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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2017-03-23 05:31:03 UTC

Update Date

2022-03-07 03:17:58 UTC

HMDB ID

HMDB0062688

Secondary Accession Numbers

HMDB62688

Metabolite Identification

Common Name

15-HPETE

Description

15-HPETE belongs to the class of organic compounds known as hydroperoxyeicosatetraenoic acids. These are eicosanoic acids with an attached hydroperoxyl group and four CC double bonds. Thus, 15-hpete is considered to be an eicosanoid lipid molecule. 15-HPETE is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral.

Structure

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

  Mrv1652303231706312D          

 32 31  0  0  0  0            999 V2000
    1.2375   -7.8592    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250   -7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125   -7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2375   -7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6500   -8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4750   -8.5737    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2375   -9.2881    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375   -6.4302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625   -6.4302    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250   -5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375   -5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250   -4.2868    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625   -5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4750   -4.2868    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4750   -5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000   -5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7125   -6.4302    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7125   -5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375   -5.0013    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000   -4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8875   -5.0013    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7125   -3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375   -3.5724    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4750   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625   -2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375   -2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250   -1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7125   -2.1434    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375   -2.1434    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  2  0  0  0  0
  2  9  2  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  2  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 25 31  1  0  0  0  0
 31 32  1  0  0  0  0
M  END

HMDB0062688
     RDKit          3D
15-HPETE
 56 55  0  0  0  0  0  0  0  0999 V2000
   -8.4074    0.4197   -1.0398 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3787   -0.2807   -0.1650 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6158    0.7744    0.5654 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5511    0.2386    1.4787 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5113   -0.5671    0.7626 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4975   -1.0442    1.7998 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4325   -1.8427    1.1912 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3431   -1.3188    0.6024 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2022    0.1295    0.5608 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1783    0.7358    0.0060 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9164    0.0020   -0.6258 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1212    0.3455   -2.0332 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1975    0.8828   -2.4986 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3960    1.2673   -1.7986 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5861    1.1542   -0.3861 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5033    0.4401    0.2138 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5252   -0.3908   -0.4106 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9355    0.0933   -0.0227 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9192   -0.8254   -0.7198 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3009   -0.3729   -0.3576 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7637   -0.6652    0.7527 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0341    0.3604   -1.2635 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1741   -1.8084    2.7708 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1563   -1.2112    3.9238 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4361    0.2309   -0.6793 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3618    0.0215   -2.0933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2240    1.5141   -1.0826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9163   -0.8948    0.5960 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7515   -0.9153   -0.8057 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2427    1.5422   -0.1268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3603    1.3109    1.2223 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0230    1.1167    1.9210 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9977   -0.3324    2.3146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9307   -1.4661    0.2596 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9846    0.0072   -0.0191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1406   -0.1415    2.3291 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5368   -2.9161    1.2212 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6484   -2.0301    0.2095 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9765    0.7709    1.0077 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1306    1.8276    0.0099 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5025   -1.0920   -0.7153 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7753   -0.1781    0.0089 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2537    0.1100   -2.7079 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1487    1.0602   -3.6260 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2433    0.6814   -2.3029 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7300    2.3386   -2.1470 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9252    1.7399    0.2989 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5193    0.4581    1.3253 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5005   -1.4550   -0.0057 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5451   -0.4437   -1.5018 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0278    1.1325   -0.4128 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0548    0.0147    1.0621 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7311   -1.8585   -0.3972 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7872   -0.7920   -1.8229 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.0121    1.3737   -1.3217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8458   -1.7935    4.6751 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  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
  6 23  1  0
 23 24  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  2 28  1  0
  2 29  1  0
  3 30  1  0
  3 31  1  0
  4 32  1  0
  4 33  1  0
  5 34  1  0
  5 35  1  0
  6 36  1  0
  7 37  1  0
  8 38  1  0
  9 39  1  0
 10 40  1  0
 11 41  1  0
 11 42  1  0
 12 43  1  0
 13 44  1  0
 14 45  1  0
 14 46  1  0
 15 47  1  0
 16 48  1  0
 17 49  1  0
 17 50  1  0
 18 51  1  0
 18 52  1  0
 19 53  1  0
 19 54  1  0
 22 55  1  0
 24 56  1  0
M  END

  Mrv1652303231706312D          

 32 31  0  0  0  0            999 V2000
    1.2375   -7.8592    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250   -7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125   -7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2375   -7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6500   -8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4750   -8.5737    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2375   -9.2881    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375   -6.4302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625   -6.4302    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250   -5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375   -5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250   -4.2868    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625   -5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4750   -4.2868    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4750   -5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000   -5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7125   -6.4302    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7125   -5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375   -5.0013    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000   -4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8875   -5.0013    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7125   -3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375   -3.5724    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4750   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625   -2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375   -2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250   -1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7125   -2.1434    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375   -2.1434    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  2  0  0  0  0
  2  9  2  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  2  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 25 31  1  0  0  0  0
 31 32  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0062688

> <DATABASE_NAME>
hmdb

> <SMILES>
[H]\C(CCCC(O)=O)=C(/[H])C\C([H])=C(\[H])C\C([H])=C(\[H])C([H])=C([H])C(CCCCC)OO

> <INCHI_IDENTIFIER>
InChI=1S/C20H32O4/c1-2-3-13-16-19(24-23)17-14-11-9-7-5-4-6-8-10-12-15-18-20(21)22/h4-5,8-11,14,17,19,23H,2-3,6-7,12-13,15-16,18H2,1H3,(H,21,22)/b5-4-,10-8-,11-9-,17-14+

> <INCHI_KEY>
BFWYTORDSFIVKP-USWFWKISSA-N

> <FORMULA>
C20H32O4

> <MOLECULAR_WEIGHT>
336.472

> <EXACT_MASS>
336.23005951

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
39.59402052995182

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(5Z,8Z,11Z,13E)-15-hydroperoxyicosa-5,8,11,13-tetraenoic acid

> <ALOGPS_LOGP>
5.86

> <JCHEM_LOGP>
5.805695121333333

> <ALOGPS_LOGS>
-5.27

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
11.712374063193028

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.819771784961381

> <JCHEM_PKA_STRONGEST_BASIC>
-4.236807609084836

> <JCHEM_POLAR_SURFACE_AREA>
66.76

> <JCHEM_REFRACTIVITY>
102.81969999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
15

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.80e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(5Z,8Z,11Z,13E)-15-hydroperoxyicosa-5,8,11,13-tetraenoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0062688
     RDKit          3D
15-HPETE
 56 55  0  0  0  0  0  0  0  0999 V2000
   -8.4074    0.4197   -1.0398 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3787   -0.2807   -0.1650 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6158    0.7744    0.5654 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5511    0.2386    1.4787 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5113   -0.5671    0.7626 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4975   -1.0442    1.7998 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4325   -1.8427    1.1912 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3431   -1.3188    0.6024 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2022    0.1295    0.5608 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1783    0.7358    0.0060 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9164    0.0020   -0.6258 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1212    0.3455   -2.0332 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1975    0.8828   -2.4986 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3960    1.2673   -1.7986 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5861    1.1542   -0.3861 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5033    0.4401    0.2138 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5252   -0.3908   -0.4106 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9355    0.0933   -0.0227 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9192   -0.8254   -0.7198 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3009   -0.3729   -0.3576 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7637   -0.6652    0.7527 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0341    0.3604   -1.2635 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1741   -1.8084    2.7708 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1563   -1.2112    3.9238 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4361    0.2309   -0.6793 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3618    0.0215   -2.0933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2240    1.5141   -1.0826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9163   -0.8948    0.5960 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7515   -0.9153   -0.8057 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2427    1.5422   -0.1268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3603    1.3109    1.2223 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0230    1.1167    1.9210 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9977   -0.3324    2.3146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9307   -1.4661    0.2596 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9846    0.0072   -0.0191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1406   -0.1415    2.3291 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5368   -2.9161    1.2212 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6484   -2.0301    0.2095 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9765    0.7709    1.0077 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1306    1.8276    0.0099 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5025   -1.0920   -0.7153 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7753   -0.1781    0.0089 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2537    0.1100   -2.7079 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1487    1.0602   -3.6260 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2433    0.6814   -2.3029 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7300    2.3386   -2.1470 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9252    1.7399    0.2989 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5193    0.4581    1.3253 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5005   -1.4550   -0.0057 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5451   -0.4437   -1.5018 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0278    1.1325   -0.4128 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0548    0.0147    1.0621 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7311   -1.8585   -0.3972 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7872   -0.7920   -1.8229 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.0121    1.3737   -1.3217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8458   -1.7935    4.6751 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  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
  6 23  1  0
 23 24  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  2 28  1  0
  2 29  1  0
  3 30  1  0
  3 31  1  0
  4 32  1  0
  4 33  1  0
  5 34  1  0
  5 35  1  0
  6 36  1  0
  7 37  1  0
  8 38  1  0
  9 39  1  0
 10 40  1  0
 11 41  1  0
 11 42  1  0
 12 43  1  0
 13 44  1  0
 14 45  1  0
 14 46  1  0
 15 47  1  0
 16 48  1  0
 17 49  1  0
 17 50  1  0
 18 51  1  0
 18 52  1  0
 19 53  1  0
 19 54  1  0
 22 55  1  0
 24 56  1  0
M  END

HEADER    PROTEIN                                 23-MAR-17   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-MAR-17         0                                  
HETATM    1  H   UNK     0       2.310 -14.670   0.000  0.00  0.00           H+0
HETATM    2  C   UNK     0       1.540 -13.337   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.000 -13.337   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.770 -14.670   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.310 -14.670   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -3.080 -16.004   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -4.620 -16.004   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0      -2.310 -17.338   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       2.310 -12.003   0.000  0.00  0.00           C+0
HETATM   10  H   UNK     0       3.850 -12.003   0.000  0.00  0.00           H+0
HETATM   11  C   UNK     0       1.540 -10.669   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.310  -9.336   0.000  0.00  0.00           C+0
HETATM   13  H   UNK     0       1.540  -8.002   0.000  0.00  0.00           H+0
HETATM   14  C   UNK     0       3.850  -9.336   0.000  0.00  0.00           C+0
HETATM   15  H   UNK     0       4.620  -8.002   0.000  0.00  0.00           H+0
HETATM   16  C   UNK     0       4.620 -10.669   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.160 -10.669   0.000  0.00  0.00           C+0
HETATM   18  H   UNK     0       6.930 -12.003   0.000  0.00  0.00           H+0
HETATM   19  C   UNK     0       6.930  -9.336   0.000  0.00  0.00           C+0
HETATM   20  H   UNK     0       8.470  -9.336   0.000  0.00  0.00           H+0
HETATM   21  C   UNK     0       6.160  -8.002   0.000  0.00  0.00           C+0
HETATM   22  H   UNK     0       5.390  -9.336   0.000  0.00  0.00           H+0
HETATM   23  C   UNK     0       6.930  -6.668   0.000  0.00  0.00           C+0
HETATM   24  H   UNK     0       8.470  -6.668   0.000  0.00  0.00           H+0
HETATM   25  C   UNK     0       6.160  -5.335   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.620  -5.335   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       3.850  -4.001   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.310  -4.001   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       1.540  -2.667   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       0.000  -2.667   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       6.930  -4.001   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       8.470  -4.001   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    9                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6                                                            
CONECT    9    2   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   31                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29                                                            
CONECT   31   25   32                                                       
CONECT   32   31                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   62    0
END

COMPND    HMDB0062688
HETATM    1  C1  UNL     1      -8.407   0.420  -1.040  1.00  0.00           C  
HETATM    2  C2  UNL     1      -7.379  -0.281  -0.165  1.00  0.00           C  
HETATM    3  C3  UNL     1      -6.616   0.774   0.565  1.00  0.00           C  
HETATM    4  C4  UNL     1      -5.551   0.239   1.479  1.00  0.00           C  
HETATM    5  C5  UNL     1      -4.511  -0.567   0.763  1.00  0.00           C  
HETATM    6  C6  UNL     1      -3.497  -1.044   1.800  1.00  0.00           C  
HETATM    7  C7  UNL     1      -2.432  -1.843   1.191  1.00  0.00           C  
HETATM    8  C8  UNL     1      -1.343  -1.319   0.602  1.00  0.00           C  
HETATM    9  C9  UNL     1      -1.202   0.130   0.561  1.00  0.00           C  
HETATM   10  C10 UNL     1      -0.178   0.736   0.006  1.00  0.00           C  
HETATM   11  C11 UNL     1       0.916   0.002  -0.626  1.00  0.00           C  
HETATM   12  C12 UNL     1       1.121   0.345  -2.033  1.00  0.00           C  
HETATM   13  C13 UNL     1       2.197   0.883  -2.499  1.00  0.00           C  
HETATM   14  C14 UNL     1       3.396   1.267  -1.799  1.00  0.00           C  
HETATM   15  C15 UNL     1       3.586   1.154  -0.386  1.00  0.00           C  
HETATM   16  C16 UNL     1       4.503   0.440   0.214  1.00  0.00           C  
HETATM   17  C17 UNL     1       5.525  -0.391  -0.411  1.00  0.00           C  
HETATM   18  C18 UNL     1       6.936   0.093  -0.023  1.00  0.00           C  
HETATM   19  C19 UNL     1       7.919  -0.825  -0.720  1.00  0.00           C  
HETATM   20  C20 UNL     1       9.301  -0.373  -0.358  1.00  0.00           C  
HETATM   21  O1  UNL     1       9.764  -0.665   0.753  1.00  0.00           O  
HETATM   22  O2  UNL     1      10.034   0.360  -1.263  1.00  0.00           O  
HETATM   23  O3  UNL     1      -4.174  -1.808   2.771  1.00  0.00           O  
HETATM   24  O4  UNL     1      -4.156  -1.211   3.924  1.00  0.00           O  
HETATM   25  H1  UNL     1      -9.436   0.231  -0.679  1.00  0.00           H  
HETATM   26  H2  UNL     1      -8.362   0.021  -2.093  1.00  0.00           H  
HETATM   27  H3  UNL     1      -8.224   1.514  -1.083  1.00  0.00           H  
HETATM   28  H4  UNL     1      -7.916  -0.895   0.596  1.00  0.00           H  
HETATM   29  H5  UNL     1      -6.752  -0.915  -0.806  1.00  0.00           H  
HETATM   30  H6  UNL     1      -6.243   1.542  -0.127  1.00  0.00           H  
HETATM   31  H7  UNL     1      -7.360   1.311   1.222  1.00  0.00           H  
HETATM   32  H8  UNL     1      -5.023   1.117   1.921  1.00  0.00           H  
HETATM   33  H9  UNL     1      -5.998  -0.332   2.315  1.00  0.00           H  
HETATM   34  H10 UNL     1      -4.931  -1.466   0.260  1.00  0.00           H  
HETATM   35  H11 UNL     1      -3.985   0.007  -0.019  1.00  0.00           H  
HETATM   36  H12 UNL     1      -3.141  -0.141   2.329  1.00  0.00           H  
HETATM   37  H13 UNL     1      -2.537  -2.916   1.221  1.00  0.00           H  
HETATM   38  H14 UNL     1      -0.648  -2.030   0.210  1.00  0.00           H  
HETATM   39  H15 UNL     1      -1.977   0.771   1.008  1.00  0.00           H  
HETATM   40  H16 UNL     1      -0.131   1.828   0.010  1.00  0.00           H  
HETATM   41  H17 UNL     1       0.502  -1.092  -0.715  1.00  0.00           H  
HETATM   42  H18 UNL     1       1.775  -0.178   0.009  1.00  0.00           H  
HETATM   43  H19 UNL     1       0.254   0.110  -2.708  1.00  0.00           H  
HETATM   44  H20 UNL     1       2.149   1.060  -3.626  1.00  0.00           H  
HETATM   45  H21 UNL     1       4.243   0.681  -2.303  1.00  0.00           H  
HETATM   46  H22 UNL     1       3.730   2.339  -2.147  1.00  0.00           H  
HETATM   47  H23 UNL     1       2.925   1.740   0.299  1.00  0.00           H  
HETATM   48  H24 UNL     1       4.519   0.458   1.325  1.00  0.00           H  
HETATM   49  H25 UNL     1       5.500  -1.455  -0.006  1.00  0.00           H  
HETATM   50  H26 UNL     1       5.545  -0.444  -1.502  1.00  0.00           H  
HETATM   51  H27 UNL     1       7.028   1.133  -0.413  1.00  0.00           H  
HETATM   52  H28 UNL     1       7.055   0.015   1.062  1.00  0.00           H  
HETATM   53  H29 UNL     1       7.731  -1.858  -0.397  1.00  0.00           H  
HETATM   54  H30 UNL     1       7.787  -0.792  -1.823  1.00  0.00           H  
HETATM   55  H31 UNL     1      10.012   1.374  -1.322  1.00  0.00           H  
HETATM   56  H32 UNL     1      -3.846  -1.793   4.675  1.00  0.00           H  
CONECT    1    2   25   26   27
CONECT    2    3   28   29
CONECT    3    4   30   31
CONECT    4    5   32   33
CONECT    5    6   34   35
CONECT    6    7   23   36
CONECT    7    8    8   37
CONECT    8    9   38
CONECT    9   10   10   39
CONECT   10   11   40
CONECT   11   12   41   42
CONECT   12   13   13   43
CONECT   13   14   44
CONECT   14   15   45   46
CONECT   15   16   16   47
CONECT   16   17   48
CONECT   17   18   49   50
CONECT   18   19   51   52
CONECT   19   20   53   54
CONECT   20   21   21   22
CONECT   22   55
CONECT   23   24
CONECT   24   56
END

HMDB0062688
     RDKit          3D
15-HPETE
 56 55  0  0  0  0  0  0  0  0999 V2000
   -8.4074    0.4197   -1.0398 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3787   -0.2807   -0.1650 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6158    0.7744    0.5654 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5511    0.2386    1.4787 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5113   -0.5671    0.7626 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4975   -1.0442    1.7998 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4325   -1.8427    1.1912 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3431   -1.3188    0.6024 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2022    0.1295    0.5608 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1783    0.7358    0.0060 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9164    0.0020   -0.6258 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1212    0.3455   -2.0332 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1975    0.8828   -2.4986 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3960    1.2673   -1.7986 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5861    1.1542   -0.3861 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5033    0.4401    0.2138 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5252   -0.3908   -0.4106 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9355    0.0933   -0.0227 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9192   -0.8254   -0.7198 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3009   -0.3729   -0.3576 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7637   -0.6652    0.7527 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0341    0.3604   -1.2635 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1741   -1.8084    2.7708 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1563   -1.2112    3.9238 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4361    0.2309   -0.6793 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3618    0.0215   -2.0933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2240    1.5141   -1.0826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9163   -0.8948    0.5960 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7515   -0.9153   -0.8057 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2427    1.5422   -0.1268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3603    1.3109    1.2223 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0230    1.1167    1.9210 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9977   -0.3324    2.3146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9307   -1.4661    0.2596 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9846    0.0072   -0.0191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1406   -0.1415    2.3291 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5368   -2.9161    1.2212 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6484   -2.0301    0.2095 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9765    0.7709    1.0077 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1306    1.8276    0.0099 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5025   -1.0920   -0.7153 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7753   -0.1781    0.0089 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2537    0.1100   -2.7079 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1487    1.0602   -3.6260 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2433    0.6814   -2.3029 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7300    2.3386   -2.1470 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9252    1.7399    0.2989 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5193    0.4581    1.3253 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5005   -1.4550   -0.0057 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5451   -0.4437   -1.5018 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0278    1.1325   -0.4128 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0548    0.0147    1.0621 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7311   -1.8585   -0.3972 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7872   -0.7920   -1.8229 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.0121    1.3737   -1.3217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8458   -1.7935    4.6751 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  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
  6 23  1  0
 23 24  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  2 28  1  0
  2 29  1  0
  3 30  1  0
  3 31  1  0
  4 32  1  0
  4 33  1  0
  5 34  1  0
  5 35  1  0
  6 36  1  0
  7 37  1  0
  8 38  1  0
  9 39  1  0
 10 40  1  0
 11 41  1  0
 11 42  1  0
 12 43  1  0
 13 44  1  0
 14 45  1  0
 14 46  1  0
 15 47  1  0
 16 48  1  0
 17 49  1  0
 17 50  1  0
 18 51  1  0
 18 52  1  0
 19 53  1  0
 19 54  1  0
 22 55  1  0
 24 56  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
(6E,8Z,11Z,14Z)-15-Hydroperoxyicosatetraenoic acid	ChEBI
15-Hydroperoxy-(5Z,8Z,11Z,13E)-eicosatetraenoic acid	ChEBI
15-Hydroperoxy-(5Z,8Z,11Z,13E)-icosatetraenoic acid	ChEBI
15-Hydroperoxy-5,8,11,13-eicosatetraenoic acid	ChEBI
(6E,8Z,11Z,14Z)-15-Hydroperoxyicosatetraenoate	Generator
15-Hydroperoxy-(5Z,8Z,11Z,13E)-eicosatetraenoate	Generator
15-Hydroperoxy-(5Z,8Z,11Z,13E)-icosatetraenoate	Generator
15-Hydroperoxy-5,8,11,13-eicosatetraenoate	Generator
14,15-Epoxyarachidonic acid	HMDB
15-HPAA	HMDB
15-HPEA	HMDB
15-Hydroperoxy-5,8,11,13-eicosatetraenoic acid, (e,Z,Z,Z)-isomer	HMDB
15-Hydroperoxy-5,8,11,13-eicosatetraenoic acid, (S)-(e,Z,Z,Z)-isomer	HMDB
15-Hydroperoxy-5,8,11,13-eicosatetraenoic acid, (Z,Z,Z,Z)-isomer	HMDB
15-Hydroperoxy-5,8,11,14-eicosatetraenoic acid	HMDB
15-Hydroperoxyarachidonic acid	HMDB
Arachidonic acid 15-hydroperoxide	HMDB

Chemical Formula

C₂₀H₃₂O₄

Average Molecular Weight

336.472

Monoisotopic Molecular Weight

336.23005951

IUPAC Name

(5Z,8Z,11Z,13E)-15-hydroperoxyicosa-5,8,11,13-tetraenoic acid

Traditional Name

(5Z,8Z,11Z,13E)-15-hydroperoxyicosa-5,8,11,13-tetraenoic acid

CAS Registry Number

67675-14-3

SMILES

[H]\C(CCCC(O)=O)=C(/[H])C\C([H])=C(\[H])C\C([H])=C(\[H])C([H])=C([H])C(CCCCC)OO

InChI Identifier

InChI=1S/C20H32O4/c1-2-3-13-16-19(24-23)17-14-11-9-7-5-4-6-8-10-12-15-18-20(21)22/h4-5,8-11,14,17,19,23H,2-3,6-7,12-13,15-16,18H2,1H3,(H,21,22)/b5-4-,10-8-,11-9-,17-14+

InChI Key

BFWYTORDSFIVKP-USWFWKISSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hydroperoxyeicosatetraenoic acids. These are eicosanoic acids with an attached hydroperoxyl group and four CC double bonds.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Eicosanoids

Direct Parent

Hydroperoxyeicosatetraenoic acids

Alternative Parents

Substituents

Hydroperoxyeicosatetraenoic acid
Long-chain fatty acid
Hydroperoxy fatty acid
Fatty acid
Unsaturated fatty acid
Allylic hydroperoxide
Hydroperoxide
Carboxylic acid derivative
Alkyl hydroperoxide
Carboxylic acid
Peroxol
Monocarboxylic acid or derivatives
Carbonyl group
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Not Available

Ontology

Not Available

Exogenous (HMDB: HMDB0062688)

Process

Not Available

Role

Not Available

Physical Properties

State

Not Available

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	0.0018 g/l	ALOGPS
LogP	5.86	ALOGPS

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	5.86	ALOGPS
logP	5.81	ChemAxon
logS	-5.3	ALOGPS
pKa (Strongest Acidic)	4.82	ChemAxon
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	66.76 Å²	ChemAxon
Rotatable Bond Count	15	ChemAxon
Refractivity	102.82 m³·mol⁻¹	ChemAxon
Polarizability	39.59 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]+	191.489	31661259
DarkChem	[M-H]-	192.496	31661259
DeepCCS	[M+H]+	197.176	30932474
DeepCCS	[M-H]-	195.281	30932474
DeepCCS	[M-2H]-	228.522	30932474
DeepCCS	[M+Na]+	203.212	30932474
AllCCS	[M+H]+	190.4	32859911
AllCCS	[M+H-H2O]+	187.6	32859911
AllCCS	[M+NH4]+	193.0	32859911
AllCCS	[M+Na]+	193.8	32859911
AllCCS	[M-H]-	188.1	32859911
AllCCS	[M+Na-2H]-	190.0	32859911
AllCCS	[M+HCOO]-	192.2	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
15-HPETE	[H]\C(CCCC(O)=O)=C(/[H])C\C([H])=C(\[H])C\C([H])=C(\[H])C([H])=C([H])C(CCCCC)OO	4273.8	Standard polar	33892256
15-HPETE	[H]\C(CCCC(O)=O)=C(/[H])C\C([H])=C(\[H])C\C([H])=C(\[H])C([H])=C([H])C(CCCCC)OO	2359.4	Standard non polar	33892256
15-HPETE	[H]\C(CCCC(O)=O)=C(/[H])C\C([H])=C(\[H])C\C([H])=C(\[H])C([H])=C([H])C(CCCCC)OO	2626.0	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
15-HPETE,1TMS,isomer #1	CCCCCC(C=C/C=C\C/C=C\C/C=C\CCCC(=O)O[Si](C)(C)C)OO	2751.6	Semi standard non polar	33892256
15-HPETE,1TBDMS,isomer #1	CCCCCC(C=C/C=C\C/C=C\C/C=C\CCCC(=O)O[Si](C)(C)C(C)(C)C)OO	2993.8	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 15-HPETE GC-MS (Non-derivatized) - 70eV, Positive	splash10-00kf-8491000000-c54869ff64fb1aef9827	2017-09-20	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 15-HPETE GC-MS (1 TMS) - 70eV, Positive	splash10-00vr-9343000000-559ae101ce63837aa2c6	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 15-HPETE 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 - 15-HPETE 10V, Positive-QTOF	splash10-014i-0129000000-35e1b05b3a271d79d7fe	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 15-HPETE 20V, Positive-QTOF	splash10-066u-3494000000-2ba90c70f1436daec355	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 15-HPETE 40V, Positive-QTOF	splash10-0abc-9650000000-eacd123e3fe78937074e	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 15-HPETE 10V, Negative-QTOF	splash10-000i-0019000000-21ceecb44bdf804c0c4b	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 15-HPETE 20V, Negative-QTOF	splash10-01bi-3179000000-c6b9cc2c66aa5ec9fd58	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 15-HPETE 40V, Negative-QTOF	splash10-0a4l-9150000000-257a57d36f08ddd6cee9	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 15-HPETE 10V, Negative-QTOF	splash10-000i-0019000000-93c50c1229b4ec82a108	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 15-HPETE 20V, Negative-QTOF	splash10-0fri-1049000000-54c3cebe3c75d8538d89	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 15-HPETE 40V, Negative-QTOF	splash10-052f-9220000000-826d1d3526fa3f35755d	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 15-HPETE 10V, Positive-QTOF	splash10-0udr-1249000000-653906e8a2da4f6291b4	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 15-HPETE 20V, Positive-QTOF	splash10-100c-5596000000-9bcac41981b614f42097	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 15-HPETE 40V, Positive-QTOF	splash10-05nf-9700000000-bbdf2bdc314a07affd94	2021-09-25	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

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

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

91271

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 ]
Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.

Showing metabocard for 15-HPETE (HMDB0062688)

MOL for HMDB0062688 (15-HPETE)

3D MOL for HMDB0062688 (15-HPETE)

3D SDF for HMDB0062688 (15-HPETE)

3D-SDF for HMDB0062688 (15-HPETE)

PDB for HMDB0062688 (15-HPETE)

3D PDB for HMDB0062688 (15-HPETE)

SMILES for HMDB0062688 (15-HPETE)

INCHI for HMDB0062688 (15-HPETE)

Structure for HMDB0062688 (15-HPETE)

3D Structure for HMDB0062688 (15-HPETE)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra