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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 20:51:31 UTC

Update Date

2022-03-07 02:54:39 UTC

HMDB ID

HMDB0035835

Secondary Accession Numbers

HMDB35835

Metabolite Identification

Common Name

Furanoeremophilane

Description

Furanoeremophilane belongs to the class of organic compounds known as eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids. These are sesquiterpenoids with a structure based either on the eremophilane skeleton, its 8,9-seco derivative, or the furoeremophilane skeleton. Eremophilanes have been shown to be derived from eudesmanes by migration of the methyl group at C-10 to C-5. Based on a literature review a small amount of articles have been published on Furanoeremophilane.

Structure

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

HMDB0035835
     RDKit          3D
Furanoeremophilane
 38 40  0  0  0  0  0  0  0  0999 V2000
   -4.0439    1.2220   -0.4759 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3067   -0.0449   -0.4177 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8206   -1.3222   -0.3663 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8709   -2.2005   -0.3235 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7185   -1.5628   -0.3439 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9209   -0.2267   -0.4020 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8199    0.7630   -0.4377 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4593    0.1913    0.1071 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4069    0.2952    1.6095 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6405    1.0524   -0.3552 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4624    2.4899   -0.0567 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8927    0.5618    0.3384 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1398   -0.8999    0.0104 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9504   -1.7519    0.3040 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7360   -1.1813   -0.3942 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3628   -2.1532   -0.3110 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1083    1.6491   -1.4869 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6337    1.9263    0.2728 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1048    1.0287   -0.1555 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8945   -1.5643   -0.3623 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6728    1.1860   -1.4425 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1478    1.6010    0.2453 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2428   -0.1627    2.1273 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4017    1.3817    1.8566 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5427   -0.1506    1.9586 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8036    0.8647   -1.4492 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0026    2.8000    0.8813 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9832    3.0754   -0.8690 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4436    2.8557    0.0111 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9078    0.7723    1.4101 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7510    1.1222   -0.1136 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0268   -1.2291    0.5744 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3087   -0.9375   -1.0998 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1378   -2.7513   -0.1895 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7861   -1.9742    1.3631 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0364   -1.0812   -1.4793 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3063   -2.8747   -1.1557 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2446   -2.7696    0.6177 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  2  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
  6  2  1  0
 15  8  1  0
 16  5  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  3 20  1  0
  7 21  1  0
  7 22  1  0
  9 23  1  0
  9 24  1  0
  9 25  1  0
 10 26  1  0
 11 27  1  0
 11 28  1  0
 11 29  1  0
 12 30  1  0
 12 31  1  0
 13 32  1  0
 13 33  1  0
 14 34  1  0
 14 35  1  0
 15 36  1  0
 16 37  1  0
 16 38  1  0
M  END


  Mrv0541 05061308442D          

 16 18  0  0  0  0            999 V2000
    4.6119   -2.2771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8419   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3570   -1.4924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3570   -0.1576    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  5  4  1  0  0  0  0
  6  4  1  0  0  0  0
 10  1  1  0  0  0  0
 10  9  2  0  0  0  0
 11  2  1  0  0  0  0
 11  5  1  0  0  0  0
 12  6  1  0  0  0  0
 12  7  1  0  0  0  0
 13  8  1  0  0  0  0
 13 10  1  0  0  0  0
 14  7  1  0  0  0  0
 14 13  2  0  0  0  0
 15  3  1  0  0  0  0
 15  8  1  0  0  0  0
 15 11  1  0  0  0  0
 15 12  1  0  0  0  0
 16  9  1  0  0  0  0
 16 14  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0035835

> <DATABASE_NAME>
hmdb

> <SMILES>
CC1CCCC2CC3=C(CC12C)C(C)=CO3

> <INCHI_IDENTIFIER>
InChI=1S/C15H22O/c1-10-9-16-14-7-12-6-4-5-11(2)15(12,3)8-13(10)14/h9,11-12H,4-8H2,1-3H3

> <INCHI_KEY>
LCYZOSVRKHROOX-UHFFFAOYSA-N

> <FORMULA>
C15H22O

> <MOLECULAR_WEIGHT>
218.3346

> <EXACT_MASS>
218.167065326

> <JCHEM_ACCEPTOR_COUNT>
0

> <JCHEM_AVERAGE_POLARIZABILITY>
26.629177285396796

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3,4a,5-trimethyl-4H,4aH,5H,6H,7H,8H,8aH,9H-naphtho[2,3-b]furan

> <ALOGPS_LOGP>
5.23

> <JCHEM_LOGP>
4.429776431666667

> <ALOGPS_LOGS>
-4.43

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-1.476503220342451

> <JCHEM_POLAR_SURFACE_AREA>
13.14

> <JCHEM_REFRACTIVITY>
66.647

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.18e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3,4a,5-trimethyl-4H,5H,6H,7H,8H,8aH,9H-naphtho[2,3-b]furan

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0035835
     RDKit          3D
Furanoeremophilane
 38 40  0  0  0  0  0  0  0  0999 V2000
   -4.0439    1.2220   -0.4759 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3067   -0.0449   -0.4177 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8206   -1.3222   -0.3663 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8709   -2.2005   -0.3235 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7185   -1.5628   -0.3439 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9209   -0.2267   -0.4020 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8199    0.7630   -0.4377 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4593    0.1913    0.1071 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4069    0.2952    1.6095 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6405    1.0524   -0.3552 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4624    2.4899   -0.0567 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8927    0.5618    0.3384 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1398   -0.8999    0.0104 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9504   -1.7519    0.3040 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7360   -1.1813   -0.3942 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3628   -2.1532   -0.3110 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1083    1.6491   -1.4869 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6337    1.9263    0.2728 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1048    1.0287   -0.1555 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8945   -1.5643   -0.3623 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6728    1.1860   -1.4425 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1478    1.6010    0.2453 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2428   -0.1627    2.1273 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4017    1.3817    1.8566 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5427   -0.1506    1.9586 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8036    0.8647   -1.4492 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0026    2.8000    0.8813 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9832    3.0754   -0.8690 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4436    2.8557    0.0111 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9078    0.7723    1.4101 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7510    1.1222   -0.1136 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0268   -1.2291    0.5744 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3087   -0.9375   -1.0998 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1378   -2.7513   -0.1895 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7861   -1.9742    1.3631 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0364   -1.0812   -1.4793 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3063   -2.8747   -1.1557 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2446   -2.7696    0.6177 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  2  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
  6  2  1  0
 15  8  1  0
 16  5  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  3 20  1  0
  7 21  1  0
  7 22  1  0
  9 23  1  0
  9 24  1  0
  9 25  1  0
 10 26  1  0
 11 27  1  0
 11 28  1  0
 11 29  1  0
 12 30  1  0
 12 31  1  0
 13 32  1  0
 13 33  1  0
 14 34  1  0
 14 35  1  0
 15 36  1  0
 16 37  1  0
 16 38  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       8.609  -4.251   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.001  -3.850   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.038  -1.540   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.133  -2.786   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       8.133  -0.294   0.000  0.00  0.00           O+0
CONECT    1   10                                                            
CONECT    2   11                                                            
CONECT    3   15                                                            
CONECT    4    5    6                                                       
CONECT    5    4   11                                                       
CONECT    6    4   12                                                       
CONECT    7   12   14                                                       
CONECT    8   13   15                                                       
CONECT    9   10   16                                                       
CONECT   10    1    9   13                                                  
CONECT   11    2    5   15                                                  
CONECT   12    6    7   15                                                  
CONECT   13    8   10   14                                                  
CONECT   14    7   13   16                                                  
CONECT   15    3    8   11   12                                             
CONECT   16    9   14                                                       
MASTER        0    0    0    0    0    0    0    0   16    0   36    0
END

COMPND    HMDB0035835
HETATM    1  C1  UNL     1      -4.044   1.222  -0.476  1.00  0.00           C  
HETATM    2  C2  UNL     1      -3.307  -0.045  -0.418  1.00  0.00           C  
HETATM    3  C3  UNL     1      -3.821  -1.322  -0.366  1.00  0.00           C  
HETATM    4  O1  UNL     1      -2.871  -2.201  -0.323  1.00  0.00           O  
HETATM    5  C4  UNL     1      -1.719  -1.563  -0.344  1.00  0.00           C  
HETATM    6  C5  UNL     1      -1.921  -0.227  -0.402  1.00  0.00           C  
HETATM    7  C6  UNL     1      -0.820   0.763  -0.438  1.00  0.00           C  
HETATM    8  C7  UNL     1       0.459   0.191   0.107  1.00  0.00           C  
HETATM    9  C8  UNL     1       0.407   0.295   1.609  1.00  0.00           C  
HETATM   10  C9  UNL     1       1.640   1.052  -0.355  1.00  0.00           C  
HETATM   11  C10 UNL     1       1.462   2.490  -0.057  1.00  0.00           C  
HETATM   12  C11 UNL     1       2.893   0.562   0.338  1.00  0.00           C  
HETATM   13  C12 UNL     1       3.140  -0.900   0.010  1.00  0.00           C  
HETATM   14  C13 UNL     1       1.950  -1.752   0.304  1.00  0.00           C  
HETATM   15  C14 UNL     1       0.736  -1.181  -0.394  1.00  0.00           C  
HETATM   16  C15 UNL     1      -0.363  -2.153  -0.311  1.00  0.00           C  
HETATM   17  H1  UNL     1      -4.108   1.649  -1.487  1.00  0.00           H  
HETATM   18  H2  UNL     1      -3.634   1.926   0.273  1.00  0.00           H  
HETATM   19  H3  UNL     1      -5.105   1.029  -0.155  1.00  0.00           H  
HETATM   20  H4  UNL     1      -4.895  -1.564  -0.362  1.00  0.00           H  
HETATM   21  H5  UNL     1      -0.673   1.186  -1.443  1.00  0.00           H  
HETATM   22  H6  UNL     1      -1.148   1.601   0.245  1.00  0.00           H  
HETATM   23  H7  UNL     1       1.243  -0.163   2.127  1.00  0.00           H  
HETATM   24  H8  UNL     1       0.402   1.382   1.857  1.00  0.00           H  
HETATM   25  H9  UNL     1      -0.543  -0.151   1.959  1.00  0.00           H  
HETATM   26  H10 UNL     1       1.804   0.865  -1.449  1.00  0.00           H  
HETATM   27  H11 UNL     1       2.003   2.800   0.881  1.00  0.00           H  
HETATM   28  H12 UNL     1       1.983   3.075  -0.869  1.00  0.00           H  
HETATM   29  H13 UNL     1       0.444   2.856   0.011  1.00  0.00           H  
HETATM   30  H14 UNL     1       2.908   0.772   1.410  1.00  0.00           H  
HETATM   31  H15 UNL     1       3.751   1.122  -0.114  1.00  0.00           H  
HETATM   32  H16 UNL     1       4.027  -1.229   0.574  1.00  0.00           H  
HETATM   33  H17 UNL     1       3.309  -0.937  -1.100  1.00  0.00           H  
HETATM   34  H18 UNL     1       2.138  -2.751  -0.190  1.00  0.00           H  
HETATM   35  H19 UNL     1       1.786  -1.974   1.363  1.00  0.00           H  
HETATM   36  H20 UNL     1       1.036  -1.081  -1.479  1.00  0.00           H  
HETATM   37  H21 UNL     1      -0.306  -2.875  -1.156  1.00  0.00           H  
HETATM   38  H22 UNL     1      -0.245  -2.770   0.618  1.00  0.00           H  
CONECT    1    2   17   18   19
CONECT    2    3    3    6
CONECT    3    4   20
CONECT    4    5
CONECT    5    6    6   16
CONECT    6    7
CONECT    7    8   21   22
CONECT    8    9   10   15
CONECT    9   23   24   25
CONECT   10   11   12   26
CONECT   11   27   28   29
CONECT   12   13   30   31
CONECT   13   14   32   33
CONECT   14   15   34   35
CONECT   15   16   36
CONECT   16   37   38
END

HMDB0035835
     RDKit          3D
Furanoeremophilane
 38 40  0  0  0  0  0  0  0  0999 V2000
   -4.0439    1.2220   -0.4759 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3067   -0.0449   -0.4177 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8206   -1.3222   -0.3663 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8709   -2.2005   -0.3235 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7185   -1.5628   -0.3439 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9209   -0.2267   -0.4020 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8199    0.7630   -0.4377 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4593    0.1913    0.1071 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4069    0.2952    1.6095 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6405    1.0524   -0.3552 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4624    2.4899   -0.0567 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8927    0.5618    0.3384 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1398   -0.8999    0.0104 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9504   -1.7519    0.3040 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7360   -1.1813   -0.3942 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3628   -2.1532   -0.3110 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1083    1.6491   -1.4869 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6337    1.9263    0.2728 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1048    1.0287   -0.1555 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8945   -1.5643   -0.3623 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6728    1.1860   -1.4425 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1478    1.6010    0.2453 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2428   -0.1627    2.1273 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4017    1.3817    1.8566 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5427   -0.1506    1.9586 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8036    0.8647   -1.4492 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0026    2.8000    0.8813 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9832    3.0754   -0.8690 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4436    2.8557    0.0111 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9078    0.7723    1.4101 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7510    1.1222   -0.1136 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0268   -1.2291    0.5744 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3087   -0.9375   -1.0998 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1378   -2.7513   -0.1895 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7861   -1.9742    1.3631 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0364   -1.0812   -1.4793 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3063   -2.8747   -1.1557 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2446   -2.7696    0.6177 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  2  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
  6  2  1  0
 15  8  1  0
 16  5  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  3 20  1  0
  7 21  1  0
  7 22  1  0
  9 23  1  0
  9 24  1  0
  9 25  1  0
 10 26  1  0
 11 27  1  0
 11 28  1  0
 11 29  1  0
 12 30  1  0
 12 31  1  0
 13 32  1  0
 13 33  1  0
 14 34  1  0
 14 35  1  0
 15 36  1  0
 16 37  1  0
 16 38  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
10beta-Hydroxy-6beta-isobutyrylfuranoeremophilane	HMDB
Furoeremophilane	HMDB
Furanoeremophilane	MeSH

Chemical Formula

C₁₅H₂₂O

Average Molecular Weight

218.3346

Monoisotopic Molecular Weight

218.167065326

IUPAC Name

3,4a,5-trimethyl-4H,4aH,5H,6H,7H,8H,8aH,9H-naphtho[2,3-b]furan

Traditional Name

3,4a,5-trimethyl-4H,5H,6H,7H,8H,8aH,9H-naphtho[2,3-b]furan

CAS Registry Number

6750-13-6

SMILES

CC1CCCC2CC3=C(CC12C)C(C)=CO3

InChI Identifier

InChI=1S/C15H22O/c1-10-9-16-14-7-12-6-4-5-11(2)15(12,3)8-13(10)14/h9,11-12H,4-8H2,1-3H3

InChI Key

LCYZOSVRKHROOX-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids. These are sesquiterpenoids with a structure based either on the eremophilane skeleton, its 8,9-seco derivative, or the furoeremophilane skeleton. Eremophilanes have been shown to be derived from eudesmanes by migration of the methyl group at C-10 to C-5.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids

Alternative Parents

Substituents

Furoeremophilane sesquiterpenoid
Naphthofuran
Benzofuran
Heteroaromatic compound
Furan
Oxacycle
Organoheterocyclic compound
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Route of exposure

Enteral

Ingestion (HMDB: HMDB0035835)

Source

Endogenous

Endogenous (HMDB: HMDB0035835)

Plant

Plant (HMDB: HMDB0035835)

Animal

Animal (HMDB: HMDB0035835)

Exogenous

Food

Food (HMDB: HMDB0035835)

Vegetable

Other vegetable

Giant butterbur (FooDB: FOOD00314)

Leaf vegetable

Green vegetables (FooDB: FOOD00872)

Exogenous (HMDB: HMDB0035835)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid Peroxidation (HMDB: HMDB0035835)

Biochemical pathway

Metabolic pathway

Fatty Acid Metabolism (HMDB: HMDB0035835)

Lipid metabolism pathway (HMDB: HMDB0035835)

Cellular process

Cell signaling (HMDB: HMDB0035835)

Biochemical process

Lipid transport (HMDB: HMDB0035835)

Role

Biological role

Energy source (HMDB: HMDB0035835)

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	0.42 mg/L @ 25 °C (est)	The Good Scents Company Information System
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.0082 g/L	ALOGPS
logP	5.23	ALOGPS
logP	4.43	ChemAxon
logS	-4.4	ALOGPS
pKa (Strongest Basic)	-1.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	0	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	13.14 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	66.65 m³·mol⁻¹	ChemAxon
Polarizability	26.63 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]+	148.277	31661259
DarkChem	[M-H]-	148.025	31661259
DeepCCS	[M-2H]-	186.52	30932474
DeepCCS	[M+Na]+	162.191	30932474
AllCCS	[M+H]+	151.0	32859911
AllCCS	[M+H-H2O]+	147.0	32859911
AllCCS	[M+NH4]+	154.7	32859911
AllCCS	[M+Na]+	155.8	32859911
AllCCS	[M-H]-	160.8	32859911
AllCCS	[M+Na-2H]-	160.9	32859911
AllCCS	[M+HCOO]-	161.2	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.	7.44 minutes	32390414
Predicted by Siyang on May 30, 2022	21.8251 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	1.97 minutes	32390414
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	2293.4 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	801.1 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	297.3 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	486.2 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	480.4 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	854.8 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	1021.7 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	190.3 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	1833.5 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	680.6 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	1964.7 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	659.1 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	553.3 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	634.2 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	667.8 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	7.9 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Furanoeremophilane	CC1CCCC2CC3=C(CC12C)C(C)=CO3	2111.2	Standard polar	33892256
Furanoeremophilane	CC1CCCC2CC3=C(CC12C)C(C)=CO3	1609.7	Standard non polar	33892256
Furanoeremophilane	CC1CCCC2CC3=C(CC12C)C(C)=CO3	1682.5	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 - Furanoeremophilane GC-MS (Non-derivatized) - 70eV, Positive	splash10-0ug0-1920000000-6e08159c236d036e95aa	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Furanoeremophilane GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Furanoeremophilane 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 - Furanoeremophilane 10V, Positive-QTOF	splash10-014i-0190000000-20c7ef9f2a4a7e0dba5e	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Furanoeremophilane 20V, Positive-QTOF	splash10-01b9-2930000000-a14f727b3a4feeb03184	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Furanoeremophilane 40V, Positive-QTOF	splash10-0ldl-9400000000-f7422236a5d440928b76	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Furanoeremophilane 10V, Negative-QTOF	splash10-014i-0090000000-3d23045fe2b18a38b065	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Furanoeremophilane 20V, Negative-QTOF	splash10-014i-0190000000-e9761367ec3d57036ace	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Furanoeremophilane 40V, Negative-QTOF	splash10-0fg9-1910000000-3d4f2a94df3938e86b4d	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Furanoeremophilane 10V, Negative-QTOF	splash10-014i-0090000000-868e2fb00a2cfbf6c529	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Furanoeremophilane 20V, Negative-QTOF	splash10-014i-0090000000-868e2fb00a2cfbf6c529	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Furanoeremophilane 40V, Negative-QTOF	splash10-014i-0290000000-3327fd2a9bcb1641803e	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Furanoeremophilane 10V, Positive-QTOF	splash10-014i-0090000000-9487839d316c51b2aabd	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Furanoeremophilane 20V, Positive-QTOF	splash10-01b9-3960000000-f64619b4552071d14a4a	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Furanoeremophilane 40V, Positive-QTOF	splash10-014i-9300000000-7cc4111cff462df96523	2021-09-24	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

5317426

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

rw1851961

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 Furanoeremophilane (HMDB0035835)

MOL for HMDB0035835 (Furanoeremophilane)

3D MOL for HMDB0035835 (Furanoeremophilane)

3D SDF for HMDB0035835 (Furanoeremophilane)

3D-SDF for HMDB0035835 (Furanoeremophilane)

PDB for HMDB0035835 (Furanoeremophilane)

3D PDB for HMDB0035835 (Furanoeremophilane)

SMILES for HMDB0035835 (Furanoeremophilane)

INCHI for HMDB0035835 (Furanoeremophilane)

Structure for HMDB0035835 (Furanoeremophilane)

3D Structure for HMDB0035835 (Furanoeremophilane)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

GC-MS Spectra

MS/MS Spectra