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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 20:34:39 UTC

Update Date

2022-03-07 02:54:33 UTC

HMDB ID

HMDB0035569

Secondary Accession Numbers

HMDB35569

Metabolite Identification

Common Name

4,6-Docosanedione

Description

4,6-Docosanedione belongs to the class of organic compounds known as beta-diketones. These are organic compounds containing two keto groups separated by a single carbon atom. 4,6-Docosanedione has been detected, but not quantified in, fats and oils. This could make 4,6-docosanedione a potential biomarker for the consumption of these foods. Based on a literature review a significant number of articles have been published on 4,6-Docosanedione.

Structure

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

HMDB0035569
     RDKit          3D
4,6-Docosanedione
 66 65  0  0  0  0  0  0  0  0999 V2000
    6.2198    2.6185   -1.3138 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0377    2.2182   -2.7217 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4785    0.8889   -3.0360 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1404    0.5281   -2.5629 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8364    0.4442   -1.1316 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5898   -0.5571   -0.3344 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3708   -1.9325   -0.8455 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9038   -2.3020   -0.7994 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3193   -2.2536    0.5808 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8760   -2.6810    0.5597 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0574   -1.7660   -0.2882 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3864   -2.2113   -0.2769 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9118   -2.1589    1.1388 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3787   -2.5930    1.0488 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9675   -2.5741    2.4199 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9027   -1.2078    3.0147 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6408   -0.1807    2.2226 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2621   -0.3826    1.2157 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5930    1.2306    2.7450 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3608    2.1139    1.8538 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5637    2.1471    1.9740 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6593    2.9515    0.8215 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7080    3.7352    0.0735 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9980    4.5837   -0.9677 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3802    3.2616   -0.9612 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0984    3.3468   -1.2890 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5216    1.8335   -0.6173 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0586    2.2619   -3.2221 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4902    3.0564   -3.2465 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2585    0.0899   -2.8440 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4242    0.8578   -4.1731 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4081    1.2209   -3.0491 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8806   -0.4714   -3.0307 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9291    1.4406   -0.5902 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7507    0.2271   -1.0153 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6738   -0.3094   -0.2161 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2094   -0.5148    0.7194 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9447   -2.7112   -0.2903 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6650   -1.9812   -1.9177 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3062   -1.6428   -1.4623 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7488   -3.3291   -1.2455 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.2469    4.4325    0.7333 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4077    3.0043   -0.3885 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.7081    5.3313   -1.3332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6468    3.8773   -1.7590 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
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 24 66  1  0
M  END


  Mrv0541 05061308332D          

 24 23  0  0  0  0            999 V2000
  -10.0914    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9124    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3770    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1980    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6625    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9480    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2336    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5191    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8046    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0901    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3757    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6612    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9467    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2323    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5178    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8033    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0888    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4835    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6256    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0546    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7690    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3401    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7690    4.1763    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3401    4.1763    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  3  1  1  0  0  0  0
  4  2  1  0  0  0  0
  5  3  1  0  0  0  0
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 10  9  1  0  0  0  0
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 18  4  1  0  0  0  0
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 23 21  2  0  0  0  0
 24 22  2  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0035569

> <DATABASE_NAME>
hmdb

> <SMILES>
CCCCCCCCCCCCCCCCC(=O)CC(=O)CCC

> <INCHI_IDENTIFIER>
InChI=1S/C22H42O2/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17-19-22(24)20-21(23)18-4-2/h3-20H2,1-2H3

> <INCHI_KEY>
WQFAWBQWACWQMD-UHFFFAOYSA-N

> <FORMULA>
C22H42O2

> <MOLECULAR_WEIGHT>
338.5677

> <EXACT_MASS>
338.318480588

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_AVERAGE_POLARIZABILITY>
45.42953647927559

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
docosane-4,6-dione

> <ALOGPS_LOGP>
8.02

> <JCHEM_LOGP>
8.397735446

> <ALOGPS_LOGS>
-6.80

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.812658826134702

> <JCHEM_PKA_STRONGEST_BASIC>
-7.189081185467565

> <JCHEM_POLAR_SURFACE_AREA>
34.14

> <JCHEM_REFRACTIVITY>
104.35879999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
19

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.41e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
docosane-4,6-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0035569
     RDKit          3D
4,6-Docosanedione
 66 65  0  0  0  0  0  0  0  0999 V2000
    6.2198    2.6185   -1.3138 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0377    2.2182   -2.7217 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4785    0.8889   -3.0360 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1404    0.5281   -2.5629 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8364    0.4442   -1.1316 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5898   -0.5571   -0.3344 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3708   -1.9325   -0.8455 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.5637    2.1471    1.9740 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6593    2.9515    0.8215 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.9980    4.5837   -0.9677 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3802    3.2616   -0.9612 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.0499   -0.7552    0.2187 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4085   -3.2664   -0.6638 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9801   -1.6161   -0.9732 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4503   -2.8903    1.8176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7891   -1.1545    1.5514 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3898   -3.6490    0.6392 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9115   -2.0017    0.2900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0093   -2.9639    2.3560 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3977   -3.3233    3.0244 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8800   -0.8310    3.1870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4301   -1.2894    4.0207 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5384    1.6002    2.7976 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9561    1.2416    3.7925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9328    3.6298    1.3331 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0710    2.3033    0.1528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2469    4.4325    0.7333 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4077    3.0043   -0.3885 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1306    5.0450   -0.4586 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7081    5.3313   -1.3332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6468    3.8773   -1.7590 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
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 17 19  1  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
 22 23  1  0
 23 24  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  2 28  1  0
  2 29  1  0
  3 30  1  0
  3 31  1  0
  4 32  1  0
  4 33  1  0
  5 34  1  0
  5 35  1  0
  6 36  1  0
  6 37  1  0
  7 38  1  0
  7 39  1  0
  8 40  1  0
  8 41  1  0
  9 42  1  0
  9 43  1  0
 10 44  1  0
 10 45  1  0
 11 46  1  0
 11 47  1  0
 12 48  1  0
 12 49  1  0
 13 50  1  0
 13 51  1  0
 14 52  1  0
 14 53  1  0
 15 54  1  0
 15 55  1  0
 16 56  1  0
 16 57  1  0
 19 58  1  0
 19 59  1  0
 22 60  1  0
 22 61  1  0
 23 62  1  0
 23 63  1  0
 24 64  1  0
 24 65  1  0
 24 66  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     -18.837   9.336   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.170  10.106   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -17.504  10.106   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.836   9.336   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0     -16.170   9.336   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0     -14.836  10.106   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0     -13.503   9.336   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0     -12.169  10.106   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0     -10.835   9.336   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -9.502  10.106   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -8.168   9.336   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -6.834  10.106   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -5.501   9.336   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -4.167  10.106   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.833   9.336   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.499  10.106   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.166   9.336   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.503  10.106   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.168  10.106   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.835  10.106   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.169   9.336   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.502   9.336   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       5.169   7.796   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       2.502   7.796   0.000  0.00  0.00           O+0
CONECT    1    3                                                            
CONECT    2    4                                                            
CONECT    3    1    5                                                       
CONECT    4    2   18                                                       
CONECT    5    3    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   19                                                       
CONECT   18    4   21                                                       
CONECT   19   17   22                                                       
CONECT   20   21   22                                                       
CONECT   21   18   20   23                                                  
CONECT   22   19   20   24                                                  
CONECT   23   21                                                            
CONECT   24   22                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   46    0
END

COMPND    HMDB0035569
HETATM    1  C1  UNL     1       6.220   2.619  -1.314  1.00  0.00           C  
HETATM    2  C2  UNL     1       6.038   2.218  -2.722  1.00  0.00           C  
HETATM    3  C3  UNL     1       5.478   0.889  -3.036  1.00  0.00           C  
HETATM    4  C4  UNL     1       4.140   0.528  -2.563  1.00  0.00           C  
HETATM    5  C5  UNL     1       3.836   0.444  -1.132  1.00  0.00           C  
HETATM    6  C6  UNL     1       4.590  -0.557  -0.334  1.00  0.00           C  
HETATM    7  C7  UNL     1       4.371  -1.932  -0.846  1.00  0.00           C  
HETATM    8  C8  UNL     1       2.904  -2.302  -0.799  1.00  0.00           C  
HETATM    9  C9  UNL     1       2.319  -2.254   0.581  1.00  0.00           C  
HETATM   10  C10 UNL     1       0.876  -2.681   0.560  1.00  0.00           C  
HETATM   11  C11 UNL     1       0.057  -1.766  -0.288  1.00  0.00           C  
HETATM   12  C12 UNL     1      -1.386  -2.211  -0.277  1.00  0.00           C  
HETATM   13  C13 UNL     1      -1.912  -2.159   1.139  1.00  0.00           C  
HETATM   14  C14 UNL     1      -3.379  -2.593   1.049  1.00  0.00           C  
HETATM   15  C15 UNL     1      -3.967  -2.574   2.420  1.00  0.00           C  
HETATM   16  C16 UNL     1      -3.903  -1.208   3.015  1.00  0.00           C  
HETATM   17  C17 UNL     1      -4.641  -0.181   2.223  1.00  0.00           C  
HETATM   18  O1  UNL     1      -5.262  -0.383   1.216  1.00  0.00           O  
HETATM   19  C18 UNL     1      -4.593   1.231   2.745  1.00  0.00           C  
HETATM   20  C19 UNL     1      -5.361   2.114   1.854  1.00  0.00           C  
HETATM   21  O2  UNL     1      -6.564   2.147   1.974  1.00  0.00           O  
HETATM   22  C20 UNL     1      -4.659   2.951   0.822  1.00  0.00           C  
HETATM   23  C21 UNL     1      -5.708   3.735   0.073  1.00  0.00           C  
HETATM   24  C22 UNL     1      -4.998   4.584  -0.968  1.00  0.00           C  
HETATM   25  H1  UNL     1       5.380   3.262  -0.961  1.00  0.00           H  
HETATM   26  H2  UNL     1       7.098   3.347  -1.289  1.00  0.00           H  
HETATM   27  H3  UNL     1       6.522   1.834  -0.617  1.00  0.00           H  
HETATM   28  H4  UNL     1       7.059   2.262  -3.222  1.00  0.00           H  
HETATM   29  H5  UNL     1       5.490   3.056  -3.246  1.00  0.00           H  
HETATM   30  H6  UNL     1       6.259   0.090  -2.844  1.00  0.00           H  
HETATM   31  H7  UNL     1       5.424   0.858  -4.173  1.00  0.00           H  
HETATM   32  H8  UNL     1       3.408   1.221  -3.049  1.00  0.00           H  
HETATM   33  H9  UNL     1       3.881  -0.471  -3.031  1.00  0.00           H  
HETATM   34  H10 UNL     1       3.929   1.441  -0.590  1.00  0.00           H  
HETATM   35  H11 UNL     1       2.751   0.227  -1.015  1.00  0.00           H  
HETATM   36  H12 UNL     1       5.674  -0.309  -0.216  1.00  0.00           H  
HETATM   37  H13 UNL     1       4.209  -0.515   0.719  1.00  0.00           H  
HETATM   38  H14 UNL     1       4.945  -2.711  -0.290  1.00  0.00           H  
HETATM   39  H15 UNL     1       4.665  -1.981  -1.918  1.00  0.00           H  
HETATM   40  H16 UNL     1       2.306  -1.643  -1.462  1.00  0.00           H  
HETATM   41  H17 UNL     1       2.749  -3.329  -1.245  1.00  0.00           H  
HETATM   42  H18 UNL     1       2.390  -1.207   0.999  1.00  0.00           H  
HETATM   43  H19 UNL     1       2.918  -2.858   1.304  1.00  0.00           H  
HETATM   44  H20 UNL     1       0.775  -3.727   0.146  1.00  0.00           H  
HETATM   45  H21 UNL     1       0.482  -2.774   1.599  1.00  0.00           H  
HETATM   46  H22 UNL     1       0.424  -1.648  -1.327  1.00  0.00           H  
HETATM   47  H23 UNL     1       0.050  -0.755   0.219  1.00  0.00           H  
HETATM   48  H24 UNL     1      -1.409  -3.266  -0.664  1.00  0.00           H  
HETATM   49  H25 UNL     1      -1.980  -1.616  -0.973  1.00  0.00           H  
HETATM   50  H26 UNL     1      -1.450  -2.890   1.818  1.00  0.00           H  
HETATM   51  H27 UNL     1      -1.789  -1.155   1.551  1.00  0.00           H  
HETATM   52  H28 UNL     1      -3.390  -3.649   0.639  1.00  0.00           H  
HETATM   53  H29 UNL     1      -3.911  -2.002   0.290  1.00  0.00           H  
HETATM   54  H30 UNL     1      -5.009  -2.964   2.356  1.00  0.00           H  
HETATM   55  H31 UNL     1      -3.398  -3.323   3.024  1.00  0.00           H  
HETATM   56  H32 UNL     1      -2.880  -0.831   3.187  1.00  0.00           H  
HETATM   57  H33 UNL     1      -4.430  -1.289   4.021  1.00  0.00           H  
HETATM   58  H34 UNL     1      -3.538   1.600   2.798  1.00  0.00           H  
HETATM   59  H35 UNL     1      -4.956   1.242   3.793  1.00  0.00           H  
HETATM   60  H36 UNL     1      -3.933   3.630   1.333  1.00  0.00           H  
HETATM   61  H37 UNL     1      -4.071   2.303   0.153  1.00  0.00           H  
HETATM   62  H38 UNL     1      -6.247   4.433   0.733  1.00  0.00           H  
HETATM   63  H39 UNL     1      -6.408   3.004  -0.388  1.00  0.00           H  
HETATM   64  H40 UNL     1      -4.131   5.045  -0.459  1.00  0.00           H  
HETATM   65  H41 UNL     1      -5.708   5.331  -1.333  1.00  0.00           H  
HETATM   66  H42 UNL     1      -4.647   3.877  -1.759  1.00  0.00           H  
CONECT    1    2   25   26   27
CONECT    2    3   28   29
CONECT    3    4   30   31
CONECT    4    5   32   33
CONECT    5    6   34   35
CONECT    6    7   36   37
CONECT    7    8   38   39
CONECT    8    9   40   41
CONECT    9   10   42   43
CONECT   10   11   44   45
CONECT   11   12   46   47
CONECT   12   13   48   49
CONECT   13   14   50   51
CONECT   14   15   52   53
CONECT   15   16   54   55
CONECT   16   17   56   57
CONECT   17   18   18   19
CONECT   19   20   58   59
CONECT   20   21   21   22
CONECT   22   23   60   61
CONECT   23   24   62   63
CONECT   24   64   65   66
END

HMDB0035569
     RDKit          3D
4,6-Docosanedione
 66 65  0  0  0  0  0  0  0  0999 V2000
    6.2198    2.6185   -1.3138 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0377    2.2182   -2.7217 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4785    0.8889   -3.0360 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1404    0.5281   -2.5629 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8364    0.4442   -1.1316 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5898   -0.5571   -0.3344 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3708   -1.9325   -0.8455 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9038   -2.3020   -0.7994 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3193   -2.2536    0.5808 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8760   -2.6810    0.5597 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0574   -1.7660   -0.2882 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3864   -2.2113   -0.2769 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9118   -2.1589    1.1388 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3787   -2.5930    1.0488 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9675   -2.5741    2.4199 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9027   -1.2078    3.0147 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6408   -0.1807    2.2226 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2621   -0.3826    1.2157 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5930    1.2306    2.7450 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3608    2.1139    1.8538 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5637    2.1471    1.9740 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6593    2.9515    0.8215 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7080    3.7352    0.0735 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9980    4.5837   -0.9677 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3802    3.2616   -0.9612 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0984    3.3468   -1.2890 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5216    1.8335   -0.6173 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0586    2.2619   -3.2221 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4902    3.0564   -3.2465 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2585    0.0899   -2.8440 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4242    0.8578   -4.1731 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4081    1.2209   -3.0491 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8806   -0.4714   -3.0307 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9291    1.4406   -0.5902 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7507    0.2271   -1.0153 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6738   -0.3094   -0.2161 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2094   -0.5148    0.7194 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9447   -2.7112   -0.2903 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6650   -1.9812   -1.9177 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3062   -1.6428   -1.4623 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7488   -3.3291   -1.2455 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3895   -1.2070    0.9989 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9183   -2.8582    1.3042 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7754   -3.7272    0.1465 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4821   -2.7743    1.5992 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4242   -1.6478   -1.3266 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0499   -0.7552    0.2187 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4085   -3.2664   -0.6638 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9801   -1.6161   -0.9732 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4503   -2.8903    1.8176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7891   -1.1545    1.5514 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3898   -3.6490    0.6392 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9115   -2.0017    0.2900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0093   -2.9639    2.3560 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3977   -3.3233    3.0244 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8800   -0.8310    3.1870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4301   -1.2894    4.0207 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5384    1.6002    2.7976 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9561    1.2416    3.7925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9328    3.6298    1.3331 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0710    2.3033    0.1528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2469    4.4325    0.7333 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4077    3.0043   -0.3885 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1306    5.0450   -0.4586 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7081    5.3313   -1.3332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6468    3.8773   -1.7590 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
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 17 19  1  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
 22 23  1  0
 23 24  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  2 28  1  0
  2 29  1  0
  3 30  1  0
  3 31  1  0
  4 32  1  0
  4 33  1  0
  5 34  1  0
  5 35  1  0
  6 36  1  0
  6 37  1  0
  7 38  1  0
  7 39  1  0
  8 40  1  0
  8 41  1  0
  9 42  1  0
  9 43  1  0
 10 44  1  0
 10 45  1  0
 11 46  1  0
 11 47  1  0
 12 48  1  0
 12 49  1  0
 13 50  1  0
 13 51  1  0
 14 52  1  0
 14 53  1  0
 15 54  1  0
 15 55  1  0
 16 56  1  0
 16 57  1  0
 19 58  1  0
 19 59  1  0
 22 60  1  0
 22 61  1  0
 23 62  1  0
 23 63  1  0
 24 64  1  0
 24 65  1  0
 24 66  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₂₂H₄₂O₂

Average Molecular Weight

338.5677

Monoisotopic Molecular Weight

338.318480588

IUPAC Name

docosane-4,6-dione

Traditional Name

docosane-4,6-dione

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCCCCCCC(=O)CC(=O)CCC

InChI Identifier

InChI=1S/C22H42O2/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17-19-22(24)20-21(23)18-4-2/h3-20H2,1-2H3

InChI Key

WQFAWBQWACWQMD-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as beta-diketones. These are organic compounds containing two keto groups separated by a single carbon atom.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbonyl compounds

Direct Parent

Beta-diketones

Alternative Parents

Substituents

1,3-diketone
Ketone
Organic oxide
Hydrocarbon derivative
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cell membrane (HMDB: HMDB0035569)

Cellular substructure

Membrane (HMDB: HMDB0035569)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0035569)

Source

Exogenous

Food

Food (HMDB: HMDB0035569)

Fat and oil

Fats and oils (FooDB: FOOD00864)

Not Available

Nutrient (HMDB: HMDB0035569)

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	5.4e-05 g/L	ALOGPS
logP	8.02	ALOGPS
logP	8.4	ChemAxon
logS	-6.8	ALOGPS
pKa (Strongest Acidic)	7.81	ChemAxon
pKa (Strongest Basic)	-7.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	34.14 Å²	ChemAxon
Rotatable Bond Count	19	ChemAxon
Refractivity	104.36 m³·mol⁻¹	ChemAxon
Polarizability	45.43 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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
DeepCCS	[M+H]+	191.738	30932474
DeepCCS	[M-H]-	189.188	30932474
DeepCCS	[M-2H]-	222.391	30932474
DeepCCS	[M+Na]+	198.613	30932474
AllCCS	[M+H]+	201.7	32859911
AllCCS	[M+H-H2O]+	199.2	32859911
AllCCS	[M+NH4]+	204.1	32859911
AllCCS	[M+Na]+	204.8	32859911
AllCCS	[M-H]-	192.7	32859911
AllCCS	[M+Na-2H]-	194.7	32859911
AllCCS	[M+HCOO]-	197.1	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
4,6-Docosanedione	CCCCCCCCCCCCCCCCC(=O)CC(=O)CCC	2966.0	Standard polar	33892256
4,6-Docosanedione	CCCCCCCCCCCCCCCCC(=O)CC(=O)CCC	2445.7	Standard non polar	33892256
4,6-Docosanedione	CCCCCCCCCCCCCCCCC(=O)CC(=O)CCC	2479.1	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
4,6-Docosanedione,1TMS,isomer #1	CCCCCCCCCCCCCCCCC(=CC(=O)CCC)O[Si](C)(C)C	2640.1	Semi standard non polar	33892256
4,6-Docosanedione,1TMS,isomer #1	CCCCCCCCCCCCCCCCC(=CC(=O)CCC)O[Si](C)(C)C	2565.0	Standard non polar	33892256
4,6-Docosanedione,1TMS,isomer #2	CCCCCCCCCCCCCCCC=C(CC(=O)CCC)O[Si](C)(C)C	2632.6	Semi standard non polar	33892256
4,6-Docosanedione,1TMS,isomer #2	CCCCCCCCCCCCCCCC=C(CC(=O)CCC)O[Si](C)(C)C	2584.9	Standard non polar	33892256
4,6-Docosanedione,1TMS,isomer #3	CCC=C(CC(=O)CCCCCCCCCCCCCCCC)O[Si](C)(C)C	2634.2	Semi standard non polar	33892256
4,6-Docosanedione,1TMS,isomer #3	CCC=C(CC(=O)CCCCCCCCCCCCCCCC)O[Si](C)(C)C	2611.4	Standard non polar	33892256
4,6-Docosanedione,1TMS,isomer #4	CCCCCCCCCCCCCCCCC(=O)C=C(CCC)O[Si](C)(C)C	2638.9	Semi standard non polar	33892256
4,6-Docosanedione,1TMS,isomer #4	CCCCCCCCCCCCCCCCC(=O)C=C(CCC)O[Si](C)(C)C	2567.9	Standard non polar	33892256
4,6-Docosanedione,2TMS,isomer #1	CCC=C(C=C(CCCCCCCCCCCCCCCC)O[Si](C)(C)C)O[Si](C)(C)C	2753.8	Semi standard non polar	33892256
4,6-Docosanedione,2TMS,isomer #1	CCC=C(C=C(CCCCCCCCCCCCCCCC)O[Si](C)(C)C)O[Si](C)(C)C	2692.2	Standard non polar	33892256
4,6-Docosanedione,2TMS,isomer #2	CCC=C(CC(=CCCCCCCCCCCCCCCC)O[Si](C)(C)C)O[Si](C)(C)C	2738.6	Semi standard non polar	33892256
4,6-Docosanedione,2TMS,isomer #2	CCC=C(CC(=CCCCCCCCCCCCCCCC)O[Si](C)(C)C)O[Si](C)(C)C	2694.5	Standard non polar	33892256
4,6-Docosanedione,2TMS,isomer #3	CCCCCCCCCCCCCCCC=C(C=C(CCC)O[Si](C)(C)C)O[Si](C)(C)C	2740.6	Semi standard non polar	33892256
4,6-Docosanedione,2TMS,isomer #3	CCCCCCCCCCCCCCCC=C(C=C(CCC)O[Si](C)(C)C)O[Si](C)(C)C	2663.8	Standard non polar	33892256
4,6-Docosanedione,1TBDMS,isomer #1	CCCCCCCCCCCCCCCCC(=CC(=O)CCC)O[Si](C)(C)C(C)(C)C	2906.4	Semi standard non polar	33892256
4,6-Docosanedione,1TBDMS,isomer #1	CCCCCCCCCCCCCCCCC(=CC(=O)CCC)O[Si](C)(C)C(C)(C)C	2723.0	Standard non polar	33892256
4,6-Docosanedione,1TBDMS,isomer #2	CCCCCCCCCCCCCCCC=C(CC(=O)CCC)O[Si](C)(C)C(C)(C)C	2884.0	Semi standard non polar	33892256
4,6-Docosanedione,1TBDMS,isomer #2	CCCCCCCCCCCCCCCC=C(CC(=O)CCC)O[Si](C)(C)C(C)(C)C	2714.7	Standard non polar	33892256
4,6-Docosanedione,1TBDMS,isomer #3	CCC=C(CC(=O)CCCCCCCCCCCCCCCC)O[Si](C)(C)C(C)(C)C	2878.0	Semi standard non polar	33892256
4,6-Docosanedione,1TBDMS,isomer #3	CCC=C(CC(=O)CCCCCCCCCCCCCCCC)O[Si](C)(C)C(C)(C)C	2755.1	Standard non polar	33892256
4,6-Docosanedione,1TBDMS,isomer #4	CCCCCCCCCCCCCCCCC(=O)C=C(CCC)O[Si](C)(C)C(C)(C)C	2906.3	Semi standard non polar	33892256
4,6-Docosanedione,1TBDMS,isomer #4	CCCCCCCCCCCCCCCCC(=O)C=C(CCC)O[Si](C)(C)C(C)(C)C	2722.9	Standard non polar	33892256
4,6-Docosanedione,2TBDMS,isomer #1	CCC=C(C=C(CCCCCCCCCCCCCCCC)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3278.6	Semi standard non polar	33892256
4,6-Docosanedione,2TBDMS,isomer #1	CCC=C(C=C(CCCCCCCCCCCCCCCC)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3004.8	Standard non polar	33892256
4,6-Docosanedione,2TBDMS,isomer #2	CCC=C(CC(=CCCCCCCCCCCCCCCC)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3217.9	Semi standard non polar	33892256
4,6-Docosanedione,2TBDMS,isomer #2	CCC=C(CC(=CCCCCCCCCCCCCCCC)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3013.5	Standard non polar	33892256
4,6-Docosanedione,2TBDMS,isomer #3	CCCCCCCCCCCCCCCC=C(C=C(CCC)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3259.8	Semi standard non polar	33892256
4,6-Docosanedione,2TBDMS,isomer #3	CCCCCCCCCCCCCCCC=C(C=C(CCC)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	2984.8	Standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 4,6-Docosanedione GC-MS (Non-derivatized) - 70eV, Positive	splash10-03dj-5980000000-faa22feca75da17571c1	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 4,6-Docosanedione 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 - 4,6-Docosanedione 10V, Positive-QTOF	splash10-000i-1029000000-c3513f61d4f8e679f302	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4,6-Docosanedione 20V, Positive-QTOF	splash10-0fk9-9371000000-572385bd185260eb1374	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4,6-Docosanedione 40V, Positive-QTOF	splash10-0096-9370000000-05403d3dc5e235c8716a	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4,6-Docosanedione 10V, Negative-QTOF	splash10-000i-0019000000-52b09b4a84a47bc01a2e	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4,6-Docosanedione 20V, Negative-QTOF	splash10-000i-6269000000-654add99c50ba9b54b0f	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4,6-Docosanedione 40V, Negative-QTOF	splash10-0a4l-9131000000-8e9fb536a75b53c38e22	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4,6-Docosanedione 10V, Positive-QTOF	splash10-0079-2009000000-3df37157a6cd6f0fdb8e	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4,6-Docosanedione 20V, Positive-QTOF	splash10-0fe0-9215000000-99f681405b27e02d873d	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4,6-Docosanedione 40V, Positive-QTOF	splash10-0a4l-9000000000-263ca6a450da1bdfc523	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4,6-Docosanedione 10V, Negative-QTOF	splash10-000i-0009000000-79405c9f142396a61339	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4,6-Docosanedione 20V, Negative-QTOF	splash10-000i-9214000000-71d77e6409b156c74ca5	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4,6-Docosanedione 40V, Negative-QTOF	splash10-0ap3-9010000000-59b78e85bbaa16fb5ba9	2021-09-22	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Membrane

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB014261

KNApSAcK ID

Not Available

Chemspider ID

30777129

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

131751804

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

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

Showing metabocard for 4,6-Docosanedione (HMDB0035569)

MOL for HMDB0035569 (4,6-Docosanedione)

3D MOL for HMDB0035569 (4,6-Docosanedione)

3D SDF for HMDB0035569 (4,6-Docosanedione)

3D-SDF for HMDB0035569 (4,6-Docosanedione)

PDB for HMDB0035569 (4,6-Docosanedione)

3D PDB for HMDB0035569 (4,6-Docosanedione)

SMILES for HMDB0035569 (4,6-Docosanedione)

INCHI for HMDB0035569 (4,6-Docosanedione)

Structure for HMDB0035569 (4,6-Docosanedione)

3D Structure for HMDB0035569 (4,6-Docosanedione)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra