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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-12 00:08:24 UTC

Update Date

2022-03-07 02:55:55 UTC

HMDB ID

HMDB0038795

Secondary Accession Numbers

HMDB38795

Metabolite Identification

Common Name

7,9-Illudadiene-3,14-diol

Description

7,9-Illudadiene-3,14-diol belongs to the class of organic compounds known as illudanes and illudins. These are sesquiterpenoids containing either the illudane moiety (based on a 3,6,6,7b-tetramethyl-decahydro-1H-cyclobuta[e]indene ring system), the illudin moiety (2',2',4',6'-tetramethyl-octahydrospiro[cyclopropane-1,5'-indene]), or a derivative thereof. Based on a literature review a small amount of articles have been published on 7,9-Illudadiene-3,14-diol.

Structure

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

HMDB0038795
     RDKit          3D
7,9-Illudadiene-3,14-diol
 39 41  0  0  0  0  0  0  0  0999 V2000
   -3.6193    0.4299   -0.3296 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5807   -0.2010    0.5359 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1494   -1.0019    1.6811 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7122    0.8678    1.0849 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6083    0.9588    0.3555 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5491    1.8296    0.4654 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7418    1.3066    0.2404 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9885    2.1126    0.3263 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7223    3.4187    0.6588 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7609   -0.1512   -0.0969 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0273   -1.0252    1.0778 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0374   -0.9037   -0.0209 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7034   -0.4854   -1.1170 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7709   -1.9574   -1.4533 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1229    0.1689   -2.3044 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6431   -0.0133   -0.7543 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5974   -1.0587   -0.2700 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3597    1.4863   -0.6001 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5702    0.4834    0.2730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8456   -0.1620   -1.2172 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9038   -1.7106    1.3408 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5697   -0.2843    2.4098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3035   -1.5742    2.1300 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9546    1.4706    1.9390 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4381    2.8828    0.7342 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6647    1.5963    1.0289 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4952    2.0991   -0.6702 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8003    4.0437   -0.1116 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2903   -0.5525    2.0714 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5574   -2.0028    1.2263 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9836   -0.3976    0.2625 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2165   -1.7562   -0.7061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0443   -2.2199   -2.1844 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6860   -2.5253   -0.5300 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7100   -2.1200   -2.0229 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6628   -0.2103   -3.0937 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1203    0.4356   -1.6695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1677   -1.4948   -1.1121 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1795   -1.7825    0.4222 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  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  7 10  1  0
 10 11  1  0
 11 12  1  0
 10 13  1  0
 13 14  1  0
 13 15  1  0
 13 16  1  0
 16 17  1  0
 17  2  1  0
 16  5  1  0
 12 10  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  3 21  1  0
  3 22  1  0
  3 23  1  0
  4 24  1  0
  6 25  1  0
  8 26  1  0
  8 27  1  0
  9 28  1  0
 11 29  1  0
 11 30  1  0
 12 31  1  0
 12 32  1  0
 14 33  1  0
 14 34  1  0
 14 35  1  0
 15 36  1  0
 16 37  1  0
 17 38  1  0
 17 39  1  0
M  END


  Mrv0541 05061310392D          

 17 19  0  0  0  0            999 V2000
    4.6233    1.5237    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3355    2.5896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0803    2.6478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5903    2.1737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3783    1.3763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1872    0.5830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5934    1.1260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2453    2.4147    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8077    0.2105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7694    1.1675    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3899    0.7950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5543    1.9640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8875    1.8968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7570    2.1760    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1748    1.5914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0228   -0.5860    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1042    2.9244    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  5  4  1  0  0  0  0
 10  6  1  0  0  0  0
 10  7  2  0  0  0  0
 11  6  2  0  0  0  0
 11  9  1  0  0  0  0
 12  8  1  0  0  0  0
 12 10  1  0  0  0  0
 13  1  1  0  0  0  0
 13  2  1  0  0  0  0
 13  7  1  0  0  0  0
 13  8  1  0  0  0  0
 14  3  1  0  0  0  0
 14 12  1  0  0  0  0
 15  4  1  0  0  0  0
 15  5  1  0  0  0  0
 15 11  1  0  0  0  0
 15 14  1  0  0  0  0
 16  9  1  0  0  0  0
 17 14  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0038795

> <DATABASE_NAME>
hmdb

> <SMILES>
CC1(C)CC2C(=C1)C=C(CO)C1(CC1)C2(C)O

> <INCHI_IDENTIFIER>
InChI=1S/C15H22O2/c1-13(2)7-10-6-11(9-16)15(4-5-15)14(3,17)12(10)8-13/h6-7,12,16-17H,4-5,8-9H2,1-3H3

> <INCHI_KEY>
YEDYYAKSTVQMBN-UHFFFAOYSA-N

> <FORMULA>
C15H22O2

> <MOLECULAR_WEIGHT>
234.334

> <EXACT_MASS>
234.161979948

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_AVERAGE_POLARIZABILITY>
27.213891774704685

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
6'-(hydroxymethyl)-2',2',4'-trimethyl-2',3',3'a,4'-tetrahydrospiro[cyclopropane-1,5'-indene]-4'-ol

> <ALOGPS_LOGP>
2.06

> <JCHEM_LOGP>
1.2555077833333335

> <ALOGPS_LOGS>
-2.51

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.177187259947548

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.156565903824454

> <JCHEM_PKA_STRONGEST_BASIC>
-2.7453262864191963

> <JCHEM_POLAR_SURFACE_AREA>
40.46

> <JCHEM_REFRACTIVITY>
69.84719999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.29e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6'-(hydroxymethyl)-2',2',4'-trimethyl-3',3'a-dihydrospiro[cyclopropane-1,5'-indene]-4'-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0038795
     RDKit          3D
7,9-Illudadiene-3,14-diol
 39 41  0  0  0  0  0  0  0  0999 V2000
   -3.6193    0.4299   -0.3296 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5807   -0.2010    0.5359 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1494   -1.0019    1.6811 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7122    0.8678    1.0849 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6083    0.9588    0.3555 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5491    1.8296    0.4654 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7418    1.3066    0.2404 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9885    2.1126    0.3263 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7223    3.4187    0.6588 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7609   -0.1512   -0.0969 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0273   -1.0252    1.0778 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0374   -0.9037   -0.0209 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7034   -0.4854   -1.1170 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7709   -1.9574   -1.4533 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1229    0.1689   -2.3044 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6431   -0.0133   -0.7543 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5974   -1.0587   -0.2700 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3597    1.4863   -0.6001 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5702    0.4834    0.2730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8456   -0.1620   -1.2172 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9038   -1.7106    1.3408 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5697   -0.2843    2.4098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3035   -1.5742    2.1300 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9546    1.4706    1.9390 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4381    2.8828    0.7342 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6647    1.5963    1.0289 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4952    2.0991   -0.6702 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8003    4.0437   -0.1116 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2903   -0.5525    2.0714 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5574   -2.0028    1.2263 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9836   -0.3976    0.2625 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2165   -1.7562   -0.7061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0443   -2.2199   -2.1844 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6860   -2.5253   -0.5300 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7100   -2.1200   -2.0229 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6628   -0.2103   -3.0937 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1203    0.4356   -1.6695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1677   -1.4948   -1.1121 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1795   -1.7825    0.4222 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  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  7 10  1  0
 10 11  1  0
 11 12  1  0
 10 13  1  0
 13 14  1  0
 13 15  1  0
 13 16  1  0
 16 17  1  0
 17  2  1  0
 16  5  1  0
 12 10  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  3 21  1  0
  3 22  1  0
  3 23  1  0
  4 24  1  0
  6 25  1  0
  8 26  1  0
  8 27  1  0
  9 28  1  0
 11 29  1  0
 11 30  1  0
 12 31  1  0
 12 32  1  0
 14 33  1  0
 14 34  1  0
 14 35  1  0
 15 36  1  0
 16 37  1  0
 17 38  1  0
 17 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       8.630   2.844   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.093   4.834   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.017   4.943   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.102   4.058   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.706   2.569   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.083   1.088   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.708   2.102   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.058   4.507   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.508   0.393   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.170   2.179   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.594   1.484   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.768   3.666   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.257   3.541   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.280   4.062   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.193   2.971   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       1.909  -1.094   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       3.928   5.459   0.000  0.00  0.00           O+0
CONECT    1   13                                                            
CONECT    2   13                                                            
CONECT    3   14                                                            
CONECT    4    5   15                                                       
CONECT    5    4   15                                                       
CONECT    6   10   11                                                       
CONECT    7   10   13                                                       
CONECT    8   12   13                                                       
CONECT    9   11   16                                                       
CONECT   10    6    7   12                                                  
CONECT   11    6    9   15                                                  
CONECT   12    8   10   14                                                  
CONECT   13    1    2    7    8                                             
CONECT   14    3   12   15   17                                             
CONECT   15    4    5   11   14                                             
CONECT   16    9                                                            
CONECT   17   14                                                            
MASTER        0    0    0    0    0    0    0    0   17    0   38    0
END

COMPND    HMDB0038795
HETATM    1  C1  UNL     1      -3.619   0.430  -0.330  1.00  0.00           C  
HETATM    2  C2  UNL     1      -2.581  -0.201   0.536  1.00  0.00           C  
HETATM    3  C3  UNL     1      -3.149  -1.002   1.681  1.00  0.00           C  
HETATM    4  C4  UNL     1      -1.712   0.868   1.085  1.00  0.00           C  
HETATM    5  C5  UNL     1      -0.608   0.959   0.355  1.00  0.00           C  
HETATM    6  C6  UNL     1       0.549   1.830   0.465  1.00  0.00           C  
HETATM    7  C7  UNL     1       1.742   1.307   0.240  1.00  0.00           C  
HETATM    8  C8  UNL     1       2.989   2.113   0.326  1.00  0.00           C  
HETATM    9  O1  UNL     1       2.722   3.419   0.659  1.00  0.00           O  
HETATM   10  C9  UNL     1       1.761  -0.151  -0.097  1.00  0.00           C  
HETATM   11  C10 UNL     1       2.027  -1.025   1.078  1.00  0.00           C  
HETATM   12  C11 UNL     1       3.037  -0.904  -0.021  1.00  0.00           C  
HETATM   13  C12 UNL     1       0.703  -0.485  -1.117  1.00  0.00           C  
HETATM   14  C13 UNL     1       0.771  -1.957  -1.453  1.00  0.00           C  
HETATM   15  O2  UNL     1       1.123   0.169  -2.304  1.00  0.00           O  
HETATM   16  C14 UNL     1      -0.643  -0.013  -0.754  1.00  0.00           C  
HETATM   17  C15 UNL     1      -1.597  -1.059  -0.270  1.00  0.00           C  
HETATM   18  H1  UNL     1      -3.360   1.486  -0.600  1.00  0.00           H  
HETATM   19  H2  UNL     1      -4.570   0.483   0.273  1.00  0.00           H  
HETATM   20  H3  UNL     1      -3.846  -0.162  -1.217  1.00  0.00           H  
HETATM   21  H4  UNL     1      -3.904  -1.711   1.341  1.00  0.00           H  
HETATM   22  H5  UNL     1      -3.570  -0.284   2.410  1.00  0.00           H  
HETATM   23  H6  UNL     1      -2.304  -1.574   2.130  1.00  0.00           H  
HETATM   24  H7  UNL     1      -1.955   1.471   1.939  1.00  0.00           H  
HETATM   25  H8  UNL     1       0.438   2.883   0.734  1.00  0.00           H  
HETATM   26  H9  UNL     1       3.665   1.596   1.029  1.00  0.00           H  
HETATM   27  H10 UNL     1       3.495   2.099  -0.670  1.00  0.00           H  
HETATM   28  H11 UNL     1       2.800   4.044  -0.112  1.00  0.00           H  
HETATM   29  H12 UNL     1       2.290  -0.553   2.071  1.00  0.00           H  
HETATM   30  H13 UNL     1       1.557  -2.003   1.226  1.00  0.00           H  
HETATM   31  H14 UNL     1       3.984  -0.398   0.262  1.00  0.00           H  
HETATM   32  H15 UNL     1       3.217  -1.756  -0.706  1.00  0.00           H  
HETATM   33  H16 UNL     1      -0.044  -2.220  -2.184  1.00  0.00           H  
HETATM   34  H17 UNL     1       0.686  -2.525  -0.530  1.00  0.00           H  
HETATM   35  H18 UNL     1       1.710  -2.120  -2.023  1.00  0.00           H  
HETATM   36  H19 UNL     1       0.663  -0.210  -3.094  1.00  0.00           H  
HETATM   37  H20 UNL     1      -1.120   0.436  -1.669  1.00  0.00           H  
HETATM   38  H21 UNL     1      -2.168  -1.495  -1.112  1.00  0.00           H  
HETATM   39  H22 UNL     1      -1.179  -1.782   0.422  1.00  0.00           H  
CONECT    1    2   18   19   20
CONECT    2    3    4   17
CONECT    3   21   22   23
CONECT    4    5    5   24
CONECT    5    6   16
CONECT    6    7    7   25
CONECT    7    8   10
CONECT    8    9   26   27
CONECT    9   28
CONECT   10   11   12   13
CONECT   11   12   29   30
CONECT   12   31   32
CONECT   13   14   15   16
CONECT   14   33   34   35
CONECT   15   36
CONECT   16   17   37
CONECT   17   38   39
END

HMDB0038795
     RDKit          3D
7,9-Illudadiene-3,14-diol
 39 41  0  0  0  0  0  0  0  0999 V2000
   -3.6193    0.4299   -0.3296 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5807   -0.2010    0.5359 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1494   -1.0019    1.6811 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7122    0.8678    1.0849 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6083    0.9588    0.3555 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5491    1.8296    0.4654 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7418    1.3066    0.2404 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9885    2.1126    0.3263 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7223    3.4187    0.6588 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7609   -0.1512   -0.0969 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0273   -1.0252    1.0778 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0374   -0.9037   -0.0209 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7034   -0.4854   -1.1170 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7709   -1.9574   -1.4533 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1229    0.1689   -2.3044 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6431   -0.0133   -0.7543 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5974   -1.0587   -0.2700 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3597    1.4863   -0.6001 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5702    0.4834    0.2730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8456   -0.1620   -1.2172 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9038   -1.7106    1.3408 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5697   -0.2843    2.4098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3035   -1.5742    2.1300 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9546    1.4706    1.9390 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4381    2.8828    0.7342 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6647    1.5963    1.0289 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4952    2.0991   -0.6702 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8003    4.0437   -0.1116 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2903   -0.5525    2.0714 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5574   -2.0028    1.2263 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9836   -0.3976    0.2625 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2165   -1.7562   -0.7061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0443   -2.2199   -2.1844 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6860   -2.5253   -0.5300 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7100   -2.1200   -2.0229 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6628   -0.2103   -3.0937 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1203    0.4356   -1.6695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1677   -1.4948   -1.1121 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1795   -1.7825    0.4222 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  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  7 10  1  0
 10 11  1  0
 11 12  1  0
 10 13  1  0
 13 14  1  0
 13 15  1  0
 13 16  1  0
 16 17  1  0
 17  2  1  0
 16  5  1  0
 12 10  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  3 21  1  0
  3 22  1  0
  3 23  1  0
  4 24  1  0
  6 25  1  0
  8 26  1  0
  8 27  1  0
  9 28  1  0
 11 29  1  0
 11 30  1  0
 12 31  1  0
 12 32  1  0
 14 33  1  0
 14 34  1  0
 14 35  1  0
 15 36  1  0
 16 37  1  0
 17 38  1  0
 17 39  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₁₅H₂₂O₂

Average Molecular Weight

234.334

Monoisotopic Molecular Weight

234.161979948

IUPAC Name

6'-(hydroxymethyl)-2',2',4'-trimethyl-2',3',3'a,4'-tetrahydrospiro[cyclopropane-1,5'-indene]-4'-ol

Traditional Name

6'-(hydroxymethyl)-2',2',4'-trimethyl-3',3'a-dihydrospiro[cyclopropane-1,5'-indene]-4'-ol

CAS Registry Number

141940-51-4

SMILES

CC1(C)CC2C(=C1)C=C(CO)C1(CC1)C2(C)O

InChI Identifier

InChI=1S/C15H22O2/c1-13(2)7-10-6-11(9-16)15(4-5-15)14(3,17)12(10)8-13/h6-7,12,16-17H,4-5,8-9H2,1-3H3

InChI Key

YEDYYAKSTVQMBN-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as illudanes and illudins. These are sesquiterpenoids containing either the illudane moiety (based on a 3,6,6,7b-tetramethyl-decahydro-1H-cyclobuta[e]indene ring system), the illudin moiety (2',2',4',6'-tetramethyl-octahydrospiro[cyclopropane-1,5'-indene]), or a derivative thereof.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Illudanes and illudins

Alternative Parents

Substituents

Illudine sesquiterpenoid
Tertiary alcohol
Organic oxygen compound
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cell membrane (HMDB: HMDB0038795)

Cellular substructure

Route of exposure

Enteral

Ingestion (HMDB: HMDB0038795)

Source

Endogenous

Endogenous (HMDB: HMDB0038795)

Plant

Plant (HMDB: HMDB0038795)

Animal

Animal (HMDB: HMDB0038795)

Exogenous

Food

Food (HMDB: HMDB0038795)

Vegetable

Mushroom

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid peroxidation (HMDB: HMDB0038795)

Biochemical process

Fatty acid metabolism (HMDB: HMDB0038795)

Cellular process

Cell signaling (HMDB: HMDB0038795)

Biochemical pathway

Lipid metabolism pathway (HMDB: HMDB0038795)

Role

Biological role

Membrane stabilizer (HMDB: HMDB0038795)

Nutrient

Nutrient (HMDB: HMDB0038795)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0038795)

Emulsifier (HMDB: HMDB0038795)

Physical Properties

State

Not Available

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.73 g/L	ALOGPS
logP	2.06	ALOGPS
logP	1.26	ChemAxon
logS	-2.5	ALOGPS
pKa (Strongest Acidic)	14.16	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	40.46 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	69.85 m³·mol⁻¹	ChemAxon
Polarizability	27.21 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]+	154.453	31661259
DarkChem	[M-H]-	153.453	31661259
DeepCCS	[M+H]+	165.78	30932474
DeepCCS	[M-H]-	163.422	30932474
DeepCCS	[M-2H]-	196.308	30932474
DeepCCS	[M+Na]+	171.873	30932474
AllCCS	[M+H]+	154.9	32859911
AllCCS	[M+H-H2O]+	151.2	32859911
AllCCS	[M+NH4]+	158.3	32859911
AllCCS	[M+Na]+	159.3	32859911
AllCCS	[M-H]-	162.1	32859911
AllCCS	[M+Na-2H]-	162.3	32859911
AllCCS	[M+HCOO]-	162.6	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
7,9-Illudadiene-3,14-diol	CC1(C)CC2C(=C1)C=C(CO)C1(CC1)C2(C)O	2983.7	Standard polar	33892256
7,9-Illudadiene-3,14-diol	CC1(C)CC2C(=C1)C=C(CO)C1(CC1)C2(C)O	1866.5	Standard non polar	33892256
7,9-Illudadiene-3,14-diol	CC1(C)CC2C(=C1)C=C(CO)C1(CC1)C2(C)O	1874.9	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
7,9-Illudadiene-3,14-diol,1TMS,isomer #1	CC1(C)C=C2C=C(CO[Si](C)(C)C)C3(CC3)C(C)(O)C2C1	1922.4	Semi standard non polar	33892256
7,9-Illudadiene-3,14-diol,1TMS,isomer #2	CC1(C)C=C2C=C(CO)C3(CC3)C(C)(O[Si](C)(C)C)C2C1	1969.4	Semi standard non polar	33892256
7,9-Illudadiene-3,14-diol,2TMS,isomer #1	CC1(C)C=C2C=C(CO[Si](C)(C)C)C3(CC3)C(C)(O[Si](C)(C)C)C2C1	1975.7	Semi standard non polar	33892256
7,9-Illudadiene-3,14-diol,1TBDMS,isomer #1	CC1(C)C=C2C=C(CO[Si](C)(C)C(C)(C)C)C3(CC3)C(C)(O)C2C1	2166.6	Semi standard non polar	33892256
7,9-Illudadiene-3,14-diol,1TBDMS,isomer #2	CC1(C)C=C2C=C(CO)C3(CC3)C(C)(O[Si](C)(C)C(C)(C)C)C2C1	2219.5	Semi standard non polar	33892256
7,9-Illudadiene-3,14-diol,2TBDMS,isomer #1	CC1(C)C=C2C=C(CO[Si](C)(C)C(C)(C)C)C3(CC3)C(C)(O[Si](C)(C)C(C)(C)C)C2C1	2429.1	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 - 7,9-Illudadiene-3,14-diol GC-MS (Non-derivatized) - 70eV, Positive	splash10-0gdr-3930000000-24fc050a6ee707d9440f	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,9-Illudadiene-3,14-diol GC-MS (2 TMS) - 70eV, Positive	splash10-03fr-7098000000-2d6285a16ec547b2fc08	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,9-Illudadiene-3,14-diol 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 - 7,9-Illudadiene-3,14-diol 10V, Positive-QTOF	splash10-014r-1390000000-b87bdc0c97106f36486b	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 7,9-Illudadiene-3,14-diol 20V, Positive-QTOF	splash10-014s-8980000000-e4830dce9c13b79b96bb	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 7,9-Illudadiene-3,14-diol 40V, Positive-QTOF	splash10-000l-9300000000-675bbb7d48aeaa02ee69	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 7,9-Illudadiene-3,14-diol 10V, Negative-QTOF	splash10-001i-0090000000-9b5384fb8d0d731f6247	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 7,9-Illudadiene-3,14-diol 20V, Negative-QTOF	splash10-0fsi-0290000000-cd85e5ec7f9015c6dfca	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 7,9-Illudadiene-3,14-diol 40V, Negative-QTOF	splash10-000i-7940000000-19558cef7a5bbdb6b07c	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 7,9-Illudadiene-3,14-diol 10V, Negative-QTOF	splash10-001i-0090000000-ee56b8a065eb4a8064ba	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 7,9-Illudadiene-3,14-diol 20V, Negative-QTOF	splash10-001i-0190000000-721cbc0fe5ed355a490f	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 7,9-Illudadiene-3,14-diol 40V, Negative-QTOF	splash10-001r-2690000000-f29d0f68707ff4404274	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 7,9-Illudadiene-3,14-diol 10V, Positive-QTOF	splash10-000i-0190000000-7deea30f35d37a528c2b	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 7,9-Illudadiene-3,14-diol 20V, Positive-QTOF	splash10-000i-1590000000-6b9fb33493da156ed8e9	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 7,9-Illudadiene-3,14-diol 40V, Positive-QTOF	splash10-000l-9270000000-c722673261c8856fcc4b	2021-09-23	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

FDB018220

KNApSAcK ID

Not Available

Chemspider ID

35014666

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

91752244

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 7,9-Illudadiene-3,14-diol (HMDB0038795)

MOL for HMDB0038795 (7,9-Illudadiene-3,14-diol)

3D MOL for HMDB0038795 (7,9-Illudadiene-3,14-diol)

3D SDF for HMDB0038795 (7,9-Illudadiene-3,14-diol)

3D-SDF for HMDB0038795 (7,9-Illudadiene-3,14-diol)

PDB for HMDB0038795 (7,9-Illudadiene-3,14-diol)

3D PDB for HMDB0038795 (7,9-Illudadiene-3,14-diol)

SMILES for HMDB0038795 (7,9-Illudadiene-3,14-diol)

INCHI for HMDB0038795 (7,9-Illudadiene-3,14-diol)

Structure for HMDB0038795 (7,9-Illudadiene-3,14-diol)

3D Structure for HMDB0038795 (7,9-Illudadiene-3,14-diol)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra