Jump To Section:

Identification Taxonomy Ontology Physical properties Spectra Biological properties Concentrations Links References XML

Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 23:04:07 UTC

Update Date

2022-03-07 02:55:31 UTC

HMDB ID

HMDB0037809

Secondary Accession Numbers

HMDB37809

Metabolite Identification

Common Name

Hexahydro-2',3alpha-dimethylspiro[1,3-dithiolo[4,5-b]furan-2,3'(2'H)-furan]

Description

Hexahydro-2',3alpha-dimethylspiro[1,3-dithiolo[4,5-b]furan-2,3'(2'H)-furan] belongs to the class of organic compounds known as monothioketals. Monothioketals are compounds containing a monothioketal functional group with the general structure R2C(OR')(SR') with (R = any atom but H). Hexahydro-2',3alpha-dimethylspiro[1,3-dithiolo[4,5-b]furan-2,3'(2'H)-furan] is a meaty tasting compound. Based on a literature review very few articles have been published on Hexahydro-2',3alpha-dimethylspiro[1,3-dithiolo[4,5-b]furan-2,3'(2'H)-furan].

Structure

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

HMDB0037809
     RDKit          3D
Hexahydro-2',3alpha-dimethylspiro[1,3-dithiolo[4,5-b]furan-2,3'(2'H)-furan]
 30 32  0  0  0  0  0  0  0  0999 V2000
   -2.5190   -1.7845   -0.2707 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3261   -0.4902    0.4762 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4241    0.3406    0.4353 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1585    1.4045   -0.3891 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6431    1.6163   -0.3755 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1502    0.2944    0.0610 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1398    0.4059    1.3661 S   0  0  0  0  0  0  0  0  0  0  0  0
    1.3177   -0.7506    0.7300 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7099   -0.6774    1.1542 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4565   -0.7650   -0.1886 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4509   -1.0144   -1.1581 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4497   -0.2192   -0.7160 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8198    1.2389   -0.5912 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1968   -0.5012   -1.2955 S   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7179   -1.6656   -1.3352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3476   -2.3460    0.2276 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6009   -2.4013   -0.0654 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1879   -0.7776    1.5600 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6604    2.3380   -0.0976 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4840    1.1093   -1.4276 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3571    2.4111    0.3388 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3599    1.8648   -1.4194 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8893   -1.7707    0.7012 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0309    0.1598    1.7565 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9810   -1.6207    1.7052 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1992   -1.5635   -0.1924 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8705    0.2344   -0.4408 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5365    1.5427   -1.3976 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3313    1.4776    0.3623 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9504    1.9096   -0.6696 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  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
 11 12  1  0
 12 13  1  0
 12 14  1  0
  6  2  1  0
 12  8  1  0
 14  6  1  0
  1 15  1  0
  1 16  1  0
  1 17  1  0
  2 18  1  0
  4 19  1  0
  4 20  1  0
  5 21  1  0
  5 22  1  0
  8 23  1  0
  9 24  1  0
  9 25  1  0
 10 26  1  0
 10 27  1  0
 13 28  1  0
 13 29  1  0
 13 30  1  0
M  END


  Mrv0541 05061310012D          

 14 16  0  0  0  0            999 V2000
    1.4733    0.2953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9728    2.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7574    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2183    2.4148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2424    1.7474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4337    2.1599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2183    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9728    1.3349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9728    2.1599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7033    1.7474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4337    1.3349    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7574    2.4148    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1882    1.0799    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    2.1882    2.4148    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
  5  3  1  0  0  0  0
  6  4  1  0  0  0  0
  7  1  1  0  0  0  0
  8  3  1  0  0  0  0
  9  2  1  0  0  0  0
  9  8  1  0  0  0  0
 10  4  1  0  0  0  0
 10  7  1  0  0  0  0
 11  6  1  0  0  0  0
 11  7  1  0  0  0  0
 12  5  1  0  0  0  0
 12  9  1  0  0  0  0
 13  8  1  0  0  0  0
 13 10  1  0  0  0  0
 14  9  1  0  0  0  0
 14 10  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0037809

> <DATABASE_NAME>
hmdb

> <SMILES>
CC1OCCC11SC2CCOC2(C)S1

> <INCHI_IDENTIFIER>
InChI=1S/C10H16O2S2/c1-7-10(4-6-11-7)13-8-3-5-12-9(8,2)14-10/h7-8H,3-6H2,1-2H3

> <INCHI_KEY>
LGPJANFPSFABDB-UHFFFAOYSA-N

> <FORMULA>
C10H16O2S2

> <MOLECULAR_WEIGHT>
232.363

> <EXACT_MASS>
232.059171136

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_AVERAGE_POLARIZABILITY>
24.275182806474636

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2',3a-dimethyl-tetrahydrospiro[[1,3]dithiolo[4,5-b]furan-2,3'-oxolane]

> <ALOGPS_LOGP>
2.09

> <JCHEM_LOGP>
2.273976933666666

> <ALOGPS_LOGS>
-3.11

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-3.8985954242543825

> <JCHEM_POLAR_SURFACE_AREA>
18.46

> <JCHEM_REFRACTIVITY>
60.67860000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.82e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2',3a-dimethyl-dihydro-5H-spiro[[1,3]dithiolo[4,5-b]furan-2,3'-oxolane]

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0037809
     RDKit          3D
Hexahydro-2',3alpha-dimethylspiro[1,3-dithiolo[4,5-b]furan-2,3'(2'H)-furan]
 30 32  0  0  0  0  0  0  0  0999 V2000
   -2.5190   -1.7845   -0.2707 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3261   -0.4902    0.4762 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4241    0.3406    0.4353 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1585    1.4045   -0.3891 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6431    1.6163   -0.3755 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1502    0.2944    0.0610 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1398    0.4059    1.3661 S   0  0  0  0  0  0  0  0  0  0  0  0
    1.3177   -0.7506    0.7300 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7099   -0.6774    1.1542 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4565   -0.7650   -0.1886 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4509   -1.0144   -1.1581 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4497   -0.2192   -0.7160 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8198    1.2389   -0.5912 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1968   -0.5012   -1.2955 S   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7179   -1.6656   -1.3352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3476   -2.3460    0.2276 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6009   -2.4013   -0.0654 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1879   -0.7776    1.5600 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6604    2.3380   -0.0976 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4840    1.1093   -1.4276 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3571    2.4111    0.3388 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3599    1.8648   -1.4194 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8893   -1.7707    0.7012 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0309    0.1598    1.7565 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9810   -1.6207    1.7052 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1992   -1.5635   -0.1924 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8705    0.2344   -0.4408 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5365    1.5427   -1.3976 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3313    1.4776    0.3623 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9504    1.9096   -0.6696 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  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
 11 12  1  0
 12 13  1  0
 12 14  1  0
  6  2  1  0
 12  8  1  0
 14  6  1  0
  1 15  1  0
  1 16  1  0
  1 17  1  0
  2 18  1  0
  4 19  1  0
  4 20  1  0
  5 21  1  0
  5 22  1  0
  8 23  1  0
  9 24  1  0
  9 25  1  0
 10 26  1  0
 10 27  1  0
 13 28  1  0
 13 29  1  0
 13 30  1  0
M  END

