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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 17:40:11 UTC

Update Date

2022-03-07 02:52:46 UTC

HMDB ID

HMDB0030981

Secondary Accession Numbers

HMDB30981

Metabolite Identification

Common Name

11-Oxooctadecanoic acid

Description

11-Oxooctadecanoic acid belongs to the class of organic compounds known as long-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 13 and 21 carbon atoms. Based on a literature review a small amount of articles have been published on 11-Oxooctadecanoic acid.

Structure

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

HMDB0030981
     RDKit          3D
11-Oxooctadecanoic acid
 55 54  0  0  0  0  0  0  0  0999 V2000
   -4.2892    2.8630    0.9528 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9813    1.8594    0.0500 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7889    0.4911    0.6878 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2947    0.2647    0.7581 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9743   -1.0972    1.3899 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5772   -2.2004    0.5865 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1155   -2.2868   -0.8360 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6608   -2.5469   -0.8903 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0525   -2.7280    0.1406 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9194   -2.5924   -2.1860 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5514   -2.8090   -2.0051 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2048   -1.6940   -1.2130 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0387   -0.3700   -1.8743 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6789    0.7159   -1.0589 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1379    0.4509   -0.9036 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8356    1.5373   -0.0974 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2889    1.1325   -0.0278 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1558    2.0816    0.7312 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7583    2.2414    2.1372 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4108    3.0679    2.8349 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7298    1.5552    2.7426 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2470    3.0757    0.6249 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8942    3.7952    0.9144 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2044    2.4890    2.0015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4233    1.8969   -0.9256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0253    2.0985   -0.1516 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1534    0.5264    1.7322 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3194   -0.2984    0.1622 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7836    1.0256    1.3630 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8009    0.2650   -0.2336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8812   -1.1227    1.4768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3541   -1.1161    2.4420 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2995   -3.1649    1.1126 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6874   -2.1681    0.6707 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3355   -1.3326   -1.3678 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6958   -3.0600   -1.4049 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3180   -3.5045   -2.7160 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1405   -1.6955   -2.8020 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6566   -3.7821   -1.4420 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0346   -2.9220   -2.9759 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3040   -1.9314   -1.2320 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9259   -1.6507   -0.1690 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0232   -0.1358   -2.1117 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5291   -0.4426   -2.8882 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1440    0.8072   -0.0903 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4841    1.6862   -1.5968 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3193   -0.4860   -0.3333 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6315    0.3670   -1.8686 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7746    2.5251   -0.6322 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3673    1.6664    0.8801 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3639    0.0905    0.3724 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6999    1.0606   -1.0665 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2029    1.7072    0.7211 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1014    3.0660    0.2181 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9107    0.7291    3.3187 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  2  0
  8 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  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
  6 33  1  0
  6 34  1  0
  7 35  1  0
  7 36  1  0
 10 37  1  0
 10 38  1  0
 11 39  1  0
 11 40  1  0
 12 41  1  0
 12 42  1  0
 13 43  1  0
 13 44  1  0
 14 45  1  0
 14 46  1  0
 15 47  1  0
 15 48  1  0
 16 49  1  0
 16 50  1  0
 17 51  1  0
 17 52  1  0
 18 53  1  0
 18 54  1  0
 21 55  1  0
M  END


  Mrv0541 05061305382D          

 21 20  0  0  0  0            999 V2000
    9.1855    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9000    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6145    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3289    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.7592    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.0447    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.4737    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0434    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.3302    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.1881    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.7579    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6158    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.9026    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4724    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.9013    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.6171    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.1868    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.3315    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.1868    4.8908    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   22.0460    6.1283    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   21.3315    4.8908    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0  0  0  0
  3  2  1  0  0  0  0
  4  3  1  0  0  0  0
  6  5  1  0  0  0  0
  7  5  1  0  0  0  0
  8  4  1  0  0  0  0
  9  6  1  0  0  0  0
 10  7  1  0  0  0  0
 11  8  1  0  0  0  0
 12  9  1  0  0  0  0
 13 10  1  0  0  0  0
 14 11  1  0  0  0  0
 15 12  1  0  0  0  0
 16 13  1  0  0  0  0
 17 14  1  0  0  0  0
 17 15  1  0  0  0  0
 18 16  1  0  0  0  0
 19 17  2  0  0  0  0
 20 18  2  0  0  0  0
 21 18  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0030981

> <DATABASE_NAME>
hmdb

> <SMILES>
CCCCCCCC(=O)CCCCCCCCCC(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C18H34O3/c1-2-3-4-8-11-14-17(19)15-12-9-6-5-7-10-13-16-18(20)21/h2-16H2,1H3,(H,20,21)

> <INCHI_KEY>
ZWXGGJPQIPPKPP-UHFFFAOYSA-N

> <FORMULA>
C18H34O3

> <MOLECULAR_WEIGHT>
298.4608

> <EXACT_MASS>
298.250794954

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_AVERAGE_POLARIZABILITY>
38.25896190340737

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
11-oxooctadecanoic acid

> <ALOGPS_LOGP>
5.87

> <JCHEM_LOGP>
5.966502382333333

> <ALOGPS_LOGS>
-5.37

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.9520196552287805

> <JCHEM_PKA_STRONGEST_BASIC>
-7.346983285909792

> <JCHEM_POLAR_SURFACE_AREA>
54.370000000000005

> <JCHEM_REFRACTIVITY>
86.92699999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
16

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.27e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
11-oxooctadecanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0030981
     RDKit          3D
11-Oxooctadecanoic acid
 55 54  0  0  0  0  0  0  0  0999 V2000
   -4.2892    2.8630    0.9528 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9813    1.8594    0.0500 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7889    0.4911    0.6878 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2947    0.2647    0.7581 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9743   -1.0972    1.3899 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5772   -2.2004    0.5865 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1155   -2.2868   -0.8360 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6608   -2.5469   -0.8903 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0525   -2.7280    0.1406 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9194   -2.5924   -2.1860 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5514   -2.8090   -2.0051 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2048   -1.6940   -1.2130 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0387   -0.3700   -1.8743 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6789    0.7159   -1.0589 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1379    0.4509   -0.9036 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8356    1.5373   -0.0974 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2889    1.1325   -0.0278 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1558    2.0816    0.7312 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7583    2.2414    2.1372 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4108    3.0679    2.8349 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7298    1.5552    2.7426 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2470    3.0757    0.6249 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8942    3.7952    0.9144 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2044    2.4890    2.0015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4233    1.8969   -0.9256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0253    2.0985   -0.1516 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1534    0.5264    1.7322 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3194   -0.2984    0.1622 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7836    1.0256    1.3630 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8009    0.2650   -0.2336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8812   -1.1227    1.4768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3541   -1.1161    2.4420 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2995   -3.1649    1.1126 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6874   -2.1681    0.6707 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3355   -1.3326   -1.3678 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6958   -3.0600   -1.4049 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3180   -3.5045   -2.7160 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1405   -1.6955   -2.8020 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6566   -3.7821   -1.4420 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0346   -2.9220   -2.9759 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3040   -1.9314   -1.2320 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9259   -1.6507   -0.1690 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0232   -0.1358   -2.1117 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5291   -0.4426   -2.8882 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1440    0.8072   -0.0903 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4841    1.6862   -1.5968 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3193   -0.4860   -0.3333 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6315    0.3670   -1.8686 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7746    2.5251   -0.6322 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3673    1.6664    0.8801 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3639    0.0905    0.3724 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6999    1.0606   -1.0665 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2029    1.7072    0.7211 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1014    3.0660    0.2181 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9107    0.7291    3.3187 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  2  0
  8 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  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
  6 33  1  0
  6 34  1  0
  7 35  1  0
  7 36  1  0
 10 37  1  0
 10 38  1  0
 11 39  1  0
 11 40  1  0
 12 41  1  0
 12 42  1  0
 13 43  1  0
 13 44  1  0
 14 45  1  0
 14 46  1  0
 15 47  1  0
 15 48  1  0
 16 49  1  0
 16 50  1  0
 17 51  1  0
 17 52  1  0
 18 53  1  0
 18 54  1  0
 21 55  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      17.146  11.439   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      18.480  10.669   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      19.814  11.439   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      21.147  10.669   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      33.151  11.439   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      31.817  10.669   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      34.484  10.669   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      22.481  11.439   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      30.483  11.439   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      35.818  11.439   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      23.815  10.669   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      29.149  10.669   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      37.152  10.669   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      25.148  11.439   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      27.816  11.439   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      38.485  11.439   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      26.482  10.669   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      39.819  10.669   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      26.482   9.129   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      41.153  11.439   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      39.819   9.129   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    8                                                       
CONECT    5    6    7                                                       
CONECT    6    5    9                                                       
CONECT    7    5   10                                                       
CONECT    8    4   11                                                       
CONECT    9    6   12                                                       
CONECT   10    7   13                                                       
CONECT   11    8   14                                                       
CONECT   12    9   15                                                       
CONECT   13   10   16                                                       
CONECT   14   11   17                                                       
CONECT   15   12   17                                                       
CONECT   16   13   18                                                       
CONECT   17   14   15   19                                                  
CONECT   18   16   20   21                                                  
CONECT   19   17                                                            
CONECT   20   18                                                            
CONECT   21   18                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   40    0
END

COMPND    HMDB0030981
HETATM    1  C1  UNL     1      -4.289   2.863   0.953  1.00  0.00           C  
HETATM    2  C2  UNL     1      -4.981   1.859   0.050  1.00  0.00           C  
HETATM    3  C3  UNL     1      -4.789   0.491   0.688  1.00  0.00           C  
HETATM    4  C4  UNL     1      -3.295   0.265   0.758  1.00  0.00           C  
HETATM    5  C5  UNL     1      -2.974  -1.097   1.390  1.00  0.00           C  
HETATM    6  C6  UNL     1      -3.577  -2.200   0.587  1.00  0.00           C  
HETATM    7  C7  UNL     1      -3.115  -2.287  -0.836  1.00  0.00           C  
HETATM    8  C8  UNL     1      -1.661  -2.547  -0.890  1.00  0.00           C  
HETATM    9  O1  UNL     1      -1.053  -2.728   0.141  1.00  0.00           O  
HETATM   10  C9  UNL     1      -0.919  -2.592  -2.186  1.00  0.00           C  
HETATM   11  C10 UNL     1       0.551  -2.809  -2.005  1.00  0.00           C  
HETATM   12  C11 UNL     1       1.205  -1.694  -1.213  1.00  0.00           C  
HETATM   13  C12 UNL     1       1.039  -0.370  -1.874  1.00  0.00           C  
HETATM   14  C13 UNL     1       1.679   0.716  -1.059  1.00  0.00           C  
HETATM   15  C14 UNL     1       3.138   0.451  -0.904  1.00  0.00           C  
HETATM   16  C15 UNL     1       3.836   1.537  -0.097  1.00  0.00           C  
HETATM   17  C16 UNL     1       5.289   1.133  -0.028  1.00  0.00           C  
HETATM   18  C17 UNL     1       6.156   2.082   0.731  1.00  0.00           C  
HETATM   19  C18 UNL     1       5.758   2.241   2.137  1.00  0.00           C  
HETATM   20  O2  UNL     1       6.411   3.068   2.835  1.00  0.00           O  
HETATM   21  O3  UNL     1       4.730   1.555   2.743  1.00  0.00           O  
HETATM   22  H1  UNL     1      -3.247   3.076   0.625  1.00  0.00           H  
HETATM   23  H2  UNL     1      -4.894   3.795   0.914  1.00  0.00           H  
HETATM   24  H3  UNL     1      -4.204   2.489   2.001  1.00  0.00           H  
HETATM   25  H4  UNL     1      -4.423   1.897  -0.926  1.00  0.00           H  
HETATM   26  H5  UNL     1      -6.025   2.099  -0.152  1.00  0.00           H  
HETATM   27  H6  UNL     1      -5.153   0.526   1.732  1.00  0.00           H  
HETATM   28  H7  UNL     1      -5.319  -0.298   0.162  1.00  0.00           H  
HETATM   29  H8  UNL     1      -2.784   1.026   1.363  1.00  0.00           H  
HETATM   30  H9  UNL     1      -2.801   0.265  -0.234  1.00  0.00           H  
HETATM   31  H10 UNL     1      -1.881  -1.123   1.477  1.00  0.00           H  
HETATM   32  H11 UNL     1      -3.354  -1.116   2.442  1.00  0.00           H  
HETATM   33  H12 UNL     1      -3.300  -3.165   1.113  1.00  0.00           H  
HETATM   34  H13 UNL     1      -4.687  -2.168   0.671  1.00  0.00           H  
HETATM   35  H14 UNL     1      -3.336  -1.333  -1.368  1.00  0.00           H  
HETATM   36  H15 UNL     1      -3.696  -3.060  -1.405  1.00  0.00           H  
HETATM   37  H16 UNL     1      -1.318  -3.504  -2.716  1.00  0.00           H  
HETATM   38  H17 UNL     1      -1.140  -1.696  -2.802  1.00  0.00           H  
HETATM   39  H18 UNL     1       0.657  -3.782  -1.442  1.00  0.00           H  
HETATM   40  H19 UNL     1       1.035  -2.922  -2.976  1.00  0.00           H  
HETATM   41  H20 UNL     1       2.304  -1.931  -1.232  1.00  0.00           H  
HETATM   42  H21 UNL     1       0.926  -1.651  -0.169  1.00  0.00           H  
HETATM   43  H22 UNL     1      -0.023  -0.136  -2.112  1.00  0.00           H  
HETATM   44  H23 UNL     1       1.529  -0.443  -2.888  1.00  0.00           H  
HETATM   45  H24 UNL     1       1.144   0.807  -0.090  1.00  0.00           H  
HETATM   46  H25 UNL     1       1.484   1.686  -1.597  1.00  0.00           H  
HETATM   47  H26 UNL     1       3.319  -0.486  -0.333  1.00  0.00           H  
HETATM   48  H27 UNL     1       3.632   0.367  -1.869  1.00  0.00           H  
HETATM   49  H28 UNL     1       3.775   2.525  -0.632  1.00  0.00           H  
HETATM   50  H29 UNL     1       3.367   1.666   0.880  1.00  0.00           H  
HETATM   51  H30 UNL     1       5.364   0.091   0.372  1.00  0.00           H  
HETATM   52  H31 UNL     1       5.700   1.061  -1.066  1.00  0.00           H  
HETATM   53  H32 UNL     1       7.203   1.707   0.721  1.00  0.00           H  
HETATM   54  H33 UNL     1       6.101   3.066   0.218  1.00  0.00           H  
HETATM   55  H34 UNL     1       4.911   0.729   3.319  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   33   34
CONECT    7    8   35   36
CONECT    8    9    9   10
CONECT   10   11   37   38
CONECT   11   12   39   40
CONECT   12   13   41   42
CONECT   13   14   43   44
CONECT   14   15   45   46
CONECT   15   16   47   48
CONECT   16   17   49   50
CONECT   17   18   51   52
CONECT   18   19   53   54
CONECT   19   20   20   21
CONECT   21   55
END

HMDB0030981
     RDKit          3D
11-Oxooctadecanoic acid
 55 54  0  0  0  0  0  0  0  0999 V2000
   -4.2892    2.8630    0.9528 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9813    1.8594    0.0500 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7889    0.4911    0.6878 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2947    0.2647    0.7581 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9743   -1.0972    1.3899 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5772   -2.2004    0.5865 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1155   -2.2868   -0.8360 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6608   -2.5469   -0.8903 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0525   -2.7280    0.1406 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9194   -2.5924   -2.1860 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5514   -2.8090   -2.0051 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2048   -1.6940   -1.2130 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0387   -0.3700   -1.8743 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6789    0.7159   -1.0589 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1379    0.4509   -0.9036 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8356    1.5373   -0.0974 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2889    1.1325   -0.0278 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1558    2.0816    0.7312 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7583    2.2414    2.1372 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4108    3.0679    2.8349 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7298    1.5552    2.7426 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2470    3.0757    0.6249 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8942    3.7952    0.9144 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2044    2.4890    2.0015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4233    1.8969   -0.9256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0253    2.0985   -0.1516 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1534    0.5264    1.7322 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3194   -0.2984    0.1622 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7836    1.0256    1.3630 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8009    0.2650   -0.2336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8812   -1.1227    1.4768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3541   -1.1161    2.4420 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2995   -3.1649    1.1126 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6874   -2.1681    0.6707 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3355   -1.3326   -1.3678 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6958   -3.0600   -1.4049 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3180   -3.5045   -2.7160 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1405   -1.6955   -2.8020 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6566   -3.7821   -1.4420 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0346   -2.9220   -2.9759 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3040   -1.9314   -1.2320 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9259   -1.6507   -0.1690 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0232   -0.1358   -2.1117 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5291   -0.4426   -2.8882 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1440    0.8072   -0.0903 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4841    1.6862   -1.5968 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3193   -0.4860   -0.3333 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6315    0.3670   -1.8686 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7746    2.5251   -0.6322 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3673    1.6664    0.8801 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3639    0.0905    0.3724 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6999    1.0606   -1.0665 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2029    1.7072    0.7211 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1014    3.0660    0.2181 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9107    0.7291    3.3187 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  2  0
  8 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  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
  6 33  1  0
  6 34  1  0
  7 35  1  0
  7 36  1  0
 10 37  1  0
 10 38  1  0
 11 39  1  0
 11 40  1  0
 12 41  1  0
 12 42  1  0
 13 43  1  0
 13 44  1  0
 14 45  1  0
 14 46  1  0
 15 47  1  0
 15 48  1  0
 16 49  1  0
 16 50  1  0
 17 51  1  0
 17 52  1  0
 18 53  1  0
 18 54  1  0
 21 55  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
11-Oxooctadecanoate	Generator
11-Ketostearic acid	HMDB
11-Oxostearic acid	HMDB
11-oxo-Octadecanoate	Generator

Chemical Formula

C₁₈H₃₄O₃

Average Molecular Weight

298.4608

Monoisotopic Molecular Weight

298.250794954

IUPAC Name

11-oxooctadecanoic acid

Traditional Name

11-oxooctadecanoic acid

CAS Registry Number

2388-83-2

SMILES

CCCCCCCC(=O)CCCCCCCCCC(O)=O

InChI Identifier

InChI=1S/C18H34O3/c1-2-3-4-8-11-14-17(19)15-12-9-6-5-7-10-13-16-18(20)21/h2-16H2,1H3,(H,20,21)

InChI Key

ZWXGGJPQIPPKPP-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as long-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 13 and 21 carbon atoms.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acids and conjugates

Direct Parent

Long-chain fatty acids

Alternative Parents

Substituents

Long-chain fatty acid
Ketone
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Other Octadecanoids (LMFA02000255 )

Ontology

Not Available

Urine (HMDB: HMDB0030981)

Cellular substructure

Extracellular (HMDB: HMDB0030981)
Membrane (HMDB: HMDB0030981)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0030981)

Source

Endogenous

Endogenous (HMDB: HMDB0030981)

Animal

Animal (HMDB: HMDB0030981)

Exogenous

Food

Food (HMDB: HMDB0030981)

Milk and milk product

Milk and milk products (FooDB: FOOD00863)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid peroxidation (HMDB: HMDB0030981)

Biochemical process

Fatty acid metabolism (HMDB: HMDB0030981)

Cellular process

Cell signaling (HMDB: HMDB0030981)

Biochemical pathway

Lipid metabolism pathway (HMDB: HMDB0030981)

Role

Biological role

Membrane stabilizer (HMDB: HMDB0030981)

Nutrient

Nutrient (HMDB: HMDB0030981)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0030981)

Emulsifier (HMDB: HMDB0030981)

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	65 °C	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.0013 g/L	ALOGPS
logP	5.87	ALOGPS
logP	5.97	ChemAxon
logS	-5.4	ALOGPS
pKa (Strongest Acidic)	4.95	ChemAxon
pKa (Strongest Basic)	-7.3	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	16	ChemAxon
Refractivity	86.93 m³·mol⁻¹	ChemAxon
Polarizability	38.26 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
DarkChem	[M+H]+	178.289	31661259
DarkChem	[M-H]-	176.955	31661259
DeepCCS	[M+H]+	182.483	30932474
DeepCCS	[M-H]-	178.463	30932474
DeepCCS	[M-2H]-	215.206	30932474
DeepCCS	[M+Na]+	191.298	30932474
AllCCS	[M+H]+	183.6	32859911
AllCCS	[M+H-H2O]+	180.7	32859911
AllCCS	[M+NH4]+	186.2	32859911
AllCCS	[M+Na]+	187.0	32859911
AllCCS	[M-H]-	180.9	32859911
AllCCS	[M+Na-2H]-	182.3	32859911
AllCCS	[M+HCOO]-	183.9	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
11-Oxooctadecanoic acid	CCCCCCCC(=O)CCCCCCCCCC(O)=O	3569.6	Standard polar	33892256
11-Oxooctadecanoic acid	CCCCCCCC(=O)CCCCCCCCCC(O)=O	2239.1	Standard non polar	33892256
11-Oxooctadecanoic acid	CCCCCCCC(=O)CCCCCCCCCC(O)=O	2309.5	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
11-Oxooctadecanoic acid,1TMS,isomer #1	CCCCCCCC(=O)CCCCCCCCCC(=O)O[Si](C)(C)C	2408.1	Semi standard non polar	33892256
11-Oxooctadecanoic acid,1TMS,isomer #2	CCCCCCCC(=CCCCCCCCCC(=O)O)O[Si](C)(C)C	2496.4	Semi standard non polar	33892256
11-Oxooctadecanoic acid,1TMS,isomer #3	CCCCCCC=C(CCCCCCCCCC(=O)O)O[Si](C)(C)C	2495.1	Semi standard non polar	33892256
11-Oxooctadecanoic acid,2TMS,isomer #1	CCCCCCCC(=CCCCCCCCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C	2530.8	Semi standard non polar	33892256
11-Oxooctadecanoic acid,2TMS,isomer #1	CCCCCCCC(=CCCCCCCCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C	2499.8	Standard non polar	33892256
11-Oxooctadecanoic acid,2TMS,isomer #2	CCCCCCC=C(CCCCCCCCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C	2534.4	Semi standard non polar	33892256
11-Oxooctadecanoic acid,2TMS,isomer #2	CCCCCCC=C(CCCCCCCCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C	2501.9	Standard non polar	33892256
11-Oxooctadecanoic acid,1TBDMS,isomer #1	CCCCCCCC(=O)CCCCCCCCCC(=O)O[Si](C)(C)C(C)(C)C	2663.5	Semi standard non polar	33892256
11-Oxooctadecanoic acid,1TBDMS,isomer #2	CCCCCCCC(=CCCCCCCCCC(=O)O)O[Si](C)(C)C(C)(C)C	2743.2	Semi standard non polar	33892256
11-Oxooctadecanoic acid,1TBDMS,isomer #3	CCCCCCC=C(CCCCCCCCCC(=O)O)O[Si](C)(C)C(C)(C)C	2744.2	Semi standard non polar	33892256
11-Oxooctadecanoic acid,2TBDMS,isomer #1	CCCCCCCC(=CCCCCCCCCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3038.8	Semi standard non polar	33892256
11-Oxooctadecanoic acid,2TBDMS,isomer #1	CCCCCCCC(=CCCCCCCCCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	2821.5	Standard non polar	33892256
11-Oxooctadecanoic acid,2TBDMS,isomer #2	CCCCCCC=C(CCCCCCCCCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3041.7	Semi standard non polar	33892256
11-Oxooctadecanoic acid,2TBDMS,isomer #2	CCCCCCC=C(CCCCCCCCCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	2822.7	Standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 11-Oxooctadecanoic acid GC-MS (Non-derivatized) - 70eV, Positive	splash10-004i-5910000000-0f65a5abfc4b37fa9c94	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 11-Oxooctadecanoic acid GC-MS (1 TMS) - 70eV, Positive	splash10-00b9-9640000000-2fef956b6e6446511c42	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 11-Oxooctadecanoic acid 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 - 11-Oxooctadecanoic acid 10V, Positive-QTOF	splash10-000t-0190000000-42a9208fadb47105dec8	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 11-Oxooctadecanoic acid 20V, Positive-QTOF	splash10-0f7t-8970000000-6118d494ad7d14a053a2	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 11-Oxooctadecanoic acid 40V, Positive-QTOF	splash10-052g-9410000000-bd46cfc3c4da545d438c	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 11-Oxooctadecanoic acid 10V, Negative-QTOF	splash10-0002-0090000000-df22dbcc7235ae9f7af2	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 11-Oxooctadecanoic acid 20V, Negative-QTOF	splash10-0002-2490000000-9b1f76e77cc7b42ff64c	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 11-Oxooctadecanoic acid 40V, Negative-QTOF	splash10-0a4l-9510000000-d4442abe9a7d80bc6543	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 11-Oxooctadecanoic acid 10V, Negative-QTOF	splash10-0002-0090000000-74e94d5c81ec537c8afe	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 11-Oxooctadecanoic acid 20V, Negative-QTOF	splash10-002b-0190000000-61cac96e6229ba5c9de4	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 11-Oxooctadecanoic acid 40V, Negative-QTOF	splash10-002f-7950000000-42d97df5a9bf9e6a2ff0	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 11-Oxooctadecanoic acid 10V, Positive-QTOF	splash10-01qa-1190000000-afffaf571c3dc7f091b8	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 11-Oxooctadecanoic acid 20V, Positive-QTOF	splash10-03ea-9680000000-df5c029c2e41f046f16b	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 11-Oxooctadecanoic acid 40V, Positive-QTOF	splash10-0a59-9100000000-3927c77612f147a64295	2021-09-22	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Extracellular
Membrane

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB002969

KNApSAcK ID

Not Available

Chemspider ID

4472330

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5312905

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. [PubMed:11413487 ]
Watson AD: Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Lipidomics: a global approach to lipid analysis in biological systems. J Lipid Res. 2006 Oct;47(10):2101-11. Epub 2006 Aug 10. [PubMed:16902246 ]
Sethi JK, Vidal-Puig AJ: Thematic review series: adipocyte biology. Adipose tissue function and plasticity orchestrate nutritional adaptation. J Lipid Res. 2007 Jun;48(6):1253-62. Epub 2007 Mar 20. [PubMed:17374880 ]
Lingwood D, Simons K: Lipid rafts as a membrane-organizing principle. Science. 2010 Jan 1;327(5961):46-50. doi: 10.1126/science.1174621. [PubMed:20044567 ]
(). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .
Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.

Showing metabocard for 11-Oxooctadecanoic acid (HMDB0030981)

MOL for HMDB0030981 (11-Oxooctadecanoic acid)

3D MOL for HMDB0030981 (11-Oxooctadecanoic acid)

3D SDF for HMDB0030981 (11-Oxooctadecanoic acid)

3D-SDF for HMDB0030981 (11-Oxooctadecanoic acid)

PDB for HMDB0030981 (11-Oxooctadecanoic acid)

3D PDB for HMDB0030981 (11-Oxooctadecanoic acid)

SMILES for HMDB0030981 (11-Oxooctadecanoic acid)

INCHI for HMDB0030981 (11-Oxooctadecanoic acid)

Structure for HMDB0030981 (11-Oxooctadecanoic acid)

3D Structure for HMDB0030981 (11-Oxooctadecanoic acid)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra