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Showing metabocard for (+)-Isoborneol (HMDB0035815)

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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-11 20:50:19 UTC
Update Date2023-02-21 17:24:55 UTC
HMDB IDHMDB0035815
Secondary Accession Numbers
  • HMDB35815
Metabolite Identification
Common Name(+)-Isoborneol
Description(+)-Isoborneol, also known as isobornyl alcohol, belongs to the class of organic compounds known as bicyclic monoterpenoids. These are monoterpenoids containing exactly 2 rings, which are fused to each other. Based on a literature review a small amount of articles have been published on (+)-Isoborneol.
Structure
Data?1677000295
MOL3D MOLSDF3D SDFPDB3D PDBSMILESInChI

MOL for HMDB0035815 ((+)-Isoborneol)


  Mrv1652303062020462D          

 11 12  0  0  1  0            999 V2000
    2.1600   -1.5380    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8742   -1.9509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8742   -2.7742    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1600   -3.1872    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4458   -2.7742    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4458   -1.9509    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3366   -2.7820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6250   -2.3613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3444   -1.9561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7471   -1.5146    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1678   -0.7121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  8  1  6  0  0  0
  1 11  1  0  0  0  0
  1  2  1  0  0  0  0
  1  6  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  8  1  6  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6 10  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
M  END
Download

3D MOL for HMDB0035815 ((+)-Isoborneol)

HMDB0035815
     RDKit          3D
(+)-Isoborneol
 29 30  0  0  0  0  0  0  0  0999 V2000
   -1.0670    0.0437   -1.7467 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1795    0.4871   -0.6272 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8609    1.4423   -1.0591 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9851    0.9684    0.5783 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8751   -0.2449    0.7602 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8816   -1.3845    0.5903 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3983   -0.7539    0.0708 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2115   -1.6042   -0.7912 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0793   -0.1308    1.2462 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2779    0.4687    0.9695 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0537    0.9303    1.6606 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4261   -0.9800   -1.6518 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9449    0.7183   -1.8411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4590    0.0836   -2.6877 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5501    1.8609   -2.0616 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9818    2.3363   -0.4100 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8555    0.9544   -1.2777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4935    1.8951    0.4323 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3683   -0.2443    1.7304 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5861   -0.2690   -0.0915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6736   -1.7697    1.6267 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2524   -2.1984   -0.0251 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0011   -2.7031   -0.7301 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0185   -1.3437   -1.8671 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3141   -1.4795   -0.6660 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2373   -0.8792    2.0388 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2809    1.3827    1.3690 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5171    1.8927    1.8824 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4460    0.5204    2.5786 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  6
  7  9  1  0
  9 10  1  0
  9 11  1  0
  7  2  1  0
 11  4  1  0
  1 12  1  0
  1 13  1  0
  1 14  1  0
  3 15  1  0
  3 16  1  0
  3 17  1  0
  4 18  1  6
  5 19  1  0
  5 20  1  0
  6 21  1  0
  6 22  1  0
  8 23  1  0
  8 24  1  0
  8 25  1  0
  9 26  1  1
 10 27  1  0
 11 28  1  0
 11 29  1  0
M  END
Download

3D SDF for HMDB0035815 ((+)-Isoborneol)


  Mrv1652303062020462D          

 11 12  0  0  1  0            999 V2000
    2.1600   -1.5380    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8742   -1.9509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8742   -2.7742    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1600   -3.1872    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4458   -2.7742    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4458   -1.9509    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3366   -2.7820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6250   -2.3613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3444   -1.9561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7471   -1.5146    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1678   -0.7121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  8  1  6  0  0  0
  1 11  1  0  0  0  0
  1  2  1  0  0  0  0
  1  6  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  8  1  6  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6 10  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0035815

> <DATABASE_NAME>
hmdb

> <SMILES>
CC1(C)[C@H]2CC[C@]1(C)[C@@H](O)C2

> <INCHI_IDENTIFIER>
InChI=1S/C10H18O/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7-8,11H,4-6H2,1-3H3/t7-,8-,10+/m0/s1

> <INCHI_KEY>
DTGKSKDOIYIVQL-OYNCUSHFSA-N

> <FORMULA>
C10H18O

> <MOLECULAR_WEIGHT>
154.253

> <EXACT_MASS>
154.1357652

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
29

> <JCHEM_AVERAGE_POLARIZABILITY>
18.447352999747377

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2S,4S)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol

> <ALOGPS_LOGP>
2.83

> <JCHEM_LOGP>
1.9894578843333337

> <ALOGPS_LOGS>
-2.28

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
19.60482336496175

> <JCHEM_PKA_STRONGEST_BASIC>
-0.7846502601657298

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
45.314299999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.05e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,4S)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol

> <JCHEM_VEBER_RULE>
1

$$$$
Download

3D-SDF for HMDB0035815 ((+)-Isoborneol)

HMDB0035815
     RDKit          3D
(+)-Isoborneol
 29 30  0  0  0  0  0  0  0  0999 V2000
   -1.0670    0.0437   -1.7467 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1795    0.4871   -0.6272 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8609    1.4423   -1.0591 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9851    0.9684    0.5783 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8751   -0.2449    0.7602 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8816   -1.3845    0.5903 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3983   -0.7539    0.0708 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2115   -1.6042   -0.7912 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0793   -0.1308    1.2462 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2779    0.4687    0.9695 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0537    0.9303    1.6606 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4261   -0.9800   -1.6518 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9449    0.7183   -1.8411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4590    0.0836   -2.6877 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5501    1.8609   -2.0616 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9818    2.3363   -0.4100 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8555    0.9544   -1.2777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4935    1.8951    0.4323 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3683   -0.2443    1.7304 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5861   -0.2690   -0.0915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6736   -1.7697    1.6267 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2524   -2.1984   -0.0251 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0011   -2.7031   -0.7301 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0185   -1.3437   -1.8671 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3141   -1.4795   -0.6660 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2373   -0.8792    2.0388 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2809    1.3827    1.3690 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5171    1.8927    1.8824 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4460    0.5204    2.5786 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  6
  7  9  1  0
  9 10  1  0
  9 11  1  0
  7  2  1  0
 11  4  1  0
  1 12  1  0
  1 13  1  0
  1 14  1  0
  3 15  1  0
  3 16  1  0
  3 17  1  0
  4 18  1  6
  5 19  1  0
  5 20  1  0
  6 21  1  0
  6 22  1  0
  8 23  1  0
  8 24  1  0
  8 25  1  0
  9 26  1  1
 10 27  1  0
 11 28  1  0
 11 29  1  0
M  END
Download

PDB for HMDB0035815 ((+)-Isoborneol)

HEADER    PROTEIN                                 06-MAR-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAR-20         0                                  
HETATM    1  C   UNK     0       4.032  -2.871   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.365  -3.642   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.365  -5.179   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.032  -5.949   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.699  -5.179   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.699  -3.642   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.228  -5.193   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.900  -4.408   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.243  -3.651   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       1.395  -2.827   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       4.047  -1.329   0.000  0.00  0.00           C+0
CONECT    1    8   11    2    6                                             
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    8    5                                                  
CONECT    5    4    6                                                       
CONECT    6    1    5   10                                                  
CONECT    7    8                                                            
CONECT    8    1    4    7    9                                             
CONECT    9    8                                                            
CONECT   10    6                                                            
CONECT   11    1                                                            
MASTER        0    0    0    0    0    0    0    0   11    0   24    0
END
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3D PDB for HMDB0035815 ((+)-Isoborneol)

COMPND    HMDB0035815
HETATM    1  C1  UNL     1      -1.067   0.044  -1.747  1.00  0.00           C  
HETATM    2  C2  UNL     1      -0.179   0.487  -0.627  1.00  0.00           C  
HETATM    3  C3  UNL     1       0.861   1.442  -1.059  1.00  0.00           C  
HETATM    4  C4  UNL     1      -0.985   0.968   0.578  1.00  0.00           C  
HETATM    5  C5  UNL     1      -1.875  -0.245   0.760  1.00  0.00           C  
HETATM    6  C6  UNL     1      -0.882  -1.385   0.590  1.00  0.00           C  
HETATM    7  C7  UNL     1       0.398  -0.754   0.071  1.00  0.00           C  
HETATM    8  C8  UNL     1       1.212  -1.604  -0.791  1.00  0.00           C  
HETATM    9  C9  UNL     1       1.079  -0.131   1.246  1.00  0.00           C  
HETATM   10  O1  UNL     1       2.278   0.469   0.969  1.00  0.00           O  
HETATM   11  C10 UNL     1       0.054   0.930   1.661  1.00  0.00           C  
HETATM   12  H1  UNL     1      -1.426  -0.980  -1.652  1.00  0.00           H  
HETATM   13  H2  UNL     1      -1.945   0.718  -1.841  1.00  0.00           H  
HETATM   14  H3  UNL     1      -0.459   0.084  -2.688  1.00  0.00           H  
HETATM   15  H4  UNL     1       0.550   1.861  -2.062  1.00  0.00           H  
HETATM   16  H5  UNL     1       0.982   2.336  -0.410  1.00  0.00           H  
HETATM   17  H6  UNL     1       1.855   0.954  -1.278  1.00  0.00           H  
HETATM   18  H7  UNL     1      -1.493   1.895   0.432  1.00  0.00           H  
HETATM   19  H8  UNL     1      -2.368  -0.244   1.730  1.00  0.00           H  
HETATM   20  H9  UNL     1      -2.586  -0.269  -0.092  1.00  0.00           H  
HETATM   21  H10 UNL     1      -0.674  -1.770   1.627  1.00  0.00           H  
HETATM   22  H11 UNL     1      -1.252  -2.198  -0.025  1.00  0.00           H  
HETATM   23  H12 UNL     1       1.001  -2.703  -0.730  1.00  0.00           H  
HETATM   24  H13 UNL     1       1.018  -1.344  -1.867  1.00  0.00           H  
HETATM   25  H14 UNL     1       2.314  -1.480  -0.666  1.00  0.00           H  
HETATM   26  H15 UNL     1       1.237  -0.879   2.039  1.00  0.00           H  
HETATM   27  H16 UNL     1       2.281   1.383   1.369  1.00  0.00           H  
HETATM   28  H17 UNL     1       0.517   1.893   1.882  1.00  0.00           H  
HETATM   29  H18 UNL     1      -0.446   0.520   2.579  1.00  0.00           H  
CONECT    1    2   12   13   14
CONECT    2    3    4    7
CONECT    3   15   16   17
CONECT    4    5   11   18
CONECT    5    6   19   20
CONECT    6    7   21   22
CONECT    7    8    9
CONECT    8   23   24   25
CONECT    9   10   11   26
CONECT   10   27
CONECT   11   28   29
END
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SMILES for HMDB0035815 ((+)-Isoborneol)

CC1(C)[C@H]2CC[C@]1(C)[C@@H](O)C2
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INCHI for HMDB0035815 ((+)-Isoborneol)

InChI=1S/C10H18O/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7-8,11H,4-6H2,1-3H3/t7-,8-,10+/m0/s1
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View in JSmolView Stereo Labels
Synonyms
ValueSource
(1S,2S,4S)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-olHMDB
(S,S,S)-(+)-IsoborneolHMDB
2-exo-Bornyl alcoholHMDB
IsoborneolHMDB
Isobornyl alcoholHMDB
exo-2-Hydroxy-1,7,7-trimethylnorbornaneHMDB
(+)-IsoborneolHMDB
Chemical FormulaC10H18O
Average Molecular Weight154.253
Monoisotopic Molecular Weight154.1357652
IUPAC Name(1S,2S,4S)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol
Traditional Name(1S,2S,4S)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol
CAS Registry Number16725-71-6
SMILES
CC1(C)[C@H]2CC[C@]1(C)[C@@H](O)C2
InChI Identifier
InChI=1S/C10H18O/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7-8,11H,4-6H2,1-3H3/t7-,8-,10+/m0/s1
InChI KeyDTGKSKDOIYIVQL-OYNCUSHFSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as bicyclic monoterpenoids. These are monoterpenoids containing exactly 2 rings, which are fused to each other.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassPrenol lipids
Sub ClassMonoterpenoids
Direct ParentBicyclic monoterpenoids
Alternative Parents
Substituents
  • Bicyclic monoterpenoid
  • Bornane monoterpenoid
  • Cyclic alcohol
  • Secondary alcohol
  • Organic oxygen compound
  • Hydrocarbon derivative
  • Organooxygen compound
  • Alcohol
  • Aliphatic homopolycyclic compound
Molecular FrameworkAliphatic homopolycyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
Biological location
ProcessNot Available
RoleNot Available
Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting Point214 °CNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility0.8 g/LALOGPS
logP2.83ALOGPS
logP1.99ChemAxon
logS-2.3ALOGPS
pKa (Strongest Acidic)19.6ChemAxon
pKa (Strongest Basic)-0.78ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count1ChemAxon
Hydrogen Donor Count1ChemAxon
Polar Surface Area20.23 ŲChemAxon
Rotatable Bond Count0ChemAxon
Refractivity45.31 m³·mol⁻¹ChemAxon
Polarizability18.45 ųChemAxon
Number of Rings2ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DeepCCS[M+H]+142.58830932474
DeepCCS[M-H]-140.19230932474
DeepCCS[M-2H]-173.89330932474
DeepCCS[M+Na]+148.530932474
AllCCS[M+H]+134.432859911
AllCCS[M+H-H2O]+130.132859911
AllCCS[M+NH4]+138.432859911
AllCCS[M+Na]+139.532859911
AllCCS[M-H]-136.832859911
AllCCS[M+Na-2H]-138.132859911
AllCCS[M+HCOO]-139.632859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
(+)-IsoborneolCC1(C)[C@H]2CC[C@]1(C)[C@@H](O)C21662.7Standard polar33892256
(+)-IsoborneolCC1(C)[C@H]2CC[C@]1(C)[C@@H](O)C21168.0Standard non polar33892256
(+)-IsoborneolCC1(C)[C@H]2CC[C@]1(C)[C@@H](O)C21153.7Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
(+)-Isoborneol,1TMS,isomer #1CC1(C)[C@H]2CC[C@]1(C)[C@@H](O[Si](C)(C)C)C21217.1Semi standard non polar33892256
(+)-Isoborneol,1TBDMS,isomer #1CC1(C)[C@H]2CC[C@]1(C)[C@@H](O[Si](C)(C)C(C)(C)C)C21477.0Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - (+)-Isoborneol GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (+)-Isoborneol 10V, Positive-QTOFsplash10-052r-0900000000-7eaa92cdc2cb1dd17c332016-06-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (+)-Isoborneol 20V, Positive-QTOFsplash10-052r-0900000000-fb1222abb6cef74eb0832016-06-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (+)-Isoborneol 40V, Positive-QTOFsplash10-00dr-2900000000-622438b8bd224a755c472016-06-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (+)-Isoborneol 10V, Negative-QTOFsplash10-0udi-0900000000-b64fc5b28acf2b8ce6ee2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (+)-Isoborneol 20V, Negative-QTOFsplash10-0udi-0900000000-404830ee9ef93bfec2b82016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (+)-Isoborneol 40V, Negative-QTOFsplash10-0fki-2900000000-5d8542e9c4643c74fa542016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (+)-Isoborneol 10V, Positive-QTOFsplash10-08fr-4900000000-c5fb0f5b567a4f9fada92021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (+)-Isoborneol 20V, Positive-QTOFsplash10-090r-9400000000-3329d0b3e6f71527a4bc2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (+)-Isoborneol 40V, Positive-QTOFsplash10-0006-9000000000-1ab95ec8cd37ae806b102021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (+)-Isoborneol 10V, Negative-QTOFsplash10-0udi-0900000000-d2363ae8d4dbdcccda802021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (+)-Isoborneol 20V, Negative-QTOFsplash10-0udi-0900000000-d2363ae8d4dbdcccda802021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (+)-Isoborneol 40V, Negative-QTOFsplash10-0udi-0900000000-4f86d6496a0b85050d5c2021-09-25Wishart LabView Spectrum

IR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted IR SpectrumIR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M-H]-)2023-02-04FELIX labView Spectrum
Predicted IR SpectrumIR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M+H]+)2023-02-04FELIX labView Spectrum
Predicted IR SpectrumIR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M+Na]+)2023-02-04FELIX labView Spectrum
Biological Properties
Cellular Locations
  • Extracellular
  • Membrane
Biospecimen LocationsNot Available
Tissue LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB014576
KNApSAcK IDNot Available
Chemspider ID16739225
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound6973640
PDB IDNot Available
ChEBI IDNot Available
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General References
  1. Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. [PubMed:11413487 ]
  2. 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 ]
  3. 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 ]
  4. 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 ]
  5. (). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .
  6. Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.