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Identification Taxonomy Ontology Physical properties Spectra Biological properties Concentrations Links References enzymes (1) Show 1 protein XML

enzymes (1) Show 1 protein

Record Information

Version

5.0

Status

Detected and Quantified

Creation Date

2006-08-13 23:38:34 UTC

Update Date

2022-03-07 02:49:21 UTC

HMDB ID

HMDB0004668

Secondary Accession Numbers

HMDB04668

Metabolite Identification

Common Name

13-OxoODE

Description

13-oxoODE is produced from 13-HODE by a NAD+-dependent dehydrogenase present in rat colonic mucosa. 13-OxoODE has been shown to stimulate cell proliferation when instilled intrarectally in rats. 13-OxoODE has also been detected in preparations of rabbit reticulocyte plasma and mitochondrial membranes, mostly esterified to phospholipids. Production of 13-oxoODE is putatively linked to the maturation of reticulocytes to erythrocytes through the activity of 15-LO.

Structure

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

HMDB0004668
     RDKit          3D
13-OxoODE
 51 50  0  0  0  0  0  0  0  0999 V2000
    6.5633    0.0655    0.6878 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7580    0.0183   -0.7805 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5382    0.2225   -1.6059 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8559    1.5188   -1.4920 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2508    1.9318   -0.2178 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1492    1.1337    0.3145 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8316    1.3020    1.5302 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3814    0.1648   -0.4264 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3796   -0.5312    0.1357 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5835   -1.5118   -0.5683 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3737   -2.1396    0.0609 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7474   -1.9599    1.4487 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2132   -1.4887    1.4795 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3734   -0.1910    0.7340 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7955    0.3087    0.7579 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7722   -0.6373    0.1351 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1657   -0.0741    0.2173 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3384    1.2361   -0.4977 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0223    1.0641   -1.9433 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9640    1.4063   -2.4796 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0484    0.4593   -2.6993 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9594    0.9954    1.1642 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5375   -0.1390    1.0074 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2263   -0.7556    1.1412 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3041   -0.9207   -1.1074 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4963    0.8337   -1.0493 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8092   -0.6073   -1.3909 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8116    0.0219   -2.6866 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6223    2.3188   -1.7705 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1193    1.6188   -2.3606 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8391    2.9909   -0.4074 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9950    2.1245    0.5960 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5721   -0.0325   -1.4581 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2071   -0.3033    1.1655 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7924   -1.7305   -1.6446 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9417   -2.8706   -0.5400 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2029   -1.2209    2.0432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7249   -2.9087    2.0466 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8590   -2.2414    0.9859 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5530   -1.3587    2.5313 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7426    0.5929    1.2125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9871   -0.2862   -0.3036 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7891    1.2504    0.1473 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0616    0.5359    1.8113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5646   -0.7735   -0.9597 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7565   -1.6399    0.6336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4956    0.0461    1.2756 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8639   -0.8060   -0.2844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4073    1.5309   -0.3892 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6635    1.9801   -0.0342 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1554   -0.5441   -2.5555 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  2  0
  6  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  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  1  0
 18 19  1  0
 19 20  2  0
 19 21  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  2 25  1  0
  2 26  1  0
  3 27  1  0
  3 28  1  0
  4 29  1  0
  4 30  1  0
  5 31  1  0
  5 32  1  0
  8 33  1  0
  9 34  1  0
 10 35  1  0
 11 36  1  0
 12 37  1  0
 12 38  1  0
 13 39  1  0
 13 40  1  0
 14 41  1  0
 14 42  1  0
 15 43  1  0
 15 44  1  0
 16 45  1  0
 16 46  1  0
 17 47  1  0
 17 48  1  0
 18 49  1  0
 18 50  1  0
 21 51  1  0
M  END


  Mrv0541 02231219582D          

 21 20  0  0  0  0            999 V2000
   24.1800  -19.4576    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   24.8946  -18.2201    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.4642  -14.5075    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   22.7511  -16.1576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.0366  -15.7451    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.7511  -16.9826    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.0366  -14.9200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.4656  -17.3951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.3221  -14.5075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.4656  -18.2201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.0352  -13.6825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.3208  -13.2700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.7497  -13.2700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6062  -13.6825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.3221  -13.6825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.1800  -18.6326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.4642  -13.6825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.8917  -13.2700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.6076  -13.2700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.1787  -13.2700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.8932  -13.6825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1 16  1  0  0  0  0
  2 16  2  0  0  0  0
  3 17  2  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  5  7  1  0  0  0  0
  6  8  1  0  0  0  0
  7  9  1  0  0  0  0
  8 10  1  0  0  0  0
  9 15  1  0  0  0  0
 10 16  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 12 14  1  0  0  0  0
 13 17  1  0  0  0  0
 14 18  1  0  0  0  0
 15 19  2  0  0  0  0
 17 20  1  0  0  0  0
 19 21  1  0  0  0  0
 20 21  2  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0004668

> <DATABASE_NAME>
hmdb

> <SMILES>
CCCCCC(=O)\C=C\C=C/CCCCCCCC(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C18H30O3/c1-2-3-11-14-17(19)15-12-9-7-5-4-6-8-10-13-16-18(20)21/h7,9,12,15H,2-6,8,10-11,13-14,16H2,1H3,(H,20,21)/b9-7-,15-12+

> <INCHI_KEY>
JHXAZBBVQSRKJR-BSZOFBHHSA-N

> <FORMULA>
C18H30O3

> <MOLECULAR_WEIGHT>
294.429

> <EXACT_MASS>
294.219494826

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_AVERAGE_POLARIZABILITY>
36.073522142850926

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(9Z,11E)-13-oxooctadeca-9,11-dienoic acid

> <ALOGPS_LOGP>
5.66

> <JCHEM_LOGP>
5.602404215333333

> <ALOGPS_LOGS>
-5.35

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.988167284021987

> <JCHEM_PKA_STRONGEST_BASIC>
-4.577074788947507

> <JCHEM_POLAR_SURFACE_AREA>
54.37

> <JCHEM_REFRACTIVITY>
89.13689999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
14

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.30e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
13-Oxo-ODE

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0004668
     RDKit          3D
13-OxoODE
 51 50  0  0  0  0  0  0  0  0999 V2000
    6.5633    0.0655    0.6878 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7580    0.0183   -0.7805 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5382    0.2225   -1.6059 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8559    1.5188   -1.4920 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2508    1.9318   -0.2178 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1492    1.1337    0.3145 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8316    1.3020    1.5302 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3814    0.1648   -0.4264 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3796   -0.5312    0.1357 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5835   -1.5118   -0.5683 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3737   -2.1396    0.0609 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7474   -1.9599    1.4487 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2132   -1.4887    1.4795 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3734   -0.1910    0.7340 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7955    0.3087    0.7579 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7722   -0.6373    0.1351 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1657   -0.0741    0.2173 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3384    1.2361   -0.4977 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0223    1.0641   -1.9433 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9640    1.4063   -2.4796 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0484    0.4593   -2.6993 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9594    0.9954    1.1642 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5375   -0.1390    1.0074 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2263   -0.7556    1.1412 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3041   -0.9207   -1.1074 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4963    0.8337   -1.0493 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8092   -0.6073   -1.3909 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8116    0.0219   -2.6866 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6223    2.3188   -1.7705 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1193    1.6188   -2.3606 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8391    2.9909   -0.4074 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9950    2.1245    0.5960 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5721   -0.0325   -1.4581 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2071   -0.3033    1.1655 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7924   -1.7305   -1.6446 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9417   -2.8706   -0.5400 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2029   -1.2209    2.0432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7249   -2.9087    2.0466 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8590   -2.2414    0.9859 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5530   -1.3587    2.5313 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7426    0.5929    1.2125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9871   -0.2862   -0.3036 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7891    1.2504    0.1473 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0616    0.5359    1.8113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5646   -0.7735   -0.9597 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7565   -1.6399    0.6336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4956    0.0461    1.2756 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8639   -0.8060   -0.2844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4073    1.5309   -0.3892 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6635    1.9801   -0.0342 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1554   -0.5441   -2.5555 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  2  0
  6  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  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  1  0
 18 19  1  0
 19 20  2  0
 19 21  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  2 25  1  0
  2 26  1  0
  3 27  1  0
  3 28  1  0
  4 29  1  0
  4 30  1  0
  5 31  1  0
  5 32  1  0
  8 33  1  0
  9 34  1  0
 10 35  1  0
 11 36  1  0
 12 37  1  0
 12 38  1  0
 13 39  1  0
 13 40  1  0
 14 41  1  0
 14 42  1  0
 15 43  1  0
 15 44  1  0
 16 45  1  0
 16 46  1  0
 17 47  1  0
 17 48  1  0
 18 49  1  0
 18 50  1  0
 21 51  1  0
M  END

HEADER    PROTEIN                                 23-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-FEB-12         0                                  
HETATM    1  O   UNK     0      45.136 -36.321   0.000  0.00  0.00           O+0
HETATM    2  O   UNK     0      46.470 -34.011   0.000  0.00  0.00           O+0
HETATM    3  O   UNK     0      34.467 -27.081   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      42.469 -30.161   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      41.135 -29.391   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      42.469 -31.701   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      41.135 -27.851   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      43.802 -32.471   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      39.801 -27.081   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      43.802 -34.011   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      31.799 -25.541   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      30.465 -24.771   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      33.133 -24.771   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      29.132 -25.541   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      39.801 -25.541   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      45.136 -34.781   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      34.467 -25.541   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      27.798 -24.771   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      38.468 -24.771   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      35.800 -24.771   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      37.134 -25.541   0.000  0.00  0.00           C+0
CONECT    1   16                                                            
CONECT    2   16                                                            
CONECT    3   17                                                            
CONECT    4    5    6                                                       
CONECT    5    4    7                                                       
CONECT    6    4    8                                                       
CONECT    7    5    9                                                       
CONECT    8    6   10                                                       
CONECT    9    7   15                                                       
CONECT   10    8   16                                                       
CONECT   11   12   13                                                       
CONECT   12   11   14                                                       
CONECT   13   11   17                                                       
CONECT   14   12   18                                                       
CONECT   15    9   19                                                       
CONECT   16    1    2   10                                                  
CONECT   17    3   13   20                                                  
CONECT   18   14                                                            
CONECT   19   15   21                                                       
CONECT   20   17   21                                                       
CONECT   21   19   20                                                       
MASTER        0    0    0    0    0    0    0    0   21    0   40    0
END

COMPND    HMDB0004668
HETATM    1  C1  UNL     1       6.563   0.066   0.688  1.00  0.00           C  
HETATM    2  C2  UNL     1       6.758   0.018  -0.781  1.00  0.00           C  
HETATM    3  C3  UNL     1       5.538   0.223  -1.606  1.00  0.00           C  
HETATM    4  C4  UNL     1       4.856   1.519  -1.492  1.00  0.00           C  
HETATM    5  C5  UNL     1       4.251   1.932  -0.218  1.00  0.00           C  
HETATM    6  C6  UNL     1       3.149   1.134   0.315  1.00  0.00           C  
HETATM    7  O1  UNL     1       2.832   1.302   1.530  1.00  0.00           O  
HETATM    8  C7  UNL     1       2.381   0.165  -0.426  1.00  0.00           C  
HETATM    9  C8  UNL     1       1.380  -0.531   0.136  1.00  0.00           C  
HETATM   10  C9  UNL     1       0.583  -1.512  -0.568  1.00  0.00           C  
HETATM   11  C10 UNL     1      -0.374  -2.140   0.061  1.00  0.00           C  
HETATM   12  C11 UNL     1      -0.747  -1.960   1.449  1.00  0.00           C  
HETATM   13  C12 UNL     1      -2.213  -1.489   1.479  1.00  0.00           C  
HETATM   14  C13 UNL     1      -2.373  -0.191   0.734  1.00  0.00           C  
HETATM   15  C14 UNL     1      -3.796   0.309   0.758  1.00  0.00           C  
HETATM   16  C15 UNL     1      -4.772  -0.637   0.135  1.00  0.00           C  
HETATM   17  C16 UNL     1      -6.166  -0.074   0.217  1.00  0.00           C  
HETATM   18  C17 UNL     1      -6.338   1.236  -0.498  1.00  0.00           C  
HETATM   19  C18 UNL     1      -6.022   1.064  -1.943  1.00  0.00           C  
HETATM   20  O2  UNL     1      -4.964   1.406  -2.480  1.00  0.00           O  
HETATM   21  O3  UNL     1      -7.048   0.459  -2.699  1.00  0.00           O  
HETATM   22  H1  UNL     1       6.959   0.995   1.164  1.00  0.00           H  
HETATM   23  H2  UNL     1       5.537  -0.139   1.007  1.00  0.00           H  
HETATM   24  H3  UNL     1       7.226  -0.756   1.141  1.00  0.00           H  
HETATM   25  H4  UNL     1       7.304  -0.921  -1.107  1.00  0.00           H  
HETATM   26  H5  UNL     1       7.496   0.834  -1.049  1.00  0.00           H  
HETATM   27  H6  UNL     1       4.809  -0.607  -1.391  1.00  0.00           H  
HETATM   28  H7  UNL     1       5.812   0.022  -2.687  1.00  0.00           H  
HETATM   29  H8  UNL     1       5.622   2.319  -1.771  1.00  0.00           H  
HETATM   30  H9  UNL     1       4.119   1.619  -2.361  1.00  0.00           H  
HETATM   31  H10 UNL     1       3.839   2.991  -0.407  1.00  0.00           H  
HETATM   32  H11 UNL     1       4.995   2.125   0.596  1.00  0.00           H  
HETATM   33  H12 UNL     1       2.572  -0.032  -1.458  1.00  0.00           H  
HETATM   34  H13 UNL     1       1.207  -0.303   1.166  1.00  0.00           H  
HETATM   35  H14 UNL     1       0.792  -1.730  -1.645  1.00  0.00           H  
HETATM   36  H15 UNL     1      -0.942  -2.871  -0.540  1.00  0.00           H  
HETATM   37  H16 UNL     1      -0.203  -1.221   2.043  1.00  0.00           H  
HETATM   38  H17 UNL     1      -0.725  -2.909   2.047  1.00  0.00           H  
HETATM   39  H18 UNL     1      -2.859  -2.241   0.986  1.00  0.00           H  
HETATM   40  H19 UNL     1      -2.553  -1.359   2.531  1.00  0.00           H  
HETATM   41  H20 UNL     1      -1.743   0.593   1.212  1.00  0.00           H  
HETATM   42  H21 UNL     1      -1.987  -0.286  -0.304  1.00  0.00           H  
HETATM   43  H22 UNL     1      -3.789   1.250   0.147  1.00  0.00           H  
HETATM   44  H23 UNL     1      -4.062   0.536   1.811  1.00  0.00           H  
HETATM   45  H24 UNL     1      -4.565  -0.773  -0.960  1.00  0.00           H  
HETATM   46  H25 UNL     1      -4.757  -1.640   0.634  1.00  0.00           H  
HETATM   47  H26 UNL     1      -6.496   0.046   1.276  1.00  0.00           H  
HETATM   48  H27 UNL     1      -6.864  -0.806  -0.284  1.00  0.00           H  
HETATM   49  H28 UNL     1      -7.407   1.531  -0.389  1.00  0.00           H  
HETATM   50  H29 UNL     1      -5.663   1.980  -0.034  1.00  0.00           H  
HETATM   51  H30 UNL     1      -7.155  -0.544  -2.556  1.00  0.00           H  
CONECT    1    2   22   23   24
CONECT    2    3   25   26
CONECT    3    4   27   28
CONECT    4    5   29   30
CONECT    5    6   31   32
CONECT    6    7    7    8
CONECT    8    9    9   33
CONECT    9   10   34
CONECT   10   11   11   35
CONECT   11   12   36
CONECT   12   13   37   38
CONECT   13   14   39   40
CONECT   14   15   41   42
CONECT   15   16   43   44
CONECT   16   17   45   46
CONECT   17   18   47   48
CONECT   18   19   49   50
CONECT   19   20   20   21
CONECT   21   51
END

HMDB0004668
     RDKit          3D
13-OxoODE
 51 50  0  0  0  0  0  0  0  0999 V2000
    6.5633    0.0655    0.6878 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7580    0.0183   -0.7805 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5382    0.2225   -1.6059 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8559    1.5188   -1.4920 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2508    1.9318   -0.2178 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1492    1.1337    0.3145 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8316    1.3020    1.5302 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3814    0.1648   -0.4264 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3796   -0.5312    0.1357 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5835   -1.5118   -0.5683 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3737   -2.1396    0.0609 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7474   -1.9599    1.4487 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2132   -1.4887    1.4795 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3734   -0.1910    0.7340 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7955    0.3087    0.7579 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7722   -0.6373    0.1351 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1657   -0.0741    0.2173 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3384    1.2361   -0.4977 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0223    1.0641   -1.9433 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9640    1.4063   -2.4796 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0484    0.4593   -2.6993 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9594    0.9954    1.1642 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5375   -0.1390    1.0074 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2263   -0.7556    1.1412 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3041   -0.9207   -1.1074 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4963    0.8337   -1.0493 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8092   -0.6073   -1.3909 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8116    0.0219   -2.6866 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6223    2.3188   -1.7705 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1193    1.6188   -2.3606 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8391    2.9909   -0.4074 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9950    2.1245    0.5960 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5721   -0.0325   -1.4581 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2071   -0.3033    1.1655 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7924   -1.7305   -1.6446 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9417   -2.8706   -0.5400 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2029   -1.2209    2.0432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7249   -2.9087    2.0466 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8590   -2.2414    0.9859 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5530   -1.3587    2.5313 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7426    0.5929    1.2125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9871   -0.2862   -0.3036 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7891    1.2504    0.1473 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0616    0.5359    1.8113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5646   -0.7735   -0.9597 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7565   -1.6399    0.6336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4956    0.0461    1.2756 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8639   -0.8060   -0.2844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4073    1.5309   -0.3892 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6635    1.9801   -0.0342 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1554   -0.5441   -2.5555 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  2  0
  6  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  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  1  0
 18 19  1  0
 19 20  2  0
 19 21  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  2 25  1  0
  2 26  1  0
  3 27  1  0
  3 28  1  0
  4 29  1  0
  4 30  1  0
  5 31  1  0
  5 32  1  0
  8 33  1  0
  9 34  1  0
 10 35  1  0
 11 36  1  0
 12 37  1  0
 12 38  1  0
 13 39  1  0
 13 40  1  0
 14 41  1  0
 14 42  1  0
 15 43  1  0
 15 44  1  0
 16 45  1  0
 16 46  1  0
 17 47  1  0
 17 48  1  0
 18 49  1  0
 18 50  1  0
 21 51  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
13-Keto-9Z,11E-octadecadienoic acid	ChEBI
13-KetoODE	ChEBI
13-KODE	ChEBI
13-oxo-ODE	ChEBI
(9Z,11E)-13-Oxooctadeca-9,11-dienoic acid	Kegg
13-Keto-9Z,11E-octadecadienoate	Generator
(9Z,11E)-13-Oxooctadeca-9,11-dienoate	Generator
13-KODDA	HMDB
13-Keto-9,11,-octadecadienoic acid	HMDB
13-oxo-9,11-Octadecadienoic acid	HMDB
13-Oxooctadecadienoic acid	HMDB
13-OxoODE	ChEBI

Chemical Formula

C₁₈H₃₀O₃

Average Molecular Weight

294.429

Monoisotopic Molecular Weight

294.219494826

IUPAC Name

(9Z,11E)-13-oxooctadeca-9,11-dienoic acid

Traditional Name

13-Oxo-ODE

CAS Registry Number

Not Available

SMILES

CCCCCC(=O)\C=C\C=C/CCCCCCCC(O)=O

InChI Identifier

InChI=1S/C18H30O3/c1-2-3-11-14-17(19)15-12-9-7-5-4-6-8-10-13-16-18(20)21/h7,9,12,15H,2-6,8,10-11,13-14,16H2,1H3,(H,20,21)/b9-7-,15-12+

InChI Key

JHXAZBBVQSRKJR-BSZOFBHHSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as lineolic acids and derivatives. These are derivatives of lineolic acid. Lineolic acid is a polyunsaturated omega-6 18 carbon long fatty acid, with two CC double bonds at the 9- and 12-positions.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Lineolic acids and derivatives

Direct Parent

Lineolic acids and derivatives

Alternative Parents

Substituents

Octadecanoid
Long-chain fatty acid
Unsaturated fatty acid
Fatty acid
Acryloyl-group
Enone
Alpha,beta-unsaturated ketone
Ketone
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic oxide
Organic oxygen compound
Organooxygen compound
Hydrocarbon derivative
Carbonyl group
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

enone (CHEBI:68947 )
OxoODE (CHEBI:68947 )
Other Octadecanoids (C14765 )
Other Octadecanoids (LMFA02000016 )

Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 18953024)

Cellular substructure

Extracellular (HMDB: HMDB0004668)
Membrane (HMDB: HMDB0004668)

Greylag goose (FooDB: FOOD00368)
Guinea hen (FooDB: FOOD00373)
Ostrich (FooDB: FOOD00422)
Velvet duck (FooDB: FOOD00427)
Pheasant (FooDB: FOOD00430)
Squab (FooDB: FOOD00481)
Turkey (FooDB: FOOD00494)
Quail (FooDB: FOOD00541)
Anatidae (FooDB: FOOD00576)
Rock ptarmigan (FooDB: FOOD00597)
Columbidae (Dove, Pigeon) (FooDB: FOOD00610)
Chicken (FooDB: FOOD00329)
Mallard duck (FooDB: FOOD00353)
Emu (FooDB: FOOD00360)

Equine

Horse (FooDB: FOOD00378)

Lagomorph

Ovis

Sheep (Mutton, Lamb) (FooDB: FOOD00473)

Bovine

Venison

Deer (FooDB: FOOD00524)
Mule deer (FooDB: FOOD00348)
Elk (FooDB: FOOD00359)

Caprae

Domestic goat (FooDB: FOOD00529)

Swine

Domestic pig (FooDB: FOOD00536)
Wild boar (FooDB: FOOD00307)

Process

Not Available

Role

Not Available

Physical Properties

State

Solid

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

Experimental Collision Cross Sections

Adduct Type	Data Source	CCS Value (Å²)	Reference
[M-H]-	Not Available	180.433	http://allccs.zhulab.cn/database/detail?ID=AllCCS00001899
[M+H]+	Not Available	179.4	http://allccs.zhulab.cn/database/detail?ID=AllCCS00001899

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.0013 g/L	ALOGPS
logP	5.66	ALOGPS
logP	5.6	ChemAxon
logS	-5.4	ALOGPS
pKa (Strongest Acidic)	4.99	ChemAxon
pKa (Strongest Basic)	-4.6	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	54.37 Å²	ChemAxon
Rotatable Bond Count	14	ChemAxon
Refractivity	89.14 m³·mol⁻¹	ChemAxon
Polarizability	36.07 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]+	181.843	30932474
DeepCCS	[M-H]-	179.485	30932474
DeepCCS	[M-2H]-	212.371	30932474
DeepCCS	[M+Na]+	187.936	30932474
AllCCS	[M+H]+	179.1	32859911
AllCCS	[M+H-H2O]+	176.1	32859911
AllCCS	[M+NH4]+	181.9	32859911
AllCCS	[M+Na]+	182.7	32859911
AllCCS	[M-H]-	179.5	32859911
AllCCS	[M+Na-2H]-	181.0	32859911
AllCCS	[M+HCOO]-	182.7	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
13-OxoODE	CCCCCC(=O)\C=C\C=C/CCCCCCCC(O)=O	3778.8	Standard polar	33892256
13-OxoODE	CCCCCC(=O)\C=C\C=C/CCCCCCCC(O)=O	2279.9	Standard non polar	33892256
13-OxoODE	CCCCCC(=O)\C=C\C=C/CCCCCCCC(O)=O	2464.7	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
13-OxoODE,1TMS,isomer #1	CCCCCC(=O)/C=C/C=C\CCCCCCCC(=O)O[Si](C)(C)C	2506.4	Semi standard non polar	33892256
13-OxoODE,1TMS,isomer #2	CCCCC=C(/C=C/C=C\CCCCCCCC(=O)O)O[Si](C)(C)C	2659.4	Semi standard non polar	33892256
13-OxoODE,2TMS,isomer #1	CCCCC=C(/C=C/C=C\CCCCCCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C	2643.6	Semi standard non polar	33892256
13-OxoODE,2TMS,isomer #1	CCCCC=C(/C=C/C=C\CCCCCCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C	2546.5	Standard non polar	33892256
13-OxoODE,2TMS,isomer #1	CCCCC=C(/C=C/C=C\CCCCCCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C	2652.6	Standard polar	33892256
13-OxoODE,1TBDMS,isomer #1	CCCCCC(=O)/C=C/C=C\CCCCCCCC(=O)O[Si](C)(C)C(C)(C)C	2756.7	Semi standard non polar	33892256
13-OxoODE,1TBDMS,isomer #2	CCCCC=C(/C=C/C=C\CCCCCCCC(=O)O)O[Si](C)(C)C(C)(C)C	2906.7	Semi standard non polar	33892256
13-OxoODE,2TBDMS,isomer #1	CCCCC=C(/C=C/C=C\CCCCCCCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3135.4	Semi standard non polar	33892256
13-OxoODE,2TBDMS,isomer #1	CCCCC=C(/C=C/C=C\CCCCCCCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	2933.4	Standard non polar	33892256
13-OxoODE,2TBDMS,isomer #1	CCCCC=C(/C=C/C=C\CCCCCCCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	2806.0	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 13-OxoODE GC-MS (Non-derivatized) - 70eV, Positive	splash10-004j-6930000000-d10bec81e9ec9e716fa2	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 13-OxoODE GC-MS (1 TMS) - 70eV, Positive	splash10-0g2i-9750000000-bfda7e2eea95619a49f0	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 13-OxoODE 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 - 13-OxoODE 10V, Positive-QTOF	splash10-004j-0190000000-a96e4ea1acf25f5bb5a3	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 13-OxoODE 20V, Positive-QTOF	splash10-056s-5790000000-14707a3a66247416895c	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 13-OxoODE 40V, Positive-QTOF	splash10-05g3-9720000000-cdeb3fe3585fb2aabaf6	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 13-OxoODE 10V, Negative-QTOF	splash10-0006-0090000000-09978321bcbe7824cadf	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 13-OxoODE 20V, Negative-QTOF	splash10-002e-2290000000-e322d98207fbdbed5fce	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 13-OxoODE 40V, Negative-QTOF	splash10-052f-9430000000-6bf81e4857713e8781c5	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 13-OxoODE 10V, Negative-QTOF	splash10-0006-0090000000-70cae714b15b662c6aa1	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 13-OxoODE 20V, Negative-QTOF	splash10-002f-2590000000-dba8b2a106352cfef082	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 13-OxoODE 40V, Negative-QTOF	splash10-052f-9530000000-71771e55577a451c8cb4	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 13-OxoODE 10V, Positive-QTOF	splash10-004j-1490000000-80caae23bc80ab7cea2c	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 13-OxoODE 20V, Positive-QTOF	splash10-0aba-8940000000-d8f1355540068e477746	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 13-OxoODE 40V, Positive-QTOF	splash10-0apm-9200000000-cad11773185d75e4951e	2021-09-25	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Extracellular
Membrane

Biospecimen Locations

Blood

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Detected and Quantified	0.00049 +/- 0.00004 uM	Adult (>18 years old)	Both	Normal	20671299	details
Blood	Detected and Quantified	0.00482 (0.00414-0.00550) uM	Adult (>18 years old)	Both	Normal	18953024 21359215	details
Blood	Detected and Quantified	0.00482 +/- 0.00068 uM	Adult (>18 years old)	Both	Normal	21359215	details
Blood	Detected and Quantified	0.0017 +/- 0.0012 uM	Adult (>18 years old)	Both	Normal	21359215	details

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

FDB023396

KNApSAcK ID

Not Available

Chemspider ID

4949634

KEGG Compound ID

C14765

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

6446027

PDB ID

Not Available

ChEBI ID

68947

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

Not Available

Enzymes

Enzyme Details

1. Retinol dehydrogenase 13

General function:: Involved in oxidoreductase activity
Specific function:: Does not exhibit retinol dehydrogenase (RDH) activity in vitro
Gene Name:: RDH13
Uniprot ID:: Q8NBN7
Molecular weight:: 35931.8

Showing metabocard for 13-OxoODE (HMDB0004668)

MOL for HMDB0004668 (13-OxoODE)

3D MOL for HMDB0004668 (13-OxoODE)

3D SDF for HMDB0004668 (13-OxoODE)

3D-SDF for HMDB0004668 (13-OxoODE)

PDB for HMDB0004668 (13-OxoODE)

3D PDB for HMDB0004668 (13-OxoODE)

SMILES for HMDB0004668 (13-OxoODE)

INCHI for HMDB0004668 (13-OxoODE)

Structure for HMDB0004668 (13-OxoODE)

3D Structure for HMDB0004668 (13-OxoODE)

Experimental Collision Cross Sections

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

Enzymes