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0       2.750   0.551   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.549   5.572   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.014   2.016   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.274   4.508   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.919   3.262   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.810   4.032   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.274   2.016   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.549   2.492   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.549   4.032   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.179   3.262   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       0.810   2.492   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0       7.014   4.508   0.000  0.00  0.00           O+0
HETATM   13  S   UNK     0       4.085   2.016   0.000  0.00  0.00           S+0
HETATM   14  S   UNK     0       4.085   4.508   0.000  0.00  0.00           S+0
CONECT    1    7                                                            
CONECT    2    9                                                            
CONECT    3    5    8                                                       
CONECT    4    6   10                                                       
CONECT    5    3   12                                                       
CONECT    6    4   11                                                       
CONECT    7    1   10   11                                                  
CONECT    8    3    9   13                                                  
CONECT    9    2    8   12   14                                             
CONECT   10    4    7   13   14                                             
CONECT   11    6    7                                                       
CONECT   12    5    9                                                       
CONECT   13    8   10                                                       
CONECT   14    9   10                                                       
MASTER        0    0    0    0    0    0    0    0   14    0   32    0
END

COMPND    HMDB0037809
HETATM    1  C1  UNL     1      -2.519  -1.785  -0.271  1.00  0.00           C  
HETATM    2  C2  UNL     1      -2.326  -0.490   0.476  1.00  0.00           C  
HETATM    3  O1  UNL     1      -3.424   0.341   0.435  1.00  0.00           O  
HETATM    4  C3  UNL     1      -3.159   1.404  -0.389  1.00  0.00           C  
HETATM    5  C4  UNL     1      -1.643   1.616  -0.375  1.00  0.00           C  
HETATM    6  C5  UNL     1      -1.150   0.294   0.061  1.00  0.00           C  
HETATM    7  S1  UNL     1       0.140   0.406   1.366  1.00  0.00           S  
HETATM    8  C6  UNL     1       1.318  -0.751   0.730  1.00  0.00           C  
HETATM    9  C7  UNL     1       2.710  -0.677   1.154  1.00  0.00           C  
HETATM   10  C8  UNL     1       3.457  -0.765  -0.189  1.00  0.00           C  
HETATM   11  O2  UNL     1       2.451  -1.014  -1.158  1.00  0.00           O  
HETATM   12  C9  UNL     1       1.450  -0.219  -0.716  1.00  0.00           C  
HETATM   13  C10 UNL     1       1.820   1.239  -0.591  1.00  0.00           C  
HETATM   14  S2  UNL     1      -0.197  -0.501  -1.295  1.00  0.00           S  
HETATM   15  H1  UNL     1      -2.718  -1.666  -1.335  1.00  0.00           H  
HETATM   16  H2  UNL     1      -3.348  -2.346   0.228  1.00  0.00           H  
HETATM   17  H3  UNL     1      -1.601  -2.401  -0.065  1.00  0.00           H  
HETATM   18  H4  UNL     1      -2.188  -0.778   1.560  1.00  0.00           H  
HETATM   19  H5  UNL     1      -3.660   2.338  -0.098  1.00  0.00           H  
HETATM   20  H6  UNL     1      -3.484   1.109  -1.428  1.00  0.00           H  
HETATM   21  H7  UNL     1      -1.357   2.411   0.339  1.00  0.00           H  
HETATM   22  H8  UNL     1      -1.360   1.865  -1.419  1.00  0.00           H  
HETATM   23  H9  UNL     1       0.889  -1.771   0.701  1.00  0.00           H  
HETATM   24  H10 UNL     1       3.031   0.160   1.757  1.00  0.00           H  
HETATM   25  H11 UNL     1       2.981  -1.621   1.705  1.00  0.00           H  
HETATM   26  H12 UNL     1       4.199  -1.564  -0.192  1.00  0.00           H  
HETATM   27  H13 UNL     1       3.870   0.234  -0.441  1.00  0.00           H  
HETATM   28  H14 UNL     1       2.536   1.543  -1.398  1.00  0.00           H  
HETATM   29  H15 UNL     1       2.331   1.478   0.362  1.00  0.00           H  
HETATM   30  H16 UNL     1       0.950   1.910  -0.670  1.00  0.00           H  
CONECT    1    2   15   16   17
CONECT    2    3    6   18
CONECT    3    4
CONECT    4    5   19   20
CONECT    5    6   21   22
CONECT    6    7   14
CONECT    7    8
CONECT    8    9   12   23
CONECT    9   10   24   25
CONECT   10   11   26   27
CONECT   11   12
CONECT   12   13   14
CONECT   13   28   29   30
END

HMDB0037809
     RDKit          3D
Hexahydro-2',3alpha-dimethylspiro[1,3-dithiolo[4,5-b]furan-2,3'(2'H)-furan]
 30 32  0  0  0  0  0  0  0  0999 V2000
   -2.5190   -1.7845   -0.2707 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3261   -0.4902    0.4762 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4241    0.3406    0.4353 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1585    1.4045   -0.3891 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6431    1.6163   -0.3755 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1502    0.2944    0.0610 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1398    0.4059    1.3661 S   0  0  0  0  0  0  0  0  0  0  0  0
    1.3177   -0.7506    0.7300 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7099   -0.6774    1.1542 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4565   -0.7650   -0.1886 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4509   -1.0144   -1.1581 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4497   -0.2192   -0.7160 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8198    1.2389   -0.5912 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1968   -0.5012   -1.2955 S   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7179   -1.6656   -1.3352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3476   -2.3460    0.2276 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6009   -2.4013   -0.0654 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1879   -0.7776    1.5600 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6604    2.3380   -0.0976 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4840    1.1093   -1.4276 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3571    2.4111    0.3388 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3599    1.8648   -1.4194 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8893   -1.7707    0.7012 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0309    0.1598    1.7565 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9810   -1.6207    1.7052 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1992   -1.5635   -0.1924 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8705    0.2344   -0.4408 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5365    1.5427   -1.3976 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3313    1.4776    0.3623 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9504    1.9096   -0.6696 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  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
 11 12  1  0
 12 13  1  0
 12 14  1  0
  6  2  1  0
 12  8  1  0
 14  6  1  0
  1 15  1  0
  1 16  1  0
  1 17  1  0
  2 18  1  0
  4 19  1  0
  4 20  1  0
  5 21  1  0
  5 22  1  0
  8 23  1  0
  9 24  1  0
  9 25  1  0
 10 26  1  0
 10 27  1  0
 13 28  1  0
 13 29  1  0
 13 30  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
Hexahydro-2',3a-dimethylspiro[1,3-dithiolo[4,5-b]furan-2,3'(2'H)-furan]	Generator
Hexahydro-2',3α-dimethylspiro[1,3-dithiolo[4,5-b]furan-2,3'(2'H)-furan]	Generator

Chemical Formula

C₁₀H₁₆O₂S₂

Average Molecular Weight

232.363

Monoisotopic Molecular Weight

232.059171136

IUPAC Name

2',3a-dimethyl-tetrahydrospiro[[1,3]dithiolo[4,5-b]furan-2,3'-oxolane]

Traditional Name

2',3a-dimethyl-dihydro-5H-spiro[[1,3]dithiolo[4,5-b]furan-2,3'-oxolane]

CAS Registry Number

38325-25-6

SMILES

CC1OCCC11SC2CCOC2(C)S1

InChI Identifier

InChI=1S/C10H16O2S2/c1-7-10(4-6-11-7)13-8-3-5-12-9(8,2)14-10/h7-8H,3-6H2,1-2H3

InChI Key

LGPJANFPSFABDB-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as monothioketals. Monothioketals are compounds containing a monothioketal functional group with the general structure R2C(OR')(SR') with (R = any atom but H).

Kingdom

Organic compounds

Super Class

Organosulfur compounds

Class

Thioacetals

Sub Class

Monothioacetals

Direct Parent

Monothioketals

Alternative Parents

Substituents

Dithioketal
Monothioketal
Thioacetal
Dithiolane
Tetrahydrofuran
1,3-dithiolane
Thioether
Ether
Dialkyl ether
Dialkylthioether
Organoheterocyclic compound
Oxacycle
Organooxygen compound
Hydrocarbon derivative
Organic oxygen compound
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Organoleptic effect

Odor

meaty

Disposition

Biological location

Cellular substructure

Extracellular (HMDB: HMDB0037809)
Cytoplasm (HMDB: HMDB0037809)

Source

Exogenous

Food

Food (HMDB: HMDB0037809)

Not Available

Nutrient (HMDB: HMDB0037809)

Physical Properties

State

Not Available

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	135.00 to 140.00 °C. @ 3.00 mm Hg	The Good Scents Company Information System
Water Solubility	68.67 mg/L @ 25 °C (est)	The Good Scents Company Information System
LogP	2.832 (est)	The Good Scents Company Information System

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.18 g/L	ALOGPS
logP	2.09	ALOGPS
logP	2.27	ChemAxon
logS	-3.1	ALOGPS
pKa (Strongest Basic)	-3.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	18.46 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	60.68 m³·mol⁻¹	ChemAxon
Polarizability	24.28 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	152.611	31661259
DarkChem	[M-H]-	146.742	31661259
DeepCCS	[M-2H]-	181.603	30932474
DeepCCS	[M+Na]+	157.127	30932474
AllCCS	[M+H]+	150.7	32859911
AllCCS	[M+H-H2O]+	147.1	32859911
AllCCS	[M+NH4]+	154.1	32859911
AllCCS	[M+Na]+	155.1	32859911
AllCCS	[M-H]-	153.4	32859911
AllCCS	[M+Na-2H]-	153.8	32859911
AllCCS	[M+HCOO]-	154.4	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Hexahydro-2',3alpha-dimethylspiro[1,3-dithiolo[4,5-b]furan-2,3'(2'H)-furan]	CC1OCCC11SC2CCOC2(C)S1	2319.2	Standard polar	33892256
Hexahydro-2',3alpha-dimethylspiro[1,3-dithiolo[4,5-b]furan-2,3'(2'H)-furan]	CC1OCCC11SC2CCOC2(C)S1	1625.4	Standard non polar	33892256
Hexahydro-2',3alpha-dimethylspiro[1,3-dithiolo[4,5-b]furan-2,3'(2'H)-furan]	CC1OCCC11SC2CCOC2(C)S1	1717.8	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 - Hexahydro-2',3alpha-dimethylspiro[1,3-dithiolo[4,5-b]furan-2,3'(2'H)-furan] GC-MS (Non-derivatized) - 70eV, Positive	splash10-0gb9-4950000000-24c75a1a478e3bb543cd	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Hexahydro-2',3alpha-dimethylspiro[1,3-dithiolo[4,5-b]furan-2,3'(2'H)-furan] 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 - Hexahydro-2',3alpha-dimethylspiro[1,3-dithiolo[4,5-b]furan-2,3'(2'H)-furan] 10V, Positive-QTOF	splash10-0aor-9520000000-f20d385507da45a44fc1	2016-06-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Hexahydro-2',3alpha-dimethylspiro[1,3-dithiolo[4,5-b]furan-2,3'(2'H)-furan] 20V, Positive-QTOF	splash10-014i-2940000000-d70e0b612622d9e89b4d	2016-06-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Hexahydro-2',3alpha-dimethylspiro[1,3-dithiolo[4,5-b]furan-2,3'(2'H)-furan] 40V, Positive-QTOF	splash10-0a4i-9000000000-5570274e78a958ad689d	2016-06-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Hexahydro-2',3alpha-dimethylspiro[1,3-dithiolo[4,5-b]furan-2,3'(2'H)-furan] 10V, Negative-QTOF	splash10-001i-1490000000-97e1902f5fb8e8c83f29	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Hexahydro-2',3alpha-dimethylspiro[1,3-dithiolo[4,5-b]furan-2,3'(2'H)-furan] 20V, Negative-QTOF	splash10-0159-7900000000-489273e89c8a851ab99d	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Hexahydro-2',3alpha-dimethylspiro[1,3-dithiolo[4,5-b]furan-2,3'(2'H)-furan] 40V, Negative-QTOF	splash10-0bti-9200000000-194b520a557ebaad7b94	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Hexahydro-2',3alpha-dimethylspiro[1,3-dithiolo[4,5-b]furan-2,3'(2'H)-furan] 10V, Negative-QTOF	splash10-001i-0090000000-6b9b34f3eb47fc4dd934	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Hexahydro-2',3alpha-dimethylspiro[1,3-dithiolo[4,5-b]furan-2,3'(2'H)-furan] 20V, Negative-QTOF	splash10-00lr-0690000000-63469d1556d50a188aa1	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Hexahydro-2',3alpha-dimethylspiro[1,3-dithiolo[4,5-b]furan-2,3'(2'H)-furan] 40V, Negative-QTOF	splash10-001i-7940000000-d7304c149ca21e72016e	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Hexahydro-2',3alpha-dimethylspiro[1,3-dithiolo[4,5-b]furan-2,3'(2'H)-furan] 10V, Positive-QTOF	splash10-001i-0090000000-81f5c7c17e5ce456eac4	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Hexahydro-2',3alpha-dimethylspiro[1,3-dithiolo[4,5-b]furan-2,3'(2'H)-furan] 20V, Positive-QTOF	splash10-0159-2950000000-3446d44b25b07dcdd724	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Hexahydro-2',3alpha-dimethylspiro[1,3-dithiolo[4,5-b]furan-2,3'(2'H)-furan] 40V, Positive-QTOF	splash10-0avr-9740000000-11f221b89b48c6b4d613	2021-09-24	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Cytoplasm
Extracellular

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

FDB016954

KNApSAcK ID

Not Available

Chemspider ID

55830

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

61979

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

rw1035731

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

(). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .

Showing metabocard for Hexahydro-2',3alpha-dimethylspiro[1,3-dithiolo[4,5-b]furan-2,3'(2'H)-furan] (HMDB0037809)

MOL for HMDB0037809 (Hexahydro-2',3alpha-dimethylspiro[1,3-dithiolo[4,5-b]furan-2,3'(2'H)-furan])

3D MOL for HMDB0037809 (Hexahydro-2',3alpha-dimethylspiro[1,3-dithiolo[4,5-b]furan-2,3'(2'H)-furan])

3D SDF for HMDB0037809 (Hexahydro-2',3alpha-dimethylspiro[1,3-dithiolo[4,5-b]furan-2,3'(2'H)-furan])

3D-SDF for HMDB0037809 (Hexahydro-2',3alpha-dimethylspiro[1,3-dithiolo[4,5-b]furan-2,3'(2'H)-furan])

PDB for HMDB0037809 (Hexahydro-2',3alpha-dimethylspiro[1,3-dithiolo[4,5-b]furan-2,3'(2'H)-furan])

3D PDB for HMDB0037809 (Hexahydro-2',3alpha-dimethylspiro[1,3-dithiolo[4,5-b]furan-2,3'(2'H)-furan])

SMILES for HMDB0037809 (Hexahydro-2',3alpha-dimethylspiro[1,3-dithiolo[4,5-b]furan-2,3'(2'H)-furan])

INCHI for HMDB0037809 (Hexahydro-2',3alpha-dimethylspiro[1,3-dithiolo[4,5-b]furan-2,3'(2'H)-furan])

Structure for HMDB0037809 (Hexahydro-2',3alpha-dimethylspiro[1,3-dithiolo[4,5-b]furan-2,3'(2'H)-furan])

3D Structure for HMDB0037809 (Hexahydro-2',3alpha-dimethylspiro[1,3-dithiolo[4,5-b]furan-2,3'(2'H)-furan])

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

GC-MS Spectra

MS/MS Spectra