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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 20:43:48 UTC

Update Date

2022-03-07 02:54:36 UTC

HMDB ID

HMDB0035715

Secondary Accession Numbers

HMDB35715

Metabolite Identification

Common Name

Tanacetin

Description

Tanacetin belongs to the class of organic compounds known as eudesmanolides, secoeudesmanolides, and derivatives. These are terpenoids with a structure based on the eudesmanolide (a 3,5a,9-trimethyl-naphtho[1,2-b]furan-2-one derivative) or secoeudesmanolide (a 3,6-dimethyl-5-(pentan-2-yl)-1-benzofuran-2-one derivative) skeleton. Based on a literature review a small amount of articles have been published on Tanacetin.

Structure

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

HMDB0035715
     RDKit          3D
Tanacetin
 39 41  0  0  0  0  0  0  0  0999 V2000
    4.4243   -0.6399    0.1832 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1801   -0.3105   -0.0977 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7967    0.5018   -1.2459 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5499    0.9402   -2.1624 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4036    0.7267   -1.1660 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1136    0.6434    0.2148 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9007   -0.6230    0.5862 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3047   -1.8417   -0.0796 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0081   -1.5496   -0.7781 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9424   -0.7597    0.1216 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2250   -1.6691    1.3114 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2006   -0.5130   -0.6816 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8166    0.1587   -1.8438 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1097    0.4393    0.0934 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5350    1.8103   -0.0582 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0348    1.7325    0.0168 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3754    2.7962   -0.4295 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3269    0.5521    0.5533 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4184    0.5863    1.9549 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6789   -1.2559    1.0601 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2675   -0.3394   -0.4087 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5911    1.4544    0.8115 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0111   -0.7346    1.6670 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9836   -2.3009   -0.8264 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0743   -2.5693    0.7503 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1073   -1.1194   -1.7743 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5030   -2.5470   -0.9205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3580   -1.5605    1.9930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1344   -1.4082    1.8476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2788   -2.7136    0.9616 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7582   -1.4251   -0.8738 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5722    0.5530   -2.3308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2071    0.1772    1.1434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1155    0.4396   -0.3715 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8587    2.5281    0.7026 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7617    2.2623   -1.0554 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7080    2.8091   -0.4054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8765    3.6736   -0.8262 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3055    1.0955    2.3630 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  3
 16 18  1  0
 18 19  1  0
  7  2  1  0
 18 10  1  0
 18  6  1  0
  1 20  1  0
  1 21  1  0
  6 22  1  0
  7 23  1  0
  8 24  1  0
  8 25  1  0
  9 26  1  0
  9 27  1  0
 11 28  1  0
 11 29  1  0
 11 30  1  0
 12 31  1  0
 13 32  1  0
 14 33  1  0
 14 34  1  0
 15 35  1  0
 15 36  1  0
 17 37  1  0
 17 38  1  0
 19 39  1  0
M  END


  Mrv0541 05061308402D          

 19 21  0  0  0  0            999 V2000
    2.9234   -1.0415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6585    1.3982    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1880    1.8407    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7088   -0.2887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3188    0.4383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8372    1.7892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0126    1.8150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5334   -0.3145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0284    0.8656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2272    1.0622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7534    1.1395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7926    0.3610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0890    0.0428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5780    1.1137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9680    0.3867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3634    1.8665    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7903   -0.3918    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3580   -0.3403    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3252   -0.2691    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  5  4  1  0  0  0  0
  7  6  1  0  0  0  0
  8  1  2  0  0  0  0
  8  4  1  0  0  0  0
  9  2  2  0  0  0  0
 10  6  1  0  0  0  0
 10  9  1  0  0  0  0
 11  5  1  0  0  0  0
 12 10  1  0  0  0  0
 13  9  1  0  0  0  0
 14  3  1  0  0  0  0
 14  7  1  0  0  0  0
 14 11  1  0  0  0  0
 15  8  1  0  0  0  0
 15 12  1  0  0  0  0
 15 14  1  0  0  0  0
 16 11  1  0  0  0  0
 17 13  2  0  0  0  0
 18 15  1  0  0  0  0
 19 12  1  0  0  0  0
 19 13  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0035715

> <DATABASE_NAME>
hmdb

> <SMILES>
CC12CCC3C(OC(=O)C3=C)C1(O)C(=C)CCC2O

> <INCHI_IDENTIFIER>
InChI=1S/C15H20O4/c1-8-4-5-11(16)14(3)7-6-10-9(2)13(17)19-12(10)15(8,14)18/h10-12,16,18H,1-2,4-7H2,3H3

> <INCHI_KEY>
CFUWPZZLCJXNSQ-UHFFFAOYSA-N

> <FORMULA>
C15H20O4

> <MOLECULAR_WEIGHT>
264.3169

> <EXACT_MASS>
264.136159128

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_AVERAGE_POLARIZABILITY>
28.007588816067965

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
6,9a-dihydroxy-5a-methyl-3,9-dimethylidene-dodecahydronaphtho[1,2-b]furan-2-one

> <ALOGPS_LOGP>
0.98

> <JCHEM_LOGP>
1.43558687

> <ALOGPS_LOGS>
-1.77

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.701354924324207

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.859722739922915

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9745770183328837

> <JCHEM_POLAR_SURFACE_AREA>
66.76

> <JCHEM_REFRACTIVITY>
68.779

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.50e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6,9a-dihydroxy-5a-methyl-3,9-dimethylidene-hexahydro-3aH-naphtho[1,2-b]furan-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0035715
     RDKit          3D
Tanacetin
 39 41  0  0  0  0  0  0  0  0999 V2000
    4.4243   -0.6399    0.1832 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1801   -0.3105   -0.0977 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7967    0.5018   -1.2459 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5499    0.9402   -2.1624 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4036    0.7267   -1.1660 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1136    0.6434    0.2148 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9007   -0.6230    0.5862 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3047   -1.8417   -0.0796 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0081   -1.5496   -0.7781 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9424   -0.7597    0.1216 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2250   -1.6691    1.3114 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2006   -0.5130   -0.6816 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8166    0.1587   -1.8438 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1097    0.4393    0.0934 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5350    1.8103   -0.0582 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0348    1.7325    0.0168 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3754    2.7962   -0.4295 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3269    0.5521    0.5533 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4184    0.5863    1.9549 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6789   -1.2559    1.0601 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2675   -0.3394   -0.4087 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5911    1.4544    0.8115 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0111   -0.7346    1.6670 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9836   -2.3009   -0.8264 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0743   -2.5693    0.7503 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1073   -1.1194   -1.7743 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5030   -2.5470   -0.9205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3580   -1.5605    1.9930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1344   -1.4082    1.8476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2788   -2.7136    0.9616 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7582   -1.4251   -0.8738 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5722    0.5530   -2.3308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2071    0.1772    1.1434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1155    0.4396   -0.3715 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8587    2.5281    0.7026 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7617    2.2623   -1.0554 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7080    2.8091   -0.4054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8765    3.6736   -0.8262 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3055    1.0955    2.3630 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  3
 16 18  1  0
 18 19  1  0
  7  2  1  0
 18 10  1  0
 18  6  1  0
  1 20  1  0
  1 21  1  0
  6 22  1  0
  7 23  1  0
  8 24  1  0
  8 25  1  0
  9 26  1  0
  9 27  1  0
 11 28  1  0
 11 29  1  0
 11 30  1  0
 12 31  1  0
 13 32  1  0
 14 33  1  0
 14 34  1  0
 15 35  1  0
 15 36  1  0
 17 37  1  0
 17 38  1  0
 19 39  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       5.457  -1.944   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.563   2.610   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.084   3.436   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.190  -0.539   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.462   0.818   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.163   3.340   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.624   3.388   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.729  -0.587   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.386   1.616   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.891   1.983   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.273   2.127   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.080   0.674   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.499   0.080   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.812   2.079   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.540   0.722   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       2.545   3.484   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0      10.809  -0.731   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0       6.268  -0.635   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       8.074  -0.502   0.000  0.00  0.00           O+0
CONECT    1    8                                                            
CONECT    2    9                                                            
CONECT    3   14                                                            
CONECT    4    5    8                                                       
CONECT    5    4   11                                                       
CONECT    6    7   10                                                       
CONECT    7    6   14                                                       
CONECT    8    1    4   15                                                  
CONECT    9    2   10   13                                                  
CONECT   10    6    9   12                                                  
CONECT   11    5   14   16                                                  
CONECT   12   10   15   19                                                  
CONECT   13    9   17   19                                                  
CONECT   14    3    7   11   15                                             
CONECT   15    8   12   14   18                                             
CONECT   16   11                                                            
CONECT   17   13                                                            
CONECT   18   15                                                            
CONECT   19   12   13                                                       
MASTER        0    0    0    0    0    0    0    0   19    0   42    0
END

COMPND    HMDB0035715
HETATM    1  C1  UNL     1       4.424  -0.640   0.183  1.00  0.00           C  
HETATM    2  C2  UNL     1       3.180  -0.310  -0.098  1.00  0.00           C  
HETATM    3  C3  UNL     1       2.797   0.502  -1.246  1.00  0.00           C  
HETATM    4  O1  UNL     1       3.550   0.940  -2.162  1.00  0.00           O  
HETATM    5  O2  UNL     1       1.404   0.727  -1.166  1.00  0.00           O  
HETATM    6  C4  UNL     1       1.114   0.643   0.215  1.00  0.00           C  
HETATM    7  C5  UNL     1       1.901  -0.623   0.586  1.00  0.00           C  
HETATM    8  C6  UNL     1       1.305  -1.842  -0.080  1.00  0.00           C  
HETATM    9  C7  UNL     1       0.008  -1.550  -0.778  1.00  0.00           C  
HETATM   10  C8  UNL     1      -0.942  -0.760   0.122  1.00  0.00           C  
HETATM   11  C9  UNL     1      -1.225  -1.669   1.311  1.00  0.00           C  
HETATM   12  C10 UNL     1      -2.201  -0.513  -0.682  1.00  0.00           C  
HETATM   13  O3  UNL     1      -1.817   0.159  -1.844  1.00  0.00           O  
HETATM   14  C11 UNL     1      -3.110   0.439   0.093  1.00  0.00           C  
HETATM   15  C12 UNL     1      -2.535   1.810  -0.058  1.00  0.00           C  
HETATM   16  C13 UNL     1      -1.035   1.733   0.017  1.00  0.00           C  
HETATM   17  C14 UNL     1      -0.375   2.796  -0.429  1.00  0.00           C  
HETATM   18  C15 UNL     1      -0.327   0.552   0.553  1.00  0.00           C  
HETATM   19  O4  UNL     1      -0.418   0.586   1.955  1.00  0.00           O  
HETATM   20  H1  UNL     1       4.679  -1.256   1.060  1.00  0.00           H  
HETATM   21  H2  UNL     1       5.268  -0.339  -0.409  1.00  0.00           H  
HETATM   22  H3  UNL     1       1.591   1.454   0.812  1.00  0.00           H  
HETATM   23  H4  UNL     1       2.011  -0.735   1.667  1.00  0.00           H  
HETATM   24  H5  UNL     1       1.984  -2.301  -0.826  1.00  0.00           H  
HETATM   25  H6  UNL     1       1.074  -2.569   0.750  1.00  0.00           H  
HETATM   26  H7  UNL     1       0.107  -1.119  -1.774  1.00  0.00           H  
HETATM   27  H8  UNL     1      -0.503  -2.547  -0.921  1.00  0.00           H  
HETATM   28  H9  UNL     1      -0.358  -1.560   1.993  1.00  0.00           H  
HETATM   29  H10 UNL     1      -2.134  -1.408   1.848  1.00  0.00           H  
HETATM   30  H11 UNL     1      -1.279  -2.714   0.962  1.00  0.00           H  
HETATM   31  H12 UNL     1      -2.758  -1.425  -0.874  1.00  0.00           H  
HETATM   32  H13 UNL     1      -2.572   0.553  -2.331  1.00  0.00           H  
HETATM   33  H14 UNL     1      -3.207   0.177   1.143  1.00  0.00           H  
HETATM   34  H15 UNL     1      -4.115   0.440  -0.371  1.00  0.00           H  
HETATM   35  H16 UNL     1      -2.859   2.528   0.703  1.00  0.00           H  
HETATM   36  H17 UNL     1      -2.762   2.262  -1.055  1.00  0.00           H  
HETATM   37  H18 UNL     1       0.708   2.809  -0.405  1.00  0.00           H  
HETATM   38  H19 UNL     1      -0.876   3.674  -0.826  1.00  0.00           H  
HETATM   39  H20 UNL     1       0.306   1.095   2.363  1.00  0.00           H  
CONECT    1    2    2   20   21
CONECT    2    3    7
CONECT    3    4    4    5
CONECT    5    6
CONECT    6    7   18   22
CONECT    7    8   23
CONECT    8    9   24   25
CONECT    9   10   26   27
CONECT   10   11   12   18
CONECT   11   28   29   30
CONECT   12   13   14   31
CONECT   13   32
CONECT   14   15   33   34
CONECT   15   16   35   36
CONECT   16   17   17   18
CONECT   17   37   38
CONECT   18   19
CONECT   19   39
END

HMDB0035715
     RDKit          3D
Tanacetin
 39 41  0  0  0  0  0  0  0  0999 V2000
    4.4243   -0.6399    0.1832 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1801   -0.3105   -0.0977 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7967    0.5018   -1.2459 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5499    0.9402   -2.1624 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4036    0.7267   -1.1660 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1136    0.6434    0.2148 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9007   -0.6230    0.5862 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3047   -1.8417   -0.0796 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0081   -1.5496   -0.7781 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9424   -0.7597    0.1216 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2250   -1.6691    1.3114 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2006   -0.5130   -0.6816 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8166    0.1587   -1.8438 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1097    0.4393    0.0934 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5350    1.8103   -0.0582 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0348    1.7325    0.0168 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3754    2.7962   -0.4295 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3269    0.5521    0.5533 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4184    0.5863    1.9549 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6789   -1.2559    1.0601 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2675   -0.3394   -0.4087 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5911    1.4544    0.8115 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0111   -0.7346    1.6670 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9836   -2.3009   -0.8264 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0743   -2.5693    0.7503 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1073   -1.1194   -1.7743 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5030   -2.5470   -0.9205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3580   -1.5605    1.9930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1344   -1.4082    1.8476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2788   -2.7136    0.9616 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7582   -1.4251   -0.8738 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5722    0.5530   -2.3308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2071    0.1772    1.1434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1155    0.4396   -0.3715 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8587    2.5281    0.7026 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7617    2.2623   -1.0554 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7080    2.8091   -0.4054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8765    3.6736   -0.8262 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3055    1.0955    2.3630 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  3
 16 18  1  0
 18 19  1  0
  7  2  1  0
 18 10  1  0
 18  6  1  0
  1 20  1  0
  1 21  1  0
  6 22  1  0
  7 23  1  0
  8 24  1  0
  8 25  1  0
  9 26  1  0
  9 27  1  0
 11 28  1  0
 11 29  1  0
 11 30  1  0
 12 31  1  0
 13 32  1  0
 14 33  1  0
 14 34  1  0
 15 35  1  0
 15 36  1  0
 17 37  1  0
 17 38  1  0
 19 39  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
[3AS-(3aalpha,5abeta,6beta,9aalpha,9bbeta)]-decahydro-6,9a-dihydroxy-5a-methyl-3,9-bis(methylene)-naphtho[1,2-b]furan-2(3H)-one	HMDB

Chemical Formula

C₁₅H₂₀O₄

Average Molecular Weight

264.3169

Monoisotopic Molecular Weight

264.136159128

IUPAC Name

6,9a-dihydroxy-5a-methyl-3,9-dimethylidene-dodecahydronaphtho[1,2-b]furan-2-one

Traditional Name

6,9a-dihydroxy-5a-methyl-3,9-dimethylidene-hexahydro-3aH-naphtho[1,2-b]furan-2-one

CAS Registry Number

1401-54-3

SMILES

CC12CCC3C(OC(=O)C3=C)C1(O)C(=C)CCC2O

InChI Identifier

InChI=1S/C15H20O4/c1-8-4-5-11(16)14(3)7-6-10-9(2)13(17)19-12(10)15(8,14)18/h10-12,16,18H,1-2,4-7H2,3H3

InChI Key

CFUWPZZLCJXNSQ-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as eudesmanolides, secoeudesmanolides, and derivatives. These are terpenoids with a structure based on the eudesmanolide (a 3,5a,9-trimethyl-naphtho[1,2-b]furan-2-one derivative) or secoeudesmanolide (a 3,6-dimethyl-5-(pentan-2-yl)-1-benzofuran-2-one derivative) skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Eudesmanolides, secoeudesmanolides, and derivatives

Alternative Parents

Substituents

Eudesmanolide
Sesquiterpenoid
Naphthofuran
Gamma butyrolactone
Cyclic alcohol
Tertiary alcohol
Tetrahydrofuran
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Secondary alcohol
Lactone
Carboxylic acid ester
Oxacycle
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organoheterocyclic compound
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Alcohol
Carbonyl group
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cell membrane (HMDB: HMDB0035715)

Cellular substructure

Route of exposure

Enteral

Ingestion (HMDB: HMDB0035715)

Source

Endogenous

Endogenous (HMDB: HMDB0035715)

Plant

Plant (HMDB: HMDB0035715)

Animal

Animal (HMDB: HMDB0035715)

Exogenous

Food

Food (HMDB: HMDB0035715)

Herb and spice

Herbs and Spices (FooDB: FOOD00866)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid peroxidation (HMDB: HMDB0035715)

Biochemical process

Fatty acid metabolism (HMDB: HMDB0035715)

Cellular process

Cell signaling (HMDB: HMDB0035715)

Biochemical pathway

Lipid metabolism pathway (HMDB: HMDB0035715)

Role

Biological role

Membrane stabilizer (HMDB: HMDB0035715)

Nutrient

Nutrient (HMDB: HMDB0035715)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0035715)

Emulsifier (HMDB: HMDB0035715)

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	205 - 206 °C	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	4786 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	4.5 g/L	ALOGPS
logP	0.98	ALOGPS
logP	1.44	ChemAxon
logS	-1.8	ALOGPS
pKa (Strongest Acidic)	12.86	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	66.76 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	68.78 m³·mol⁻¹	ChemAxon
Polarizability	28.01 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	160.969	31661259
DarkChem	[M-H]-	154.608	31661259
DeepCCS	[M-2H]-	195.673	30932474
DeepCCS	[M+Na]+	171.239	30932474
AllCCS	[M+H]+	162.6	32859911
AllCCS	[M+H-H2O]+	159.1	32859911
AllCCS	[M+NH4]+	166.0	32859911
AllCCS	[M+Na]+	166.9	32859911
AllCCS	[M-H]-	165.8	32859911
AllCCS	[M+Na-2H]-	165.7	32859911
AllCCS	[M+HCOO]-	165.8	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Tanacetin	CC12CCC3C(OC(=O)C3=C)C1(O)C(=C)CCC2O	3362.2	Standard polar	33892256
Tanacetin	CC12CCC3C(OC(=O)C3=C)C1(O)C(=C)CCC2O	2182.9	Standard non polar	33892256
Tanacetin	CC12CCC3C(OC(=O)C3=C)C1(O)C(=C)CCC2O	2382.7	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Tanacetin,1TMS,isomer #1	C=C1C(=O)OC2C1CCC1(C)C(O)CCC(=C)C21O[Si](C)(C)C	2192.0	Semi standard non polar	33892256
Tanacetin,1TMS,isomer #2	C=C1C(=O)OC2C1CCC1(C)C(O[Si](C)(C)C)CCC(=C)C21O	2220.3	Semi standard non polar	33892256
Tanacetin,2TMS,isomer #1	C=C1C(=O)OC2C1CCC1(C)C(O[Si](C)(C)C)CCC(=C)C21O[Si](C)(C)C	2240.9	Semi standard non polar	33892256
Tanacetin,1TBDMS,isomer #1	C=C1C(=O)OC2C1CCC1(C)C(O)CCC(=C)C21O[Si](C)(C)C(C)(C)C	2416.5	Semi standard non polar	33892256
Tanacetin,1TBDMS,isomer #2	C=C1C(=O)OC2C1CCC1(C)C(O[Si](C)(C)C(C)(C)C)CCC(=C)C21O	2450.6	Semi standard non polar	33892256
Tanacetin,2TBDMS,isomer #1	C=C1C(=O)OC2C1CCC1(C)C(O[Si](C)(C)C(C)(C)C)CCC(=C)C21O[Si](C)(C)C(C)(C)C	2685.0	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 - Tanacetin GC-MS (Non-derivatized) - 70eV, Positive	splash10-0uyi-9720000000-2687944479c5c1ab5258	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tanacetin GC-MS (2 TMS) - 70eV, Positive	splash10-00uv-9278000000-713a4dce9ecc1e2b2b40	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tanacetin 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 - Tanacetin 10V, Negative-QTOF	splash10-03di-0090000000-1829d2bf51361905839e	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tanacetin 20V, Negative-QTOF	splash10-03xs-0090000000-5bbaca27e944b63e77f7	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tanacetin 40V, Negative-QTOF	splash10-0uxr-9480000000-f790027821c6ba7ea252	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tanacetin 10V, Negative-QTOF	splash10-03di-0090000000-16d43704d08f3756e03a	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tanacetin 20V, Negative-QTOF	splash10-03xr-0090000000-7731f5b3032c1efbd002	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tanacetin 40V, Negative-QTOF	splash10-002f-2930000000-f50b50e38e0f2dc18b3c	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tanacetin 10V, Positive-QTOF	splash10-00kb-0190000000-62ab0be2aabe7eae7a5a	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tanacetin 20V, Positive-QTOF	splash10-00mn-1690000000-d586f2dadc430340fcb0	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tanacetin 40V, Positive-QTOF	splash10-0ufr-9630000000-c9f54aa4b1a34a6eeaf2	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tanacetin 10V, Positive-QTOF	splash10-014i-0190000000-80e1ef101119bdf0108a	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tanacetin 20V, Positive-QTOF	splash10-014j-0490000000-4af01ecdfb833bb406a1	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tanacetin 40V, Positive-QTOF	splash10-01b9-4900000000-3518bf49f616cbfeb48a	2021-09-23	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Cytoplasm
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

FDB014439

KNApSAcK ID

C00012967

Chemspider ID

35014001

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

73656854

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

rw1851131

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 Tanacetin (HMDB0035715)

MOL for HMDB0035715 (Tanacetin)

3D MOL for HMDB0035715 (Tanacetin)

3D SDF for HMDB0035715 (Tanacetin)

3D-SDF for HMDB0035715 (Tanacetin)

PDB for HMDB0035715 (Tanacetin)

3D PDB for HMDB0035715 (Tanacetin)

SMILES for HMDB0035715 (Tanacetin)

INCHI for HMDB0035715 (Tanacetin)

Structure for HMDB0035715 (Tanacetin)

3D Structure for HMDB0035715 (Tanacetin)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra