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2060   -0.6208   -0.0385 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2954    0.3686   -0.3702 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6183   -0.0536    0.2080 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9383    1.7736    0.0106 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4318    0.3497   -1.7738 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0224   -0.2674   -0.6388 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4502   -1.0026    0.3516 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6655   -0.3128   -0.2831 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7482    2.9249    0.3439 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5355    1.4678    1.1342 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4998    1.5828   -0.6763 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6242    2.7297    0.9807 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8223    0.9973    1.6812 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5229    1.7679    0.0448 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3927    0.0322   -1.1806 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8073   -2.5941   -1.3025 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4501   -3.0940   -0.0621 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8946   -2.1354   -1.5573 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1907   -0.8941    2.1718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6626   -2.3881    1.5006 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5566   -1.2614    2.0166 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7091    0.3650    1.8587 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5385   -1.6264   -0.3080 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4023    0.6170   -0.2226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7749   -1.1175   -0.0666 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5727    0.0946    1.3022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9026    2.4698   -0.8683 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9503    1.8666    0.4990 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7256    2.2049    0.6787 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0504   -0.3815   -2.0277 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5983   -0.9670    1.4442 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4039   -2.0502   -0.0040 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5951   -0.8389   -0.0620 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4487   -0.2780   -1.3907 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 11 13  1  0
 11 14  1  0
 10 15  1  0
  5 16  1  0
 16 17  1  0
 17  2  1  0
 15  6  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  3 21  1  0
  4 22  1  0
  4 23  1  0
  5 24  1  0
  7 25  1  0
  7 26  1  0
  7 27  1  0
  8 28  1  0
  8 29  1  0
  9 30  1  0
  9 31  1  0
 10 32  1  0
 12 33  1  0
 12 34  1  0
 12 35  1  0
 13 36  1  0
 13 37  1  0
 13 38  1  0
 14 39  1  0
 16 40  1  0
 16 41  1  0
 17 42  1  0
 17 43  1  0
M  END


  Mrv0541 05061310172D          

 17 18  0  0  0  0            999 V2000
    5.0380    2.8876    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4475   -2.1692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5999   -1.9867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2778    1.0483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6790    2.4460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7409    1.4899    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1270    1.8329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1889    0.8768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2424   -0.8343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4973   -0.0497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4860    2.2745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3819    1.0483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4174   -0.8343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9324   -1.5018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8299    0.4352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2650   -1.0169    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1624   -0.0497    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  7  5  1  0  0  0  0
  8  6  1  0  0  0  0
 10  9  1  0  0  0  0
 11  1  1  0  0  0  0
 11  5  2  0  0  0  0
 11  6  1  0  0  0  0
 12  7  1  0  0  0  0
 12  8  1  0  0  0  0
 13  9  1  0  0  0  0
 14  2  1  0  0  0  0
 14  3  1  0  0  0  0
 14 13  1  0  0  0  0
 15  4  1  0  0  0  0
 15 10  1  0  0  0  0
 15 12  1  0  0  0  0
 16 14  1  0  0  0  0
 17 13  1  0  0  0  0
 17 15  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0038197

> <DATABASE_NAME>
hmdb

> <SMILES>
CC1=CCC(CC1)C1(C)CCC(O1)C(C)(C)O

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

> <INCHI_KEY>
RKBAYVATPNYHLW-UHFFFAOYSA-N

> <FORMULA>
C15H26O2

> <MOLECULAR_WEIGHT>
238.3657

> <EXACT_MASS>
238.193280076

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_AVERAGE_POLARIZABILITY>
28.853804684098368

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-[5-methyl-5-(4-methylcyclohex-3-en-1-yl)oxolan-2-yl]propan-2-ol

> <ALOGPS_LOGP>
3.56

> <JCHEM_LOGP>
2.9332302743333334

> <ALOGPS_LOGS>
-3.25

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.325328778261419

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0939011923884543

> <JCHEM_POLAR_SURFACE_AREA>
29.46

> <JCHEM_REFRACTIVITY>
71.025

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.35e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-[5-methyl-5-(4-methylcyclohex-3-en-1-yl)oxolan-2-yl]propan-2-ol

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0038197
     RDKit          3D
alpha-Bisabolol oxide B
 43 44  0  0  0  0  0  0  0  0999 V2000
    4.9337    1.8178    0.2544 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6342    1.0895    0.2213 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5336    1.6977    0.6293 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1906    1.0833    0.6443 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2464   -0.2163   -0.0884 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0367   -1.0033   -0.0086 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1449   -2.2875   -0.7831 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4698   -1.2858    1.3861 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8542   -0.6238    1.4249 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2060   -0.6208   -0.0385 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2954    0.3686   -0.3702 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6183   -0.0536    0.2080 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9383    1.7736    0.0106 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4318    0.3497   -1.7738 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0224   -0.2674   -0.6388 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4502   -1.0026    0.3516 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6655   -0.3128   -0.2831 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7482    2.9249    0.3439 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5355    1.4678    1.1342 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4998    1.5828   -0.6763 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6242    2.7297    0.9807 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8223    0.9973    1.6812 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5229    1.7679    0.0448 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3927    0.0322   -1.1806 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8073   -2.5941   -1.3025 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4501   -3.0940   -0.0621 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8946   -2.1354   -1.5573 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1907   -0.8941    2.1718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6626   -2.3881    1.5006 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5566   -1.2614    2.0166 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7091    0.3650    1.8587 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5385   -1.6264   -0.3080 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4023    0.6170   -0.2226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7749   -1.1175   -0.0666 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5727    0.0946    1.3022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9026    2.4698   -0.8683 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9503    1.8666    0.4990 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7256    2.2049    0.6787 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0504   -0.3815   -2.0277 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5983   -0.9670    1.4442 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4039   -2.0502   -0.0040 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5951   -0.8389   -0.0620 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4487   -0.2780   -1.3907 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 11 13  1  0
 11 14  1  0
 10 15  1  0
  5 16  1  0
 16 17  1  0
 17  2  1  0
 15  6  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  3 21  1  0
  4 22  1  0
  4 23  1  0
  5 24  1  0
  7 25  1  0
  7 26  1  0
  7 27  1  0
  8 28  1  0
  8 29  1  0
  9 30  1  0
  9 31  1  0
 10 32  1  0
 12 33  1  0
 12 34  1  0
 12 35  1  0
 13 36  1  0
 13 37  1  0
 13 38  1  0
 14 39  1  0
 16 40  1  0
 16 41  1  0
 17 42  1  0
 17 43  1  0
M  END

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0       9.404   5.390   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.702  -4.049   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.853  -3.709   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.252   1.957   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.867   4.566   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.850   2.781   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.837   3.421   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.819   1.637   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.052  -1.557   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.528  -0.093   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.374   4.246   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.313   1.957   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.512  -1.557   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.607  -2.803   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.282   0.812   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       2.361  -1.898   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       4.036  -0.093   0.000  0.00  0.00           O+0
CONECT    1   11                                                            
CONECT    2   14                                                            
CONECT    3   14                                                            
CONECT    4   15                                                            
CONECT    5    7   11                                                       
CONECT    6    8   11                                                       
CONECT    7    5   12                                                       
CONECT    8    6   12                                                       
CONECT    9   10   13                                                       
CONECT   10    9   15                                                       
CONECT   11    1    5    6                                                  
CONECT   12    7    8   15                                                  
CONECT   13    9   14   17                                                  
CONECT   14    2    3   13   16                                             
CONECT   15    4   10   12   17                                             
CONECT   16   14                                                            
CONECT   17   13   15                                                       
MASTER        0    0    0    0    0    0    0    0   17    0   36    0
END

COMPND    HMDB0038197
HETATM    1  C1  UNL     1       4.934   1.818   0.254  1.00  0.00           C  
HETATM    2  C2  UNL     1       3.634   1.090   0.221  1.00  0.00           C  
HETATM    3  C3  UNL     1       2.534   1.698   0.629  1.00  0.00           C  
HETATM    4  C4  UNL     1       1.191   1.083   0.644  1.00  0.00           C  
HETATM    5  C5  UNL     1       1.246  -0.216  -0.088  1.00  0.00           C  
HETATM    6  C6  UNL     1      -0.037  -1.003  -0.009  1.00  0.00           C  
HETATM    7  C7  UNL     1       0.145  -2.288  -0.783  1.00  0.00           C  
HETATM    8  C8  UNL     1      -0.470  -1.286   1.386  1.00  0.00           C  
HETATM    9  C9  UNL     1      -1.854  -0.624   1.425  1.00  0.00           C  
HETATM   10  C10 UNL     1      -2.206  -0.621  -0.038  1.00  0.00           C  
HETATM   11  C11 UNL     1      -3.295   0.369  -0.370  1.00  0.00           C  
HETATM   12  C12 UNL     1      -4.618  -0.054   0.208  1.00  0.00           C  
HETATM   13  C13 UNL     1      -2.938   1.774   0.011  1.00  0.00           C  
HETATM   14  O1  UNL     1      -3.432   0.350  -1.774  1.00  0.00           O  
HETATM   15  O2  UNL     1      -1.022  -0.267  -0.639  1.00  0.00           O  
HETATM   16  C14 UNL     1       2.450  -1.003   0.352  1.00  0.00           C  
HETATM   17  C15 UNL     1       3.665  -0.313  -0.283  1.00  0.00           C  
HETATM   18  H1  UNL     1       4.748   2.925   0.344  1.00  0.00           H  
HETATM   19  H2  UNL     1       5.536   1.468   1.134  1.00  0.00           H  
HETATM   20  H3  UNL     1       5.500   1.583  -0.676  1.00  0.00           H  
HETATM   21  H4  UNL     1       2.624   2.730   0.981  1.00  0.00           H  
HETATM   22  H5  UNL     1       0.822   0.997   1.681  1.00  0.00           H  
HETATM   23  H6  UNL     1       0.523   1.768   0.045  1.00  0.00           H  
HETATM   24  H7  UNL     1       1.393   0.032  -1.181  1.00  0.00           H  
HETATM   25  H8  UNL     1      -0.807  -2.594  -1.302  1.00  0.00           H  
HETATM   26  H9  UNL     1       0.450  -3.094  -0.062  1.00  0.00           H  
HETATM   27  H10 UNL     1       0.895  -2.135  -1.557  1.00  0.00           H  
HETATM   28  H11 UNL     1       0.191  -0.894   2.172  1.00  0.00           H  
HETATM   29  H12 UNL     1      -0.663  -2.388   1.501  1.00  0.00           H  
HETATM   30  H13 UNL     1      -2.557  -1.261   2.017  1.00  0.00           H  
HETATM   31  H14 UNL     1      -1.709   0.365   1.859  1.00  0.00           H  
HETATM   32  H15 UNL     1      -2.538  -1.626  -0.308  1.00  0.00           H  
HETATM   33  H16 UNL     1      -5.402   0.617  -0.223  1.00  0.00           H  
HETATM   34  H17 UNL     1      -4.775  -1.118  -0.067  1.00  0.00           H  
HETATM   35  H18 UNL     1      -4.573   0.095   1.302  1.00  0.00           H  
HETATM   36  H19 UNL     1      -2.903   2.470  -0.868  1.00  0.00           H  
HETATM   37  H20 UNL     1      -1.950   1.867   0.499  1.00  0.00           H  
HETATM   38  H21 UNL     1      -3.726   2.205   0.679  1.00  0.00           H  
HETATM   39  H22 UNL     1      -4.050  -0.381  -2.028  1.00  0.00           H  
HETATM   40  H23 UNL     1       2.598  -0.967   1.444  1.00  0.00           H  
HETATM   41  H24 UNL     1       2.404  -2.050  -0.004  1.00  0.00           H  
HETATM   42  H25 UNL     1       4.595  -0.839  -0.062  1.00  0.00           H  
HETATM   43  H26 UNL     1       3.449  -0.278  -1.391  1.00  0.00           H  
CONECT    1    2   18   19   20
CONECT    2    3    3   17
CONECT    3    4   21
CONECT    4    5   22   23
CONECT    5    6   16   24
CONECT    6    7    8   15
CONECT    7   25   26   27
CONECT    8    9   28   29
CONECT    9   10   30   31
CONECT   10   11   15   32
CONECT   11   12   13   14
CONECT   12   33   34   35
CONECT   13   36   37   38
CONECT   14   39
CONECT   16   17   40   41
CONECT   17   42   43
END

HMDB0038197
     RDKit          3D
alpha-Bisabolol oxide B
 43 44  0  0  0  0  0  0  0  0999 V2000
    4.9337    1.8178    0.2544 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6342    1.0895    0.2213 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5336    1.6977    0.6293 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1906    1.0833    0.6443 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2464   -0.2163   -0.0884 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0367   -1.0033   -0.0086 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1449   -2.2875   -0.7831 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4698   -1.2858    1.3861 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8542   -0.6238    1.4249 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2060   -0.6208   -0.0385 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2954    0.3686   -0.3702 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6183   -0.0536    0.2080 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9383    1.7736    0.0106 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4318    0.3497   -1.7738 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0224   -0.2674   -0.6388 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4502   -1.0026    0.3516 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6655   -0.3128   -0.2831 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7482    2.9249    0.3439 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5355    1.4678    1.1342 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4998    1.5828   -0.6763 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6242    2.7297    0.9807 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8223    0.9973    1.6812 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5229    1.7679    0.0448 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3927    0.0322   -1.1806 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8073   -2.5941   -1.3025 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4501   -3.0940   -0.0621 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8946   -2.1354   -1.5573 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1907   -0.8941    2.1718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6626   -2.3881    1.5006 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5566   -1.2614    2.0166 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7091    0.3650    1.8587 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5385   -1.6264   -0.3080 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4023    0.6170   -0.2226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7749   -1.1175   -0.0666 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5727    0.0946    1.3022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9026    2.4698   -0.8683 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9503    1.8666    0.4990 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7256    2.2049    0.6787 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0504   -0.3815   -2.0277 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5983   -0.9670    1.4442 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4039   -2.0502   -0.0040 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5951   -0.8389   -0.0620 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4487   -0.2780   -1.3907 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 11 13  1  0
 11 14  1  0
 10 15  1  0
  5 16  1  0
 16 17  1  0
 17  2  1  0
 15  6  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  3 21  1  0
  4 22  1  0
  4 23  1  0
  5 24  1  0
  7 25  1  0
  7 26  1  0
  7 27  1  0
  8 28  1  0
  8 29  1  0
  9 30  1  0
  9 31  1  0
 10 32  1  0
 12 33  1  0
 12 34  1  0
 12 35  1  0
 13 36  1  0
 13 37  1  0
 13 38  1  0
 14 39  1  0
 16 40  1  0
 16 41  1  0
 17 42  1  0
 17 43  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
a-Bisabolol oxide b	Generator
Α-bisabolol oxide b	Generator
Bisabololoxide b	MeSH
(-)-alpha-Bisabolol oxide b	HMDB
(-)-Bisabolol oxide b	HMDB
Bisabolol oxide b	HMDB
Bisabolol oxide II	HMDB

Chemical Formula

C₁₅H₂₆O₂

Average Molecular Weight

238.3657

Monoisotopic Molecular Weight

238.193280076

IUPAC Name

2-[5-methyl-5-(4-methylcyclohex-3-en-1-yl)oxolan-2-yl]propan-2-ol

Traditional Name

2-[5-methyl-5-(4-methylcyclohex-3-en-1-yl)oxolan-2-yl]propan-2-ol

CAS Registry Number

26184-88-3

SMILES

CC1=CCC(CC1)C1(C)CCC(O1)C(C)(C)O

InChI Identifier

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

InChI Key

RKBAYVATPNYHLW-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tetrahydrofurans. These are heterocyclic compounds containing a saturated, aliphatic, five-membered ring where a carbon is replaced by an oxygen.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Tetrahydrofurans

Sub Class

Not Available

Direct Parent

Tetrahydrofurans

Alternative Parents

Substituents

Tetrahydrofuran
Tertiary alcohol
Oxacycle
Ether
Dialkyl ether
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Alcohol
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

oxolanes (CHEBI:80720 )

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cell membrane (HMDB: HMDB0038197)

Cellular substructure

Membrane (HMDB: HMDB0038197)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0038197)

Source

Exogenous

Food

Food (HMDB: HMDB0038197)

Tea

Herb and spice

Herb

Roman camomile (FooDB: FOOD00046)
German camomile (FooDB: FOOD00107)

Herbs and Spices (FooDB: FOOD00866)

Fat and oil

Fats and oils (FooDB: FOOD00864)

Endogenous

Plant

Plant (HMDB: HMDB0038197)

Not Available

Nutrient (HMDB: HMDB0038197)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0038197)

Emulsifier (HMDB: HMDB0038197)

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	0.14 g/L	ALOGPS
logP	3.56	ALOGPS
logP	2.93	ChemAxon
logS	-3.2	ALOGPS
pKa (Strongest Acidic)	14.33	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	29.46 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	71.02 m³·mol⁻¹	ChemAxon
Polarizability	28.85 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	157.41	31661259
DarkChem	[M-H]-	154.88	31661259
DeepCCS	[M+H]+	164.76	30932474
DeepCCS	[M-H]-	162.402	30932474
DeepCCS	[M-2H]-	195.288	30932474
DeepCCS	[M+Na]+	170.853	30932474
AllCCS	[M+H]+	158.8	32859911
AllCCS	[M+H-H2O]+	155.1	32859911
AllCCS	[M+NH4]+	162.3	32859911
AllCCS	[M+Na]+	163.4	32859911
AllCCS	[M-H]-	166.6	32859911
AllCCS	[M+Na-2H]-	167.3	32859911
AllCCS	[M+HCOO]-	168.2	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
alpha-Bisabolol oxide B	CC1=CCC(CC1)C1(C)CCC(O1)C(C)(C)O	2498.4	Standard polar	33892256
alpha-Bisabolol oxide B	CC1=CCC(CC1)C1(C)CCC(O1)C(C)(C)O	1642.7	Standard non polar	33892256
alpha-Bisabolol oxide B	CC1=CCC(CC1)C1(C)CCC(O1)C(C)(C)O	1642.6	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
alpha-Bisabolol oxide B,1TMS,isomer #1	CC1=CCC(C2(C)CCC(C(C)(C)O[Si](C)(C)C)O2)CC1	1809.6	Semi standard non polar	33892256
alpha-Bisabolol oxide B,1TBDMS,isomer #1	CC1=CCC(C2(C)CCC(C(C)(C)O[Si](C)(C)C(C)(C)C)O2)CC1	2046.5	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 - alpha-Bisabolol oxide B GC-MS (Non-derivatized) - 70eV, Positive	splash10-0a4i-9310000000-a7fd0f32874a6a85c656	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - alpha-Bisabolol oxide B GC-MS (1 TMS) - 70eV, Positive	splash10-001j-9840000000-774a13c3b6a9f2348b81	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - alpha-Bisabolol oxide B GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - alpha-Bisabolol oxide B 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 - alpha-Bisabolol oxide B 10V, Positive-QTOF	splash10-000i-1390000000-112c4ece87eb8afc0bd5	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - alpha-Bisabolol oxide B 20V, Positive-QTOF	splash10-0080-9750000000-1a037008e381a275741d	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - alpha-Bisabolol oxide B 40V, Positive-QTOF	splash10-0pb9-9500000000-9b22ad75939e4392d354	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - alpha-Bisabolol oxide B 10V, Negative-QTOF	splash10-000i-0190000000-5bbd104dc57a44a6ae90	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - alpha-Bisabolol oxide B 20V, Negative-QTOF	splash10-000i-1490000000-aaeb6ce808315d748691	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - alpha-Bisabolol oxide B 40V, Negative-QTOF	splash10-0uds-4910000000-09872c033cc368c100c7	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - alpha-Bisabolol oxide B 10V, Positive-QTOF	splash10-000i-1590000000-4ae32f9b1bb6d3128f57	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - alpha-Bisabolol oxide B 20V, Positive-QTOF	splash10-01bi-5920000000-b435a4101bd181e31862	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - alpha-Bisabolol oxide B 40V, Positive-QTOF	splash10-05ox-9000000000-84b1fef4ae8a7c7702be	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - alpha-Bisabolol oxide B 10V, Negative-QTOF	splash10-000i-0090000000-e665f494a7390ebf108d	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - alpha-Bisabolol oxide B 20V, Negative-QTOF	splash10-000i-0490000000-a286a4afcd3e92118fe8	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - alpha-Bisabolol oxide B 40V, Negative-QTOF	splash10-00y0-1920000000-8a873b56f3c9813be9dc	2021-09-23	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

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

KNApSAcK ID

Chemspider ID

KEGG Compound ID

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

117301

PDB ID

Not Available

ChEBI ID

80720

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

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

Showing metabocard for alpha-Bisabolol oxide B (HMDB0038197)

MOL for HMDB0038197 (alpha-Bisabolol oxide B)

3D MOL for HMDB0038197 (alpha-Bisabolol oxide B)

3D SDF for HMDB0038197 (alpha-Bisabolol oxide B)

3D-SDF for HMDB0038197 (alpha-Bisabolol oxide B)

PDB for HMDB0038197 (alpha-Bisabolol oxide B)

3D PDB for HMDB0038197 (alpha-Bisabolol oxide B)

SMILES for HMDB0038197 (alpha-Bisabolol oxide B)

INCHI for HMDB0038197 (alpha-Bisabolol oxide B)

Structure for HMDB0038197 (alpha-Bisabolol oxide B)

3D Structure for HMDB0038197 (alpha-Bisabolol oxide B)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra