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Record Information

Version

5.0

Status

Detected and Quantified

Creation Date

2008-09-15 09:55:01 UTC

Update Date

2021-09-14 15:46:46 UTC

HMDB ID

HMDB0010205

Secondary Accession Numbers

HMDB10205

Metabolite Identification

Common Name

14,15-EpETE

Description

14,15-EpETE, also known as 14(15)-epete, 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. Thus, 14,15-epete is considered to be an eicosanoid. Based on a literature review very few articles have been published on 14,15-EpETE.

Structure

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

HMDB0010205
     RDKit          3D
14,15-EpETE
 53 53  0  0  0  0  0  0  0  0999 V2000
   -8.5208    2.7451   -1.1436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4942    1.6282   -1.1494 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8201    0.5667   -0.1804 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0305    0.2426    0.8128 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7241    0.8660    1.1226 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5724   -0.1355    1.0818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3565    0.4824    1.3765 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5270    0.0221    0.0565 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6066   -1.1650   -0.2585 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8529   -1.5843    0.9205 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5610   -1.5968    1.0010 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3306   -1.1866   -0.1047 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2185   -2.3450   -0.4372 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5055   -2.2621   -0.3399 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2120   -1.0391    0.1018 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0967   -0.6455   -1.0297 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3881   -0.5625   -0.8826 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0949   -0.8307    0.3501 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8720    0.4163    0.8169 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8934    0.7846   -0.2248 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6394    1.9675    0.2484 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0310    3.0204    0.5343 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0136    1.9055    0.3771 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6661    3.1652   -0.1399 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2001    3.5242   -1.8604 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5104    2.3876   -1.4959 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5484    1.2210   -2.2098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4694    2.0045   -1.0611 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7571    0.0372   -0.3021 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3972   -0.5771    1.4672 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7837    1.1362    2.2306 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5078    1.8024    0.6262 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7850   -1.1451    1.4271 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7110    0.7553   -0.7424 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2526   -2.0284   -0.6295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0254   -0.8594   -1.1183 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4454   -1.9206    1.8224 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0395   -1.9307    1.9384 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2875   -0.9863   -1.0310 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8525   -0.2562    0.0793 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7186   -3.2806   -0.7731 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1598   -3.1221   -0.5857 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6040   -0.2032    0.4305 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7848   -1.3592    1.0141 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6204   -0.4210   -2.0145 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9727   -0.2671   -1.7799 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9398   -1.5444    0.0738 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5842   -1.2531    1.1973 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2098    1.2740    0.9613 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3514    0.1146    1.7644 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5960   -0.0152   -0.4531 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3744    1.0597   -1.1900 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.3887    1.3935    1.1669 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  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  2  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  2  0
 21 23  1  0
  8  6  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  2 27  1  0
  2 28  1  0
  3 29  1  0
  4 30  1  0
  5 31  1  0
  5 32  1  0
  6 33  1  0
  8 34  1  0
  9 35  1  0
  9 36  1  0
 10 37  1  0
 11 38  1  0
 12 39  1  0
 12 40  1  0
 13 41  1  0
 14 42  1  0
 15 43  1  0
 15 44  1  0
 16 45  1  0
 17 46  1  0
 18 47  1  0
 18 48  1  0
 19 49  1  0
 19 50  1  0
 20 51  1  0
 20 52  1  0
 23 53  1  0
M  END


  Mrv0541 02241200322D          

 23 23  0  0  0  0            999 V2000
   10.5984   -7.4765    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.8839   -7.0640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8839   -6.2390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5984   -5.8265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5984   -5.0015    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3129   -4.5890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3129   -3.7640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1695   -7.4765    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.5984   -3.3515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5984   -2.5265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8839   -2.1140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1695   -2.5265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4550   -2.1140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7405   -2.5265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7405   -3.3515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0261   -3.7640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6136   -4.4784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2011   -3.7640    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6136   -5.3034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8991   -5.7159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8991   -6.5409    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6136   -6.9534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6136   -7.7784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  2  0  0  0  0
  3  2  1  0  0  0  0
  4  3  1  0  0  0  0
  5  4  1  0  0  0  0
  6  5  1  0  0  0  0
  7  6  2  0  0  0  0
  8  2  1  0  0  0  0
  9  7  1  0  0  0  0
 10  9  1  0  0  0  0
 11 10  2  0  0  0  0
 12 11  1  0  0  0  0
 13 12  1  0  0  0  0
 14 13  2  0  0  0  0
 15 14  1  0  0  0  0
 16 15  1  0  0  0  0
 17 16  1  0  0  0  0
 18 16  1  0  0  0  0
 18 17  1  0  0  0  0
 19 17  1  0  0  0  0
 20 19  1  0  0  0  0
 21 20  2  0  0  0  0
 22 21  1  0  0  0  0
 23 22  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0010205

> <DATABASE_NAME>
hmdb

> <SMILES>
CC\C=C/CC1OC1C\C=C/C\C=C/C\C=C/CCCC(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C20H30O3/c1-2-3-12-15-18-19(23-18)16-13-10-8-6-4-5-7-9-11-14-17-20(21)22/h3-4,6-7,9-10,12-13,18-19H,2,5,8,11,14-17H2,1H3,(H,21,22)/b6-4-,9-7-,12-3-,13-10-

> <INCHI_KEY>
RGZIXZYRGZWDMI-QXBXTPPVSA-N

> <FORMULA>
C20H30O3

> <MOLECULAR_WEIGHT>
318.4504

> <EXACT_MASS>
318.219494826

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_AVERAGE_POLARIZABILITY>
37.52263895835014

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(5Z,8Z,11Z)-13-{3-[(2Z)-pent-2-en-1-yl]oxiran-2-yl}trideca-5,8,11-trienoic acid

> <ALOGPS_LOGP>
5.77

> <JCHEM_LOGP>
5.287252249333332

> <ALOGPS_LOGS>
-5.76

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.819771840930504

> <JCHEM_PKA_STRONGEST_BASIC>
-4.207091543676285

> <JCHEM_POLAR_SURFACE_AREA>
49.83

> <JCHEM_REFRACTIVITY>
99.4749

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.48e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(5Z,8Z,11Z)-13-{3-[(2Z)-pent-2-en-1-yl]oxiran-2-yl}trideca-5,8,11-trienoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0010205
     RDKit          3D
14,15-EpETE
 53 53  0  0  0  0  0  0  0  0999 V2000
   -8.5208    2.7451   -1.1436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4942    1.6282   -1.1494 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8201    0.5667   -0.1804 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0305    0.2426    0.8128 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7241    0.8660    1.1226 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5724   -0.1355    1.0818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3565    0.4824    1.3765 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5270    0.0221    0.0565 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6066   -1.1650   -0.2585 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8529   -1.5843    0.9205 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5610   -1.5968    1.0010 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3306   -1.1866   -0.1047 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2185   -2.3450   -0.4372 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5055   -2.2621   -0.3399 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2120   -1.0391    0.1018 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0967   -0.6455   -1.0297 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3881   -0.5625   -0.8826 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0949   -0.8307    0.3501 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8720    0.4163    0.8169 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8934    0.7846   -0.2248 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6394    1.9675    0.2484 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0310    3.0204    0.5343 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0136    1.9055    0.3771 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6661    3.1652   -0.1399 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2001    3.5242   -1.8604 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5104    2.3876   -1.4959 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5484    1.2210   -2.2098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4694    2.0045   -1.0611 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7571    0.0372   -0.3021 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3972   -0.5771    1.4672 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7837    1.1362    2.2306 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5078    1.8024    0.6262 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7850   -1.1451    1.4271 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7110    0.7553   -0.7424 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2526   -2.0284   -0.6295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0254   -0.8594   -1.1183 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4454   -1.9206    1.8224 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0395   -1.9307    1.9384 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2875   -0.9863   -1.0310 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8525   -0.2562    0.0793 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7186   -3.2806   -0.7731 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1598   -3.1221   -0.5857 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6040   -0.2032    0.4305 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7848   -1.3592    1.0141 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6204   -0.4210   -2.0145 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9727   -0.2671   -1.7799 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9398   -1.5444    0.0738 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5842   -1.2531    1.1973 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2098    1.2740    0.9613 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3514    0.1146    1.7644 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5960   -0.0152   -0.4531 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3744    1.0597   -1.1900 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.3887    1.3935    1.1669 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  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  2  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  2  0
 21 23  1  0
  8  6  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  2 27  1  0
  2 28  1  0
  3 29  1  0
  4 30  1  0
  5 31  1  0
  5 32  1  0
  6 33  1  0
  8 34  1  0
  9 35  1  0
  9 36  1  0
 10 37  1  0
 11 38  1  0
 12 39  1  0
 12 40  1  0
 13 41  1  0
 14 42  1  0
 15 43  1  0
 15 44  1  0
 16 45  1  0
 17 46  1  0
 18 47  1  0
 18 48  1  0
 19 49  1  0
 19 50  1  0
 20 51  1  0
 20 52  1  0
 23 53  1  0
M  END

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  O   UNK     0      19.784 -13.956   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      18.450 -13.186   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      18.450 -11.646   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      19.784 -10.876   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      19.784  -9.336   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      21.117  -8.566   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      21.117  -7.026   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      17.116 -13.956   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      19.784  -6.256   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      19.784  -4.716   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      18.450  -3.946   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      17.116  -4.716   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      15.783  -3.946   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      14.449  -4.716   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      14.449  -6.256   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      13.115  -7.026   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      12.345  -8.360   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      11.575  -7.026   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      12.345  -9.900   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      11.012 -10.670   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      11.012 -12.210   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      12.345 -12.980   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      12.345 -14.520   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    8                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    9                                                       
CONECT    8    2                                                            
CONECT    9    7   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   18                                                  
CONECT   17   16   18   19                                                  
CONECT   18   16   17                                                       
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   46    0
END

COMPND    HMDB0010205
HETATM    1  C1  UNL     1      -8.521   2.745  -1.144  1.00  0.00           C  
HETATM    2  C2  UNL     1      -7.494   1.628  -1.149  1.00  0.00           C  
HETATM    3  C3  UNL     1      -7.820   0.567  -0.180  1.00  0.00           C  
HETATM    4  C4  UNL     1      -7.030   0.243   0.813  1.00  0.00           C  
HETATM    5  C5  UNL     1      -5.724   0.866   1.123  1.00  0.00           C  
HETATM    6  C6  UNL     1      -4.572  -0.136   1.082  1.00  0.00           C  
HETATM    7  O1  UNL     1      -3.356   0.482   1.377  1.00  0.00           O  
HETATM    8  C7  UNL     1      -3.527   0.022   0.057  1.00  0.00           C  
HETATM    9  C8  UNL     1      -2.607  -1.165  -0.259  1.00  0.00           C  
HETATM   10  C9  UNL     1      -1.853  -1.584   0.920  1.00  0.00           C  
HETATM   11  C10 UNL     1      -0.561  -1.597   1.001  1.00  0.00           C  
HETATM   12  C11 UNL     1       0.331  -1.187  -0.105  1.00  0.00           C  
HETATM   13  C12 UNL     1       1.219  -2.345  -0.437  1.00  0.00           C  
HETATM   14  C13 UNL     1       2.505  -2.262  -0.340  1.00  0.00           C  
HETATM   15  C14 UNL     1       3.212  -1.039   0.102  1.00  0.00           C  
HETATM   16  C15 UNL     1       4.097  -0.645  -1.030  1.00  0.00           C  
HETATM   17  C16 UNL     1       5.388  -0.562  -0.883  1.00  0.00           C  
HETATM   18  C17 UNL     1       6.095  -0.831   0.350  1.00  0.00           C  
HETATM   19  C18 UNL     1       6.872   0.416   0.817  1.00  0.00           C  
HETATM   20  C19 UNL     1       7.893   0.785  -0.225  1.00  0.00           C  
HETATM   21  C20 UNL     1       8.639   1.968   0.248  1.00  0.00           C  
HETATM   22  O2  UNL     1       8.031   3.020   0.534  1.00  0.00           O  
HETATM   23  O3  UNL     1      10.014   1.905   0.377  1.00  0.00           O  
HETATM   24  H1  UNL     1      -8.666   3.165  -0.140  1.00  0.00           H  
HETATM   25  H2  UNL     1      -8.200   3.524  -1.860  1.00  0.00           H  
HETATM   26  H3  UNL     1      -9.510   2.388  -1.496  1.00  0.00           H  
HETATM   27  H4  UNL     1      -7.548   1.221  -2.210  1.00  0.00           H  
HETATM   28  H5  UNL     1      -6.469   2.005  -1.061  1.00  0.00           H  
HETATM   29  H6  UNL     1      -8.757   0.037  -0.302  1.00  0.00           H  
HETATM   30  H7  UNL     1      -7.397  -0.577   1.467  1.00  0.00           H  
HETATM   31  H8  UNL     1      -5.784   1.136   2.231  1.00  0.00           H  
HETATM   32  H9  UNL     1      -5.508   1.802   0.626  1.00  0.00           H  
HETATM   33  H10 UNL     1      -4.785  -1.145   1.427  1.00  0.00           H  
HETATM   34  H11 UNL     1      -3.711   0.755  -0.742  1.00  0.00           H  
HETATM   35  H12 UNL     1      -3.253  -2.028  -0.629  1.00  0.00           H  
HETATM   36  H13 UNL     1      -2.025  -0.859  -1.118  1.00  0.00           H  
HETATM   37  H14 UNL     1      -2.445  -1.921   1.822  1.00  0.00           H  
HETATM   38  H15 UNL     1      -0.039  -1.931   1.938  1.00  0.00           H  
HETATM   39  H16 UNL     1      -0.287  -0.986  -1.031  1.00  0.00           H  
HETATM   40  H17 UNL     1       0.853  -0.256   0.079  1.00  0.00           H  
HETATM   41  H18 UNL     1       0.719  -3.281  -0.773  1.00  0.00           H  
HETATM   42  H19 UNL     1       3.160  -3.122  -0.586  1.00  0.00           H  
HETATM   43  H20 UNL     1       2.604  -0.203   0.431  1.00  0.00           H  
HETATM   44  H21 UNL     1       3.785  -1.359   1.014  1.00  0.00           H  
HETATM   45  H22 UNL     1       3.620  -0.421  -2.014  1.00  0.00           H  
HETATM   46  H23 UNL     1       5.973  -0.267  -1.780  1.00  0.00           H  
HETATM   47  H24 UNL     1       6.940  -1.544   0.074  1.00  0.00           H  
HETATM   48  H25 UNL     1       5.584  -1.253   1.197  1.00  0.00           H  
HETATM   49  H26 UNL     1       6.210   1.274   0.961  1.00  0.00           H  
HETATM   50  H27 UNL     1       7.351   0.115   1.764  1.00  0.00           H  
HETATM   51  H28 UNL     1       8.596  -0.015  -0.453  1.00  0.00           H  
HETATM   52  H29 UNL     1       7.374   1.060  -1.190  1.00  0.00           H  
HETATM   53  H30 UNL     1      10.389   1.393   1.167  1.00  0.00           H  
CONECT    1    2   24   25   26
CONECT    2    3   27   28
CONECT    3    4    4   29
CONECT    4    5   30
CONECT    5    6   31   32
CONECT    6    7    8   33
CONECT    7    8
CONECT    8    9   34
CONECT    9   10   35   36
CONECT   10   11   11   37
CONECT   11   12   38
CONECT   12   13   39   40
CONECT   13   14   14   41
CONECT   14   15   42
CONECT   15   16   43   44
CONECT   16   17   17   45
CONECT   17   18   46
CONECT   18   19   47   48
CONECT   19   20   49   50
CONECT   20   21   51   52
CONECT   21   22   22   23
CONECT   23   53
END

HMDB0010205
     RDKit          3D
14,15-EpETE
 53 53  0  0  0  0  0  0  0  0999 V2000
   -8.5208    2.7451   -1.1436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4942    1.6282   -1.1494 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8201    0.5667   -0.1804 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0305    0.2426    0.8128 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7241    0.8660    1.1226 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5724   -0.1355    1.0818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3565    0.4824    1.3765 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5270    0.0221    0.0565 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6066   -1.1650   -0.2585 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8529   -1.5843    0.9205 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5610   -1.5968    1.0010 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3306   -1.1866   -0.1047 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2185   -2.3450   -0.4372 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5055   -2.2621   -0.3399 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2120   -1.0391    0.1018 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0967   -0.6455   -1.0297 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3881   -0.5625   -0.8826 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0949   -0.8307    0.3501 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8720    0.4163    0.8169 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8934    0.7846   -0.2248 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6394    1.9675    0.2484 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0310    3.0204    0.5343 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0136    1.9055    0.3771 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6661    3.1652   -0.1399 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2001    3.5242   -1.8604 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5104    2.3876   -1.4959 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5484    1.2210   -2.2098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4694    2.0045   -1.0611 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7571    0.0372   -0.3021 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3972   -0.5771    1.4672 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7837    1.1362    2.2306 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5078    1.8024    0.6262 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7850   -1.1451    1.4271 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7110    0.7553   -0.7424 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2526   -2.0284   -0.6295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0254   -0.8594   -1.1183 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4454   -1.9206    1.8224 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0395   -1.9307    1.9384 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2875   -0.9863   -1.0310 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8525   -0.2562    0.0793 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7186   -3.2806   -0.7731 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1598   -3.1221   -0.5857 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6040   -0.2032    0.4305 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7848   -1.3592    1.0141 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6204   -0.4210   -2.0145 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9727   -0.2671   -1.7799 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9398   -1.5444    0.0738 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5842   -1.2531    1.1973 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2098    1.2740    0.9613 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3514    0.1146    1.7644 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5960   -0.0152   -0.4531 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3744    1.0597   -1.1900 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.3887    1.3935    1.1669 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  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  2  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  2  0
 21 23  1  0
  8  6  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  2 27  1  0
  2 28  1  0
  3 29  1  0
  4 30  1  0
  5 31  1  0
  5 32  1  0
  6 33  1  0
  8 34  1  0
  9 35  1  0
  9 36  1  0
 10 37  1  0
 11 38  1  0
 12 39  1  0
 12 40  1  0
 13 41  1  0
 14 42  1  0
 15 43  1  0
 15 44  1  0
 16 45  1  0
 17 46  1  0
 18 47  1  0
 18 48  1  0
 19 49  1  0
 19 50  1  0
 20 51  1  0
 20 52  1  0
 23 53  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
14(15)-EpETE	ChEBI
14(15)-Epoxy-5Z,8Z,11Z,17Z-eicosatetraenoic acid	ChEBI
14,15-Epoxy-(5Z,8Z,11Z,17Z)-eicosatetraenoic acid	ChEBI
14,15-Epoxy-(5Z,8Z,11Z,17Z)-icosatetraenoic acid	ChEBI
14(15)-Epoxy-5Z,8Z,11Z,17Z-eicosatetraenoate	Generator
14,15-Epoxy-(5Z,8Z,11Z,17Z)-eicosatetraenoate	Generator
14,15-Epoxy-(5Z,8Z,11Z,17Z)-icosatetraenoate	Generator
(+/-)-14(15)-epoxy-5Z,8Z,11Z,17Z-eicosatetraenoate	HMDB
(+/-)-14(15)-epoxy-5Z,8Z,11Z,17Z-eicosatetraenoic acid	HMDB
(5Z,8Z,11Z)-13-[3-[(Z)-Pent-2-enyl]oxiran-2-yl]trideca-5,8,11-trienoate	HMDB
(5Z,8Z,11Z)-13-[3-[(Z)-Pent-2-enyl]oxiran-2-yl]trideca-5,8,11-trienoic acid	HMDB
(5Z,8Z,11Z,17Z)-14,15-Epoxyicosatetraenoate	HMDB

Chemical Formula

C₂₀H₃₀O₃

Average Molecular Weight

318.4504

Monoisotopic Molecular Weight

318.219494826

IUPAC Name

(5Z,8Z,11Z)-13-{3-[(2Z)-pent-2-en-1-yl]oxiran-2-yl}trideca-5,8,11-trienoic acid

Traditional Name

(5Z,8Z,11Z)-13-{3-[(2Z)-pent-2-en-1-yl]oxiran-2-yl}trideca-5,8,11-trienoic acid

CAS Registry Number

Not Available

SMILES

CC\C=C/CC1OC1C\C=C/C\C=C/C\C=C/CCCC(O)=O

InChI Identifier

InChI=1S/C20H30O3/c1-2-3-12-15-18-19(23-18)16-13-10-8-6-4-5-7-9-11-14-17-20(21)22/h3-4,6-7,9-10,12-13,18-19H,2,5,8,11,14-17H2,1H3,(H,21,22)/b6-4-,9-7-,12-3-,13-10-

InChI Key

RGZIXZYRGZWDMI-QXBXTPPVSA-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
Epoxy fatty acid
Heterocyclic fatty acid
Unsaturated fatty acid
Carboxylic acid derivative
Carboxylic acid
Dialkyl ether
Oxirane
Ether
Monocarboxylic acid or derivatives
Organoheterocyclic compound
Oxacycle
Organic oxide
Hydrocarbon derivative
Carbonyl group
Organooxygen compound
Organic oxygen compound
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

Other Eicosanoids (LMFA03000003 )

Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 18953024)

Cellular substructure

Membrane (HMDB: HMDB0010205)

Source

Endogenous

Endogenous (HMDB: HMDB0010205)

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)
Greylag goose (FooDB: FOOD00368)
Guinea hen (FooDB: FOOD00373)
Ostrich (FooDB: FOOD00422)
Velvet duck (FooDB: FOOD00427)

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)

Equine

Horse (FooDB: FOOD00378)

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

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.00055 g/L	ALOGPS
logP	5.77	ALOGPS
logP	5.29	ChemAxon
logS	-5.8	ALOGPS
pKa (Strongest Acidic)	4.82	ChemAxon
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	49.83 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	99.47 m³·mol⁻¹	ChemAxon
Polarizability	37.52 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	185.19	31661259
DarkChem	[M-H]-	184.036	31661259
DeepCCS	[M+H]+	182.905	30932474
DeepCCS	[M-H]-	180.547	30932474
DeepCCS	[M-2H]-	213.433	30932474
DeepCCS	[M+Na]+	188.998	30932474
AllCCS	[M+H]+	187.2	32859911
AllCCS	[M+H-H2O]+	184.3	32859911
AllCCS	[M+NH4]+	190.0	32859911
AllCCS	[M+Na]+	190.7	32859911
AllCCS	[M-H]-	185.5	32859911
AllCCS	[M+Na-2H]-	187.0	32859911
AllCCS	[M+HCOO]-	188.7	32859911

Predicted Retention Times

Underivatized

Chromatographic Method	Retention Time	Reference
Measured using a Waters Acquity ultraperformance liquid chromatography (UPLC) ethylene-bridged hybrid (BEH) C18 column (100 mm × 2.1 mm; 1.7 μmparticle diameter). Predicted by Afia on May 17, 2022.	7.01 minutes	32390414
Predicted by Siyang on May 30, 2022	22.4603 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	0.9 minutes	32390414
AjsUoB = Accucore 150 Amide HILIC with 10mM Ammonium Formate, 0.1% Formic Acid	33.1 seconds	40023050
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	3098.3 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	500.0 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	218.3 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	355.6 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	647.4 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	1091.5 seconds	40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid	540.4 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	91.1 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	2102.9 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	720.8 seconds	40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid	1819.8 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	794.1 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	513.0 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	421.5 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	550.9 seconds	40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water	8.6 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
14,15-EpETE	CC\C=C/CC1OC1C\C=C/C\C=C/C\C=C/CCCC(O)=O	3783.3	Standard polar	33892256
14,15-EpETE	CC\C=C/CC1OC1C\C=C/C\C=C/C\C=C/CCCC(O)=O	2295.7	Standard non polar	33892256
14,15-EpETE	CC\C=C/CC1OC1C\C=C/C\C=C/C\C=C/CCCC(O)=O	2501.1	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
14,15-EpETE,1TMS,isomer #1	CC/C=C\CC1OC1C/C=C\C/C=C\C/C=C\CCCC(=O)O[Si](C)(C)C	2465.6	Semi standard non polar	33892256
14,15-EpETE,1TBDMS,isomer #1	CC/C=C\CC1OC1C/C=C\C/C=C\C/C=C\CCCC(=O)O[Si](C)(C)C(C)(C)C	2715.1	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 14,15-EpETE GC-MS (Non-derivatized) - 70eV, Positive	splash10-00kf-6390000000-8bca9904b8100bd4fcc5	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 14,15-EpETE GC-MS (1 TMS) - 70eV, Positive	splash10-00b9-9272000000-b95aa46c3e4dda452b53	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 14,15-EpETE 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 - 14,15-EpETE 10V, Positive-QTOF	splash10-0udi-1139000000-02dd0f3a11a425276020	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 14,15-EpETE 20V, Positive-QTOF	splash10-0f8i-9662000000-5e02c3ecfe41c9920da7	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 14,15-EpETE 40V, Positive-QTOF	splash10-0mkv-9800000000-85e19b799db4cc4fb961	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 14,15-EpETE 10V, Negative-QTOF	splash10-014i-1059000000-9bdac78c4ac5f04c5d4b	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 14,15-EpETE 20V, Negative-QTOF	splash10-014j-3194000000-ec0e9a77eba78b15b617	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 14,15-EpETE 40V, Negative-QTOF	splash10-052f-9120000000-e3708dd5177e52369a62	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 14,15-EpETE 10V, Negative-QTOF	splash10-014i-0239000000-811f153940cca99e91a7	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 14,15-EpETE 20V, Negative-QTOF	splash10-00kb-2294000000-d09ef5637ab257890322	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 14,15-EpETE 40V, Negative-QTOF	splash10-0006-9230000000-63b7cdb38338cb431814	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 14,15-EpETE 10V, Positive-QTOF	splash10-0uyi-3269000000-37c784c17737cc91e90a	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 14,15-EpETE 20V, Positive-QTOF	splash10-0f8c-9633000000-1a3f4242ef760f535b67	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 14,15-EpETE 40V, Positive-QTOF	splash10-05ox-9400000000-b7c207171392d16771e3	2021-09-22	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Membrane (predicted from logP)

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	0.000242 +/- 0.000101 uM	Adult (>18 years old)	Not Specified	Normal	18953024	details
Blood	Detected and Quantified	0.000119 +/- 0.000029 uM	Adult (>18 years old)	Both	Normal	21359215	details
Blood	Detected and Quantified	<0.0001 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

FDB027360

KNApSAcK ID

Not Available

Chemspider ID

17220771

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

16061088

PDB ID

Not Available

ChEBI ID

137269

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

Barbosa-Sicard E, Markovic M, Honeck H, Christ B, Muller DN, Schunck WH: Eicosapentaenoic acid metabolism by cytochrome P450 enzymes of the CYP2C subfamily. Biochem Biophys Res Commun. 2005 Apr 22;329(4):1275-81. [PubMed:15766564 ]

Showing metabocard for 14,15-EpETE (HMDB0010205)

MOL for HMDB0010205 (14,15-EpETE)

3D MOL for HMDB0010205 (14,15-EpETE)

3D SDF for HMDB0010205 (14,15-EpETE)

3D-SDF for HMDB0010205 (14,15-EpETE)

PDB for HMDB0010205 (14,15-EpETE)

3D PDB for HMDB0010205 (14,15-EpETE)

SMILES for HMDB0010205 (14,15-EpETE)

INCHI for HMDB0010205 (14,15-EpETE)

Structure for HMDB0010205 (14,15-EpETE)

3D Structure for HMDB0010205 (14,15-EpETE)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra