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Record Information

Version

5.0

Status

Detected and Quantified

Creation Date

2013-05-01 17:29:36 UTC

Update Date

2021-09-14 14:58:08 UTC

HMDB ID

HMDB0060040

Secondary Accession Numbers

HMDB60040

Metabolite Identification

Common Name

11-HDoHE

Description

11-HDoHE belongs to the class of organic compounds known as very long-chain fatty acids. These are fatty acids with an aliphatic tail that contains at least 22 carbon atoms. 11-HDoHE is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

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

HMDB0060040
     RDKit          3D
11-HDoHE
 57 56  0  0  0  0  0  0  0  0999 V2000
  -10.4282   -0.9544   -0.5826 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2950   -0.6293   -1.5802 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2656   -1.6518   -1.5526 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0198   -1.4530   -1.2521 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5052   -0.1054   -0.8929 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4542    0.2001   -1.9012 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2015    0.4354   -1.6525 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6414    0.4289   -0.2956 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5838   -0.5913   -0.2562 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3466   -0.2810    0.0176 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9264    1.0804    0.2984 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3501    1.0861    1.7266 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0805    2.3651    2.0794 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8314    0.1701    1.7759 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0099    0.5835    1.3945 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2106   -0.2226    1.4041 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3745    0.2224    1.0155 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6315   -0.6142    1.0232 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6599   -0.0286    1.8777 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8464    0.3601    1.4937 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3187    0.2557    0.1024 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5508   -0.6319    0.1085 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0443   -0.7538   -1.2689 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4588   -0.1745   -2.2031 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.1629   -1.5131   -1.5388 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9800   -0.8855    0.4298 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.1551   -0.1141   -0.6967 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.8607   -1.9406   -0.7791 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0593    0.4002   -1.4308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8140   -0.6966   -2.5861 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5608   -2.6712   -1.8047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3141   -2.2736   -1.2555 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1881   -0.1324    0.1366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2644    0.7160   -1.0552 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7536    0.2334   -2.9711 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5285    0.6502   -2.5018 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4416    0.0764    0.4231 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3851    1.4222    0.0829 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8433   -1.6211   -0.4595 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5656   -1.0558    0.0450 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0085    1.2791   -0.3676 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5740    1.9070    0.0874 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1229    0.7836    2.4558 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5957    2.8173    2.6578 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7337   -0.8491    2.1270 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0936    1.6068    1.0449 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1959   -1.2661    1.7456 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4458    1.2468    0.6682 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3032   -1.5895    1.4894 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8937   -0.8464    0.0018 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4100    0.0966    2.9481 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5390    0.7873    2.2273 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6099    1.2868   -0.2215 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6158   -0.1872   -0.6069 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.3332   -0.2257    0.7935 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2395   -1.6237    0.5400 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.4397   -1.7308   -2.5090 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  2  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  2  0
 23 25  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  2 29  1  0
  2 30  1  0
  3 31  1  0
  4 32  1  0
  5 33  1  0
  5 34  1  0
  6 35  1  0
  7 36  1  0
  8 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
 15 46  1  0
 16 47  1  0
 17 48  1  0
 18 49  1  0
 18 50  1  0
 19 51  1  0
 20 52  1  0
 21 53  1  0
 21 54  1  0
 22 55  1  0
 22 56  1  0
 25 57  1  0
M  END


  Mrv0541 05011310292D          

 25 24  0  0  0  0            999 V2000
    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 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375   -6.4302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9500   -5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7750   -5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1875   -5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7750   -4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1875   -3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7750   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9500   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375   -2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9500   -1.4289    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7125   -2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000   -1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4750   -1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125   -0.7145    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
   -0.4125   -2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2375   -2.1434    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.8579    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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0060040

> <DATABASE_NAME>
hmdb

> <SMILES>
CC\C=C/C\C=C/C\C=C/CC(O)\C=C\C=C\C\C=C/CCC(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C22H32O3/c1-2-3-4-5-6-7-9-12-15-18-21(23)19-16-13-10-8-11-14-17-20-22(24)25/h3-4,6-7,10-16,19,21,23H,2,5,8-9,17-18,20H2,1H3,(H,24,25)/b4-3-,7-6-,13-10+,14-11-,15-12-,19-16+

> <INCHI_KEY>
LTERDCBCHFKFRI-KEFMQFBKSA-N

> <FORMULA>
C22H32O3

> <MOLECULAR_WEIGHT>
344.4877

> <EXACT_MASS>
344.23514489

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_AVERAGE_POLARIZABILITY>
40.33228722459342

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(4Z,7E,9E,13Z,16Z,19Z)-11-hydroxydocosa-4,7,9,13,16,19-hexaenoic acid

> <ALOGPS_LOGP>
5.95

> <JCHEM_LOGP>
5.521653760666666

> <ALOGPS_LOGS>
-5.44

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
17.72081992917354

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.8528649941627195

> <JCHEM_PKA_STRONGEST_BASIC>
-1.6087135130191386

> <JCHEM_POLAR_SURFACE_AREA>
57.53

> <JCHEM_REFRACTIVITY>
112.9047

> <JCHEM_ROTATABLE_BOND_COUNT>
14

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.24e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(4Z,7E,9E,13Z,16Z,19Z)-11-hydroxydocosa-4,7,9,13,16,19-hexaenoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0060040
     RDKit          3D
11-HDoHE
 57 56  0  0  0  0  0  0  0  0999 V2000
  -10.4282   -0.9544   -0.5826 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2950   -0.6293   -1.5802 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2656   -1.6518   -1.5526 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0198   -1.4530   -1.2521 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5052   -0.1054   -0.8929 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4542    0.2001   -1.9012 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2015    0.4354   -1.6525 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6414    0.4289   -0.2956 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5838   -0.5913   -0.2562 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3466   -0.2810    0.0176 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9264    1.0804    0.2984 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3501    1.0861    1.7266 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0805    2.3651    2.0794 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8314    0.1701    1.7759 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0099    0.5835    1.3945 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2106   -0.2226    1.4041 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3745    0.2224    1.0155 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6315   -0.6142    1.0232 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6599   -0.0286    1.8777 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8464    0.3601    1.4937 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3187    0.2557    0.1024 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5508   -0.6319    0.1085 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0443   -0.7538   -1.2689 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4588   -0.1745   -2.2031 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.1629   -1.5131   -1.5388 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9800   -0.8855    0.4298 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.1551   -0.1141   -0.6967 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.8607   -1.9406   -0.7791 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0593    0.4002   -1.4308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8140   -0.6966   -2.5861 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5608   -2.6712   -1.8047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3141   -2.2736   -1.2555 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1881   -0.1324    0.1366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2644    0.7160   -1.0552 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7536    0.2334   -2.9711 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5285    0.6502   -2.5018 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4416    0.0764    0.4231 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3851    1.4222    0.0829 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8433   -1.6211   -0.4595 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5656   -1.0558    0.0450 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0085    1.2791   -0.3676 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5740    1.9070    0.0874 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1229    0.7836    2.4558 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5957    2.8173    2.6578 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7337   -0.8491    2.1270 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0936    1.6068    1.0449 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1959   -1.2661    1.7456 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4458    1.2468    0.6682 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3032   -1.5895    1.4894 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8937   -0.8464    0.0018 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4100    0.0966    2.9481 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5390    0.7873    2.2273 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6099    1.2868   -0.2215 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6158   -0.1872   -0.6069 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.3332   -0.2257    0.7935 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2395   -1.6237    0.5400 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.4397   -1.7308   -2.5090 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  2  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  2  0
 23 25  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  2 29  1  0
  2 30  1  0
  3 31  1  0
  4 32  1  0
  5 33  1  0
  5 34  1  0
  6 35  1  0
  7 36  1  0
  8 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
 15 46  1  0
 16 47  1  0
 17 48  1  0
 18 49  1  0
 18 50  1  0
 19 51  1  0
 20 52  1  0
 21 53  1  0
 21 54  1  0
 22 55  1  0
 22 56  1  0
 25 57  1  0
M  END

HEADER    PROTEIN                                 01-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   01-MAY-13         0                                  
HETATM    1  C   UNK     0       4.620 -10.669   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.160 -10.669   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.930 -12.003   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.470 -12.003   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.240 -10.669   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.780 -10.669   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      11.550  -9.336   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      10.780  -8.002   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      11.550  -6.668   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.780  -5.335   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.240  -5.335   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.470  -4.001   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       9.240  -2.667   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       6.930  -4.001   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.160  -2.667   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.620  -2.667   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.850  -1.334   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.310  -1.334   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.540   0.000   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -0.770  -1.334   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.000  -2.667   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -0.770  -4.001   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -2.310  -4.001   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       0.000  -5.335   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   48    0
END

COMPND    HMDB0060040
HETATM    1  C1  UNL     1     -10.428  -0.954  -0.583  1.00  0.00           C  
HETATM    2  C2  UNL     1      -9.295  -0.629  -1.580  1.00  0.00           C  
HETATM    3  C3  UNL     1      -8.266  -1.652  -1.553  1.00  0.00           C  
HETATM    4  C4  UNL     1      -7.020  -1.453  -1.252  1.00  0.00           C  
HETATM    5  C5  UNL     1      -6.505  -0.105  -0.893  1.00  0.00           C  
HETATM    6  C6  UNL     1      -5.454   0.200  -1.901  1.00  0.00           C  
HETATM    7  C7  UNL     1      -4.202   0.435  -1.652  1.00  0.00           C  
HETATM    8  C8  UNL     1      -3.641   0.429  -0.296  1.00  0.00           C  
HETATM    9  C9  UNL     1      -2.584  -0.591  -0.256  1.00  0.00           C  
HETATM   10  C10 UNL     1      -1.347  -0.281   0.018  1.00  0.00           C  
HETATM   11  C11 UNL     1      -0.926   1.080   0.298  1.00  0.00           C  
HETATM   12  C12 UNL     1      -0.350   1.086   1.727  1.00  0.00           C  
HETATM   13  O1  UNL     1       0.080   2.365   2.079  1.00  0.00           O  
HETATM   14  C13 UNL     1       0.831   0.170   1.776  1.00  0.00           C  
HETATM   15  C14 UNL     1       2.010   0.583   1.394  1.00  0.00           C  
HETATM   16  C15 UNL     1       3.211  -0.223   1.404  1.00  0.00           C  
HETATM   17  C16 UNL     1       4.374   0.222   1.016  1.00  0.00           C  
HETATM   18  C17 UNL     1       5.632  -0.614   1.023  1.00  0.00           C  
HETATM   19  C18 UNL     1       6.660  -0.029   1.878  1.00  0.00           C  
HETATM   20  C19 UNL     1       7.846   0.360   1.494  1.00  0.00           C  
HETATM   21  C20 UNL     1       8.319   0.256   0.102  1.00  0.00           C  
HETATM   22  C21 UNL     1       9.551  -0.632   0.109  1.00  0.00           C  
HETATM   23  C22 UNL     1      10.044  -0.754  -1.269  1.00  0.00           C  
HETATM   24  O2  UNL     1       9.459  -0.174  -2.203  1.00  0.00           O  
HETATM   25  O3  UNL     1      11.163  -1.513  -1.539  1.00  0.00           O  
HETATM   26  H1  UNL     1      -9.980  -0.886   0.430  1.00  0.00           H  
HETATM   27  H2  UNL     1     -11.155  -0.114  -0.697  1.00  0.00           H  
HETATM   28  H3  UNL     1     -10.861  -1.941  -0.779  1.00  0.00           H  
HETATM   29  H4  UNL     1      -9.059   0.400  -1.431  1.00  0.00           H  
HETATM   30  H5  UNL     1      -9.814  -0.697  -2.586  1.00  0.00           H  
HETATM   31  H6  UNL     1      -8.561  -2.671  -1.805  1.00  0.00           H  
HETATM   32  H7  UNL     1      -6.314  -2.274  -1.256  1.00  0.00           H  
HETATM   33  H8  UNL     1      -6.188  -0.132   0.137  1.00  0.00           H  
HETATM   34  H9  UNL     1      -7.264   0.716  -1.055  1.00  0.00           H  
HETATM   35  H10 UNL     1      -5.754   0.233  -2.971  1.00  0.00           H  
HETATM   36  H11 UNL     1      -3.529   0.650  -2.502  1.00  0.00           H  
HETATM   37  H12 UNL     1      -4.442   0.076   0.423  1.00  0.00           H  
HETATM   38  H13 UNL     1      -3.385   1.422   0.083  1.00  0.00           H  
HETATM   39  H14 UNL     1      -2.843  -1.621  -0.459  1.00  0.00           H  
HETATM   40  H15 UNL     1      -0.566  -1.056   0.045  1.00  0.00           H  
HETATM   41  H16 UNL     1      -0.008   1.279  -0.368  1.00  0.00           H  
HETATM   42  H17 UNL     1      -1.574   1.907   0.087  1.00  0.00           H  
HETATM   43  H18 UNL     1      -1.123   0.784   2.456  1.00  0.00           H  
HETATM   44  H19 UNL     1      -0.596   2.817   2.658  1.00  0.00           H  
HETATM   45  H20 UNL     1       0.734  -0.849   2.127  1.00  0.00           H  
HETATM   46  H21 UNL     1       2.094   1.607   1.045  1.00  0.00           H  
HETATM   47  H22 UNL     1       3.196  -1.266   1.746  1.00  0.00           H  
HETATM   48  H23 UNL     1       4.446   1.247   0.668  1.00  0.00           H  
HETATM   49  H24 UNL     1       5.303  -1.590   1.489  1.00  0.00           H  
HETATM   50  H25 UNL     1       5.894  -0.846   0.002  1.00  0.00           H  
HETATM   51  H26 UNL     1       6.410   0.097   2.948  1.00  0.00           H  
HETATM   52  H27 UNL     1       8.539   0.787   2.227  1.00  0.00           H  
HETATM   53  H28 UNL     1       8.610   1.287  -0.221  1.00  0.00           H  
HETATM   54  H29 UNL     1       7.616  -0.187  -0.607  1.00  0.00           H  
HETATM   55  H30 UNL     1      10.333  -0.226   0.793  1.00  0.00           H  
HETATM   56  H31 UNL     1       9.240  -1.624   0.540  1.00  0.00           H  
HETATM   57  H32 UNL     1      11.440  -1.731  -2.509  1.00  0.00           H  
CONECT    1    2   26   27   28
CONECT    2    3   29   30
CONECT    3    4    4   31
CONECT    4    5   32
CONECT    5    6   33   34
CONECT    6    7    7   35
CONECT    7    8   36
CONECT    8    9   37   38
CONECT    9   10   10   39
CONECT   10   11   40
CONECT   11   12   41   42
CONECT   12   13   14   43
CONECT   13   44
CONECT   14   15   15   45
CONECT   15   16   46
CONECT   16   17   17   47
CONECT   17   18   48
CONECT   18   19   49   50
CONECT   19   20   20   51
CONECT   20   21   52
CONECT   21   22   53   54
CONECT   22   23   55   56
CONECT   23   24   24   25
CONECT   25   57
END

HMDB0060040
     RDKit          3D
11-HDoHE
 57 56  0  0  0  0  0  0  0  0999 V2000
  -10.4282   -0.9544   -0.5826 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2950   -0.6293   -1.5802 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2656   -1.6518   -1.5526 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0198   -1.4530   -1.2521 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5052   -0.1054   -0.8929 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4542    0.2001   -1.9012 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2015    0.4354   -1.6525 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6414    0.4289   -0.2956 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5838   -0.5913   -0.2562 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3466   -0.2810    0.0176 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9264    1.0804    0.2984 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3501    1.0861    1.7266 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0805    2.3651    2.0794 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8314    0.1701    1.7759 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0099    0.5835    1.3945 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2106   -0.2226    1.4041 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3745    0.2224    1.0155 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6315   -0.6142    1.0232 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6599   -0.0286    1.8777 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8464    0.3601    1.4937 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3187    0.2557    0.1024 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5508   -0.6319    0.1085 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0443   -0.7538   -1.2689 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4588   -0.1745   -2.2031 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.1629   -1.5131   -1.5388 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9800   -0.8855    0.4298 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.1551   -0.1141   -0.6967 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.8607   -1.9406   -0.7791 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0593    0.4002   -1.4308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8140   -0.6966   -2.5861 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5608   -2.6712   -1.8047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3141   -2.2736   -1.2555 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1881   -0.1324    0.1366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2644    0.7160   -1.0552 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7536    0.2334   -2.9711 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5285    0.6502   -2.5018 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4416    0.0764    0.4231 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3851    1.4222    0.0829 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8433   -1.6211   -0.4595 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5656   -1.0558    0.0450 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0085    1.2791   -0.3676 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5740    1.9070    0.0874 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1229    0.7836    2.4558 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5957    2.8173    2.6578 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7337   -0.8491    2.1270 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0936    1.6068    1.0449 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1959   -1.2661    1.7456 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4458    1.2468    0.6682 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3032   -1.5895    1.4894 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8937   -0.8464    0.0018 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4100    0.0966    2.9481 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5390    0.7873    2.2273 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6099    1.2868   -0.2215 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6158   -0.1872   -0.6069 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.3332   -0.2257    0.7935 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2395   -1.6237    0.5400 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.4397   -1.7308   -2.5090 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  2  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  2  0
 23 25  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  2 29  1  0
  2 30  1  0
  3 31  1  0
  4 32  1  0
  5 33  1  0
  5 34  1  0
  6 35  1  0
  7 36  1  0
  8 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
 15 46  1  0
 16 47  1  0
 17 48  1  0
 18 49  1  0
 18 50  1  0
 19 51  1  0
 20 52  1  0
 21 53  1  0
 21 54  1  0
 22 55  1  0
 22 56  1  0
 25 57  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
(4Z,7E,9E,13Z,16Z,19Z)-11-Hydroxydocosa-4,7,9,13,16,19-hexaenoate	Generator

Chemical Formula

C₂₂H₃₂O₃

Average Molecular Weight

344.4877

Monoisotopic Molecular Weight

344.23514489

IUPAC Name

(4Z,7E,9E,13Z,16Z,19Z)-11-hydroxydocosa-4,7,9,13,16,19-hexaenoic acid

Traditional Name

(4Z,7E,9E,13Z,16Z,19Z)-11-hydroxydocosa-4,7,9,13,16,19-hexaenoic acid

CAS Registry Number

Not Available

SMILES

CC\C=C/C\C=C/C\C=C/CC(O)\C=C\C=C\C\C=C/CCC(O)=O

InChI Identifier

InChI=1S/C22H32O3/c1-2-3-4-5-6-7-9-12-15-18-21(23)19-16-13-10-8-11-14-17-20-22(24)25/h3-4,6-7,10-16,19,21,23H,2,5,8-9,17-18,20H2,1H3,(H,24,25)/b4-3-,7-6-,13-10+,14-11-,15-12-,19-16+

InChI Key

LTERDCBCHFKFRI-KEFMQFBKSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as very long-chain fatty acids. These are fatty acids with an aliphatic tail that contains at least 22 carbon atoms.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acids and conjugates

Direct Parent

Very long-chain fatty acids

Alternative Parents

Substituents

Very long-chain fatty acid
Hydroxy fatty acid
Unsaturated fatty acid
Secondary alcohol
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 20671299)

Cellular substructure

Membrane (HMDB: HMDB0060040)

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	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.0012 g/L	ALOGPS
logP	5.95	ALOGPS
logP	5.52	ChemAxon
logS	-5.4	ALOGPS
pKa (Strongest Acidic)	4.85	ChemAxon
pKa (Strongest Basic)	-1.6	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	57.53 Å²	ChemAxon
Rotatable Bond Count	14	ChemAxon
Refractivity	112.9 m³·mol⁻¹	ChemAxon
Polarizability	40.33 Å³	ChemAxon
Number of Rings	0	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]+	193.972	31661259
DarkChem	[M-H]-	194.224	31661259
DeepCCS	[M+H]+	188.566	30932474
DeepCCS	[M-H]-	186.208	30932474
DeepCCS	[M-2H]-	219.443	30932474
DeepCCS	[M+Na]+	194.67	30932474
AllCCS	[M+H]+	193.0	32859911
AllCCS	[M+H-H2O]+	190.2	32859911
AllCCS	[M+NH4]+	195.6	32859911
AllCCS	[M+Na]+	196.4	32859911
AllCCS	[M-H]-	188.8	32859911
AllCCS	[M+Na-2H]-	190.7	32859911
AllCCS	[M+HCOO]-	193.0	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
11-HDoHE	CC\C=C/C\C=C/C\C=C/CC(O)\C=C\C=C\C\C=C/CCC(O)=O	4594.3	Standard polar	33892256
11-HDoHE	CC\C=C/C\C=C/C\C=C/CC(O)\C=C\C=C\C\C=C/CCC(O)=O	2548.3	Standard non polar	33892256
11-HDoHE	CC\C=C/C\C=C/C\C=C/CC(O)\C=C\C=C\C\C=C/CCC(O)=O	2760.9	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
11-HDoHE,1TMS,isomer #1	CC/C=C\C/C=C\C/C=C\CC(/C=C/C=C/C/C=C\CCC(=O)O)O[Si](C)(C)C	3013.3	Semi standard non polar	33892256
11-HDoHE,1TMS,isomer #2	CC/C=C\C/C=C\C/C=C\CC(O)/C=C/C=C/C/C=C\CCC(=O)O[Si](C)(C)C	2858.3	Semi standard non polar	33892256
11-HDoHE,2TMS,isomer #1	CC/C=C\C/C=C\C/C=C\CC(/C=C/C=C/C/C=C\CCC(=O)O[Si](C)(C)C)O[Si](C)(C)C	2899.9	Semi standard non polar	33892256
11-HDoHE,1TBDMS,isomer #1	CC/C=C\C/C=C\C/C=C\CC(/C=C/C=C/C/C=C\CCC(=O)O)O[Si](C)(C)C(C)(C)C	3245.2	Semi standard non polar	33892256
11-HDoHE,1TBDMS,isomer #2	CC/C=C\C/C=C\C/C=C\CC(O)/C=C/C=C/C/C=C\CCC(=O)O[Si](C)(C)C(C)(C)C	3098.3	Semi standard non polar	33892256
11-HDoHE,2TBDMS,isomer #1	CC/C=C\C/C=C\C/C=C\CC(/C=C/C=C/C/C=C\CCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3373.3	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 - 11-HDoHE GC-MS (Non-derivatized) - 70eV, Positive	splash10-002b-2933000000-5f0a7376effcf539800a	2017-09-20	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 11-HDoHE GC-MS (2 TMS) - 70eV, Positive	splash10-00fs-9214400000-6459c90ff112f0e9aebb	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 11-HDoHE 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-HDoHE 10V, Positive-QTOF	splash10-004i-0019000000-0ec3ba5dea581d21e544	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 11-HDoHE 20V, Positive-QTOF	splash10-00nb-3965000000-18cfeef693f7c278dcfa	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 11-HDoHE 40V, Positive-QTOF	splash10-0673-6940000000-68642bdad9289923e84b	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 11-HDoHE 10V, Negative-QTOF	splash10-0006-0019000000-b1b896d5f16dfad71b48	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 11-HDoHE 20V, Negative-QTOF	splash10-004m-1239000000-c39d0885d546cee5d898	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 11-HDoHE 40V, Negative-QTOF	splash10-0a4l-9820000000-aceb8ecb8ed50de739fa	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 11-HDoHE 10V, Positive-QTOF	splash10-004i-0019000000-c953f8d61ae1eb986c2c	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 11-HDoHE 20V, Positive-QTOF	splash10-057l-8398000000-a59d050acac758def8a5	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 11-HDoHE 40V, Positive-QTOF	splash10-00l6-9320000000-e347451900f01ec53aac	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 11-HDoHE 10V, Negative-QTOF	splash10-0006-0009000000-831bd066b29ec5e6aa8b	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 11-HDoHE 20V, Negative-QTOF	splash10-002f-0309000000-d753593df6e2324f59a4	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 11-HDoHE 40V, Negative-QTOF	splash10-0ab9-2590000000-cae10e80466826192306	2021-10-12	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	0.000175 +/- 0.000005 uM	Adult (>18 years old)	Both	Normal	20671299	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

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

131769802

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

Quehenberger O, Armando AM, Brown AH, Milne SB, Myers DS, Merrill AH, Bandyopadhyay S, Jones KN, Kelly S, Shaner RL, Sullards CM, Wang E, Murphy RC, Barkley RM, Leiker TJ, Raetz CR, Guan Z, Laird GM, Six DA, Russell DW, McDonald JG, Subramaniam S, Fahy E, Dennis EA: Lipidomics reveals a remarkable diversity of lipids in human plasma. J Lipid Res. 2010 Nov;51(11):3299-305. doi: 10.1194/jlr.M009449. Epub 2010 Jul 29. [PubMed:20671299 ]
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 11-HDoHE (HMDB0060040)

MOL for HMDB0060040 (11-HDoHE)

3D MOL for HMDB0060040 (11-HDoHE)

3D SDF for HMDB0060040 (11-HDoHE)

3D-SDF for HMDB0060040 (11-HDoHE)

PDB for HMDB0060040 (11-HDoHE)

3D PDB for HMDB0060040 (11-HDoHE)

SMILES for HMDB0060040 (11-HDoHE)

INCHI for HMDB0060040 (11-HDoHE)

Structure for HMDB0060040 (11-HDoHE)

3D Structure for HMDB0060040 (11-HDoHE)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra