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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 22:38:22 UTC

Update Date

2022-03-07 02:55:18 UTC

HMDB ID

HMDB0037394

Secondary Accession Numbers

HMDB37394

Metabolite Identification

Common Name

3xi-4-Copanol

Description

3xi-4-Copanol 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 3xi-4-Copanol.

Structure

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

HMDB0037394
     RDKit          3D
3xi-4-Copanol
 42 44  0  0  0  0  0  0  0  0999 V2000
    3.9125   -0.2709   -0.3044 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6547   -0.4964    0.5461 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5057   -1.9778    0.7112 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4999   -0.0014   -0.2994 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6200    1.4502   -0.6574 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3235    2.1863   -0.6687 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8373    1.4192   -0.1414 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1017    2.1892   -0.1032 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4119    0.7472    1.1500 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6435    0.2419    1.8651 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6318   -0.4084    0.9685 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1574   -0.6949   -0.4099 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8362   -2.1907   -0.5281 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1082   -0.4356   -1.3994 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8915    0.0372   -0.7435 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1726   -0.3469    0.2963 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0616    0.8178   -0.3902 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6455   -0.6802   -1.3221 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7717   -0.8254    0.0722 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7424    0.0496    1.5054 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0505   -2.3956   -0.2197 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4905   -2.4333    0.8324 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8295   -2.2545    1.5623 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5754   -0.5732   -1.2710 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0819    1.5860   -1.6794 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3777    1.8984    0.0434 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0761    2.6241   -1.6704 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4531    3.0892   -0.0026 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9084    3.2418   -0.4651 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4807    2.3393    0.9481 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9024    1.8083   -0.7753 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2605    1.3002    1.7925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1182    1.0449    2.4934 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2753   -0.5112    2.6146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5762    0.2053    0.8788 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9923   -1.3728    1.4341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7099   -2.7650   -0.8753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5201   -2.6068    0.4478 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0019   -2.3367   -1.2452 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5749   -1.2586   -1.6787 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5326   -0.0792   -1.7602 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1072   -1.3607    0.6728 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 12 15  1  0
 15 16  1  0
 16  4  1  0
 15  7  1  0
 16  9  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
  3 23  1  0
  4 24  1  0
  5 25  1  0
  5 26  1  0
  6 27  1  0
  6 28  1  0
  8 29  1  0
  8 30  1  0
  8 31  1  0
  9 32  1  0
 10 33  1  0
 10 34  1  0
 11 35  1  0
 11 36  1  0
 13 37  1  0
 13 38  1  0
 13 39  1  0
 14 40  1  0
 15 41  1  0
 16 42  1  0
M  END

  Mrv0541 05061309462D          

 16 18  0  0  0  0            999 V2000
   -1.2256    1.1767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7434    1.8409    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0395    1.5807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5492   -0.9127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6814   -0.1452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9550    0.5634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5321    1.2790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3831    1.1289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7986    0.4479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1485   -0.0857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3679    0.6160    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0458    1.0449    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4254    0.5603    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0035    1.2149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3594    1.9076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4321   -0.3525    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  9  1  0  0  0  0
  1 14  1  0  0  0  0
  2  3  1  0  0  0  0
  3 11  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5 10  1  0  0  0  0
  5 16  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 11  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
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0037394

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(C)C1CCC2(C)C3CCC(C)(O)C2C13

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

> <INCHI_KEY>
AZCJPMYIWXNBMH-UHFFFAOYSA-N

> <FORMULA>
C15H26O

> <MOLECULAR_WEIGHT>
222.3663

> <EXACT_MASS>
222.198365454

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_AVERAGE_POLARIZABILITY>
27.440663685764868

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1,3-dimethyl-8-(propan-2-yl)tricyclo[4.4.0.0²,⁷]decan-3-ol

> <ALOGPS_LOGP>
2.80

> <JCHEM_LOGP>
3.1785024189999995

> <ALOGPS_LOGS>
-4.77

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-0.5672432191093345

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
66.6

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.82e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
8-isopropyl-1,3-dimethyltricyclo[4.4.0.0²,⁷]decan-3-ol

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0037394
     RDKit          3D
3xi-4-Copanol
 42 44  0  0  0  0  0  0  0  0999 V2000
    3.9125   -0.2709   -0.3044 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6547   -0.4964    0.5461 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5057   -1.9778    0.7112 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4999   -0.0014   -0.2994 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6200    1.4502   -0.6574 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3235    2.1863   -0.6687 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8373    1.4192   -0.1414 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1017    2.1892   -0.1032 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4119    0.7472    1.1500 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6435    0.2419    1.8651 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6318   -0.4084    0.9685 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1574   -0.6949   -0.4099 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8362   -2.1907   -0.5281 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1082   -0.4356   -1.3994 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8915    0.0372   -0.7435 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1726   -0.3469    0.2963 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0616    0.8178   -0.3902 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6455   -0.6802   -1.3221 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7717   -0.8254    0.0722 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7424    0.0496    1.5054 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0505   -2.3956   -0.2197 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4905   -2.4333    0.8324 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8295   -2.2545    1.5623 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5754   -0.5732   -1.2710 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0819    1.5860   -1.6794 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3777    1.8984    0.0434 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0761    2.6241   -1.6704 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4531    3.0892   -0.0026 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9084    3.2418   -0.4651 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4807    2.3393    0.9481 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9024    1.8083   -0.7753 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2605    1.3002    1.7925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1182    1.0449    2.4934 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2753   -0.5112    2.6146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5762    0.2053    0.8788 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9923   -1.3728    1.4341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7099   -2.7650   -0.8753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5201   -2.6068    0.4478 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0019   -2.3367   -1.2452 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5749   -1.2586   -1.6787 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5326   -0.0792   -1.7602 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1072   -1.3607    0.6728 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 12 15  1  0
 15 16  1  0
 16  4  1  0
 15  7  1  0
 16  9  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
  3 23  1  0
  4 24  1  0
  5 25  1  0
  5 26  1  0
  6 27  1  0
  6 28  1  0
  8 29  1  0
  8 30  1  0
  8 31  1  0
  9 32  1  0
 10 33  1  0
 10 34  1  0
 11 35  1  0
 11 36  1  0
 13 37  1  0
 13 38  1  0
 13 39  1  0
 14 40  1  0
 15 41  1  0
 16 42  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      -2.288   2.197   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.388   3.436   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.074   2.951   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.025  -1.704   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.272  -0.271   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.783   1.052   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.993   2.388   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.715   2.107   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.491   0.836   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.277  -0.160   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.687   1.150   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.952   1.951   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -4.527   1.046   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -3.740   2.268   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -4.404   3.561   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       2.673  -0.658   0.000  0.00  0.00           O+0
CONECT    1    2    9   14                                                  
CONECT    2    1    3                                                       
CONECT    3    2   11                                                       
CONECT    4    5                                                            
CONECT    5    4    6   10   16                                             
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   11                                                  
CONECT    9    1    8   10                                                  
CONECT   10    5    9   11                                                  
CONECT   11    3    8   10   12                                             
CONECT   12   11                                                            
CONECT   13   14                                                            
CONECT   14    1   13   15                                                  
CONECT   15   14                                                            
CONECT   16    5                                                            
MASTER        0    0    0    0    0    0    0    0   16    0   36    0
END

COMPND    HMDB0037394
HETATM    1  C1  UNL     1       3.912  -0.271  -0.304  1.00  0.00           C  
HETATM    2  C2  UNL     1       2.655  -0.496   0.546  1.00  0.00           C  
HETATM    3  C3  UNL     1       2.506  -1.978   0.711  1.00  0.00           C  
HETATM    4  C4  UNL     1       1.500  -0.001  -0.299  1.00  0.00           C  
HETATM    5  C5  UNL     1       1.620   1.450  -0.657  1.00  0.00           C  
HETATM    6  C6  UNL     1       0.324   2.186  -0.669  1.00  0.00           C  
HETATM    7  C7  UNL     1      -0.837   1.419  -0.141  1.00  0.00           C  
HETATM    8  C8  UNL     1      -2.102   2.189  -0.103  1.00  0.00           C  
HETATM    9  C9  UNL     1      -0.412   0.747   1.150  1.00  0.00           C  
HETATM   10  C10 UNL     1      -1.643   0.242   1.865  1.00  0.00           C  
HETATM   11  C11 UNL     1      -2.632  -0.408   0.968  1.00  0.00           C  
HETATM   12  C12 UNL     1      -2.157  -0.695  -0.410  1.00  0.00           C  
HETATM   13  C13 UNL     1      -1.836  -2.191  -0.528  1.00  0.00           C  
HETATM   14  O1  UNL     1      -3.108  -0.436  -1.399  1.00  0.00           O  
HETATM   15  C14 UNL     1      -0.892   0.037  -0.744  1.00  0.00           C  
HETATM   16  C15 UNL     1       0.173  -0.347   0.296  1.00  0.00           C  
HETATM   17  H1  UNL     1       4.062   0.818  -0.390  1.00  0.00           H  
HETATM   18  H2  UNL     1       3.646  -0.680  -1.322  1.00  0.00           H  
HETATM   19  H3  UNL     1       4.772  -0.825   0.072  1.00  0.00           H  
HETATM   20  H4  UNL     1       2.742   0.050   1.505  1.00  0.00           H  
HETATM   21  H5  UNL     1       2.051  -2.396  -0.220  1.00  0.00           H  
HETATM   22  H6  UNL     1       3.491  -2.433   0.832  1.00  0.00           H  
HETATM   23  H7  UNL     1       1.829  -2.254   1.562  1.00  0.00           H  
HETATM   24  H8  UNL     1       1.575  -0.573  -1.271  1.00  0.00           H  
HETATM   25  H9  UNL     1       2.082   1.586  -1.679  1.00  0.00           H  
HETATM   26  H10 UNL     1       2.378   1.898   0.043  1.00  0.00           H  
HETATM   27  H11 UNL     1       0.076   2.624  -1.670  1.00  0.00           H  
HETATM   28  H12 UNL     1       0.453   3.089  -0.003  1.00  0.00           H  
HETATM   29  H13 UNL     1      -1.908   3.242  -0.465  1.00  0.00           H  
HETATM   30  H14 UNL     1      -2.481   2.339   0.948  1.00  0.00           H  
HETATM   31  H15 UNL     1      -2.902   1.808  -0.775  1.00  0.00           H  
HETATM   32  H16 UNL     1       0.261   1.300   1.793  1.00  0.00           H  
HETATM   33  H17 UNL     1      -2.118   1.045   2.493  1.00  0.00           H  
HETATM   34  H18 UNL     1      -1.275  -0.511   2.615  1.00  0.00           H  
HETATM   35  H19 UNL     1      -3.576   0.205   0.879  1.00  0.00           H  
HETATM   36  H20 UNL     1      -2.992  -1.373   1.434  1.00  0.00           H  
HETATM   37  H21 UNL     1      -2.710  -2.765  -0.875  1.00  0.00           H  
HETATM   38  H22 UNL     1      -1.520  -2.607   0.448  1.00  0.00           H  
HETATM   39  H23 UNL     1      -1.002  -2.337  -1.245  1.00  0.00           H  
HETATM   40  H24 UNL     1      -3.575  -1.259  -1.679  1.00  0.00           H  
HETATM   41  H25 UNL     1      -0.533  -0.079  -1.760  1.00  0.00           H  
HETATM   42  H26 UNL     1       0.107  -1.361   0.673  1.00  0.00           H  
CONECT    1    2   17   18   19
CONECT    2    3    4   20
CONECT    3   21   22   23
CONECT    4    5   16   24
CONECT    5    6   25   26
CONECT    6    7   27   28
CONECT    7    8    9   15
CONECT    8   29   30   31
CONECT    9   10   16   32
CONECT   10   11   33   34
CONECT   11   12   35   36
CONECT   12   13   14   15
CONECT   13   37   38   39
CONECT   14   40
CONECT   15   16   41
CONECT   16   42
END

HMDB0037394
     RDKit          3D
3xi-4-Copanol
 42 44  0  0  0  0  0  0  0  0999 V2000
    3.9125   -0.2709   -0.3044 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6547   -0.4964    0.5461 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5057   -1.9778    0.7112 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4999   -0.0014   -0.2994 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6200    1.4502   -0.6574 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3235    2.1863   -0.6687 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8373    1.4192   -0.1414 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1017    2.1892   -0.1032 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4119    0.7472    1.1500 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6435    0.2419    1.8651 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6318   -0.4084    0.9685 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1574   -0.6949   -0.4099 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8362   -2.1907   -0.5281 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1082   -0.4356   -1.3994 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8915    0.0372   -0.7435 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1726   -0.3469    0.2963 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0616    0.8178   -0.3902 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6455   -0.6802   -1.3221 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7717   -0.8254    0.0722 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7424    0.0496    1.5054 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0505   -2.3956   -0.2197 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4905   -2.4333    0.8324 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8295   -2.2545    1.5623 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5754   -0.5732   -1.2710 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0819    1.5860   -1.6794 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3777    1.8984    0.0434 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0761    2.6241   -1.6704 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4531    3.0892   -0.0026 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9084    3.2418   -0.4651 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4807    2.3393    0.9481 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9024    1.8083   -0.7753 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2605    1.3002    1.7925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1182    1.0449    2.4934 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2753   -0.5112    2.6146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5762    0.2053    0.8788 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9923   -1.3728    1.4341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7099   -2.7650   -0.8753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5201   -2.6068    0.4478 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0019   -2.3367   -1.2452 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5749   -1.2586   -1.6787 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5326   -0.0792   -1.7602 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1072   -1.3607    0.6728 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 12 15  1  0
 15 16  1  0
 16  4  1  0
 15  7  1  0
 16  9  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
  3 23  1  0
  4 24  1  0
  5 25  1  0
  5 26  1  0
  6 27  1  0
  6 28  1  0
  8 29  1  0
  8 30  1  0
  8 31  1  0
  9 32  1  0
 10 33  1  0
 10 34  1  0
 11 35  1  0
 11 36  1  0
 13 37  1  0
 13 38  1  0
 13 39  1  0
 14 40  1  0
 15 41  1  0
 16 42  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
1-(4-Hydroxyphenyl)-1-nonanone	HMDB

Chemical Formula

C₁₅H₂₆O

Average Molecular Weight

222.3663

Monoisotopic Molecular Weight

222.198365454

IUPAC Name

1,3-dimethyl-8-(propan-2-yl)tricyclo[4.4.0.0²,⁷]decan-3-ol

Traditional Name

8-isopropyl-1,3-dimethyltricyclo[4.4.0.0²,⁷]decan-3-ol

CAS Registry Number

Not Available

SMILES

CC(C)C1CCC2(C)C3CCC(C)(O)C2C13

InChI Identifier

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

InChI Key

AZCJPMYIWXNBMH-UHFFFAOYSA-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

Copaane sesquiterpenoid
Sesquiterpenoid
Tertiary alcohol
Cyclic alcohol
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Route of exposure

Enteral

Ingestion (HMDB: HMDB0037394)

Source

Endogenous

Endogenous (HMDB: HMDB0037394)

Plant

Plant (HMDB: HMDB0037394)

Animal

Animal (HMDB: HMDB0037394)

Exogenous

Food

Food (HMDB: HMDB0037394)

Herb and spice

Herbs and Spices (FooDB: FOOD00866)

Exogenous (HMDB: HMDB0037394)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid Peroxidation (HMDB: HMDB0037394)

Biochemical pathway

Metabolic pathway

Fatty Acid Metabolism (HMDB: HMDB0037394)

Lipid metabolism pathway (HMDB: HMDB0037394)

Cellular process

Cell signaling (HMDB: HMDB0037394)

Biochemical process

Lipid transport (HMDB: HMDB0037394)

Role

Biological role

Energy source (HMDB: HMDB0037394)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0037394)

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	102 °C	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	0.0038 g/L	ALOGPS
logP	2.8	ALOGPS
logP	3.18	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Basic)	-0.57	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	1	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]+	152.139	31661259
DarkChem	[M-H]-	146.893	31661259
DeepCCS	[M-2H]-	192.181	30932474
DeepCCS	[M+Na]+	168.235	30932474
AllCCS	[M+H]+	152.2	32859911
AllCCS	[M+H-H2O]+	148.5	32859911
AllCCS	[M+NH4]+	155.6	32859911
AllCCS	[M+Na]+	156.6	32859911
AllCCS	[M-H]-	161.9	32859911
AllCCS	[M+Na-2H]-	162.3	32859911
AllCCS	[M+HCOO]-	162.8	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
3xi-4-Copanol	CC(C)C1CCC2(C)C3CCC(C)(O)C2C13	2068.2	Standard polar	33892256
3xi-4-Copanol	CC(C)C1CCC2(C)C3CCC(C)(O)C2C13	1579.6	Standard non polar	33892256
3xi-4-Copanol	CC(C)C1CCC2(C)C3CCC(C)(O)C2C13	1529.4	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
3xi-4-Copanol,1TMS,isomer #1	CC(C)C1CCC2(C)C3CCC(C)(O[Si](C)(C)C)C2C13	1756.0	Semi standard non polar	33892256
3xi-4-Copanol,1TBDMS,isomer #1	CC(C)C1CCC2(C)C3CCC(C)(O[Si](C)(C)C(C)(C)C)C2C13	2018.7	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 - 3xi-4-Copanol GC-MS (Non-derivatized) - 70eV, Positive	splash10-0a4l-5940000000-903a84492616bc0c9323	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3xi-4-Copanol GC-MS (1 TMS) - 70eV, Positive	splash10-004i-9470000000-5c6f2446cab5f05ac722	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3xi-4-Copanol 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 - 3xi-4-Copanol 10V, Positive-QTOF	splash10-0ab9-0090000000-7657cebea381d3b87a4b	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3xi-4-Copanol 20V, Positive-QTOF	splash10-0ab9-0290000000-d0bb82a620f8cb1760f6	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3xi-4-Copanol 40V, Positive-QTOF	splash10-052r-0940000000-c5f37377b6d2d2db8319	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3xi-4-Copanol 10V, Negative-QTOF	splash10-00di-0090000000-ff47dd2aa7b3e29acf91	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3xi-4-Copanol 20V, Negative-QTOF	splash10-00di-0090000000-bdd340b7d9e6aeb6c301	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3xi-4-Copanol 40V, Negative-QTOF	splash10-0abi-0490000000-873717eccb4066c84cf6	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3xi-4-Copanol 10V, Negative-QTOF	splash10-00di-0090000000-ab61d8a2af41e6ed2e49	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3xi-4-Copanol 20V, Negative-QTOF	splash10-00di-0090000000-ab61d8a2af41e6ed2e49	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3xi-4-Copanol 40V, Negative-QTOF	splash10-00di-0090000000-ab61d8a2af41e6ed2e49	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3xi-4-Copanol 10V, Positive-QTOF	splash10-00di-0390000000-e999045823bc4abbcff0	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3xi-4-Copanol 20V, Positive-QTOF	splash10-0a4i-0190000000-785758f4f84ee6bfdcff	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3xi-4-Copanol 40V, Positive-QTOF	splash10-01vp-4930000000-2a0988234a9efe1fafba	2021-09-25	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

FDB016437

KNApSAcK ID

Not Available

Chemspider ID

146197

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

14807649

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. [PubMed:11413487 ]
Watson AD: Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Lipidomics: a global approach to lipid analysis in biological systems. J Lipid Res. 2006 Oct;47(10):2101-11. Epub 2006 Aug 10. [PubMed:16902246 ]
Sethi JK, Vidal-Puig AJ: Thematic review series: adipocyte biology. Adipose tissue function and plasticity orchestrate nutritional adaptation. J Lipid Res. 2007 Jun;48(6):1253-62. Epub 2007 Mar 20. [PubMed:17374880 ]
Lingwood D, Simons K: Lipid rafts as a membrane-organizing principle. Science. 2010 Jan 1;327(5961):46-50. doi: 10.1126/science.1174621. [PubMed:20044567 ]
(). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .
Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.

Showing metabocard for 3xi-4-Copanol (HMDB0037394)

MOL for HMDB0037394 (3xi-4-Copanol)

3D MOL for HMDB0037394 (3xi-4-Copanol)

3D SDF for HMDB0037394 (3xi-4-Copanol)

3D-SDF for HMDB0037394 (3xi-4-Copanol)

PDB for HMDB0037394 (3xi-4-Copanol)

3D PDB for HMDB0037394 (3xi-4-Copanol)

SMILES for HMDB0037394 (3xi-4-Copanol)

INCHI for HMDB0037394 (3xi-4-Copanol)

Structure for HMDB0037394 (3xi-4-Copanol)

3D Structure for HMDB0037394 (3xi-4-Copanol)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra