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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2013-05-09 20:54:37 UTC

Update Date

2022-03-07 03:17:39 UTC

HMDB ID

HMDB0060101

Secondary Accession Numbers

HMDB60101

Metabolite Identification

Common Name

12 Hydroxy arachidonic acid

Description

12 Hydroxy arachidonic acid belongs to the class of organic compounds known as long-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 13 and 21 carbon atoms. 12 Hydroxy arachidonic acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

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

HMDB0060101
     RDKit          3D
12 Hydroxy arachidonic acid
 55 54  0  0  0  0  0  0  0  0999 V2000
   -7.6749   -1.2066   -0.9192 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0961   -0.9703    0.4559 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6463    0.4561    0.5300 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6110    0.7542   -0.5189 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4200   -0.1551   -0.2835 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3411    0.0634   -1.2397 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1432    0.4426   -0.9002 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7561    0.6936    0.4985 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3069    2.1096    0.5648 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2553    3.0734    0.2206 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0951    2.3623    0.9278 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9616    1.4262    1.3040 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0801    1.6308    0.3493 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5881    0.7483   -0.4781 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0637   -0.6275   -0.5497 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1507   -1.5918   -0.1993 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3683   -1.1719    0.1163 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4545   -2.1407    0.4665 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6154   -2.0291   -0.4659 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2790   -0.6969   -0.5050 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8415   -0.2584    0.7919 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7581   -0.9766    1.8064 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4682    0.9737    0.8633 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9652   -1.8721   -1.4594 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8471   -0.2677   -1.4820 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6382   -1.7818   -0.8376 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2815   -1.6443    0.7269 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9341   -1.1042    1.1904 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2207    0.7092    1.5393 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5378    1.1414    0.4330 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3420    1.8246   -0.4220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0089    0.6141   -1.5401 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8422   -1.1933   -0.5720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1994   -0.2585    0.7601 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5367   -0.1000   -2.3267 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3374    0.6010   -1.6438 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6422    0.6781    1.2011 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0773   -0.0414    0.9151 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1095    4.0562    0.4029 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1852    3.4298    0.9587 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7350    0.3915    1.4174 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3733    1.8550    2.3005 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5659    2.6337    0.3034 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4359    1.0559   -1.1414 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7891   -0.7746   -1.6465 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1833   -0.8113    0.0401 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9566   -2.6525   -0.1987 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5418   -0.0979    0.1103 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7493   -2.0938    1.5161 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0308   -3.1701    0.3162 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3731   -2.7816   -0.1445 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3068   -2.2808   -1.5004 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6026    0.1075   -0.8630 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0916   -0.7635   -1.2775 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3169    1.6823    0.1568 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
  9 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
  1 24  1  0
  1 25  1  0
  1 26  1  0
  2 27  1  0
  2 28  1  0
  3 29  1  0
  3 30  1  0
  4 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
 10 39  1  0
 11 40  1  0
 12 41  1  0
 12 42  1  0
 13 43  1  0
 14 44  1  0
 15 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
 19 52  1  0
 20 53  1  0
 20 54  1  0
 23 55  1  0
M  END


  Mrv0541 08071417402D          

 23 22  0  0  0  0            999 V2000
   -7.3362    2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6217    1.9520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9071    2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1927    1.9520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4783    2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6204    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9059    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3349    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1913    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7638    1.9520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3349    1.9520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5230    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0492    2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6204    2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2374    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0492    3.1894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6204    3.1894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3349    3.6020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6664    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3349    4.4269    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3809    1.1270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6664   -0.1105    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0  0  0  0
  3  2  1  0  0  0  0
  4  3  1  0  0  0  0
  5  4  1  0  0  0  0
  7  6  1  0  0  0  0
  8  6  1  0  0  0  0
  9  7  2  0  0  0  0
 10  5  1  0  0  0  0
 11  8  2  0  0  0  0
 12  9  1  0  0  0  0
 13 10  2  0  0  0  0
 14 11  1  0  0  0  0
 15 12  1  0  0  0  0
 16 13  1  0  0  0  0
 17 14  1  0  0  0  0
 18 15  1  0  0  0  0
 19 16  1  0  0  0  0
 19 17  2  0  0  0  0
 20 18  1  0  0  0  0
 21 19  1  0  0  0  0
 22 20  2  0  0  0  0
 23 20  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0060101

> <DATABASE_NAME>
hmdb

> <SMILES>
CCCCC\C=C/C\C(O)=C/C\C=C/C\C=C\CCCC(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C20H32O3/c1-2-3-4-5-10-13-16-19(21)17-14-11-8-6-7-9-12-15-18-20(22)23/h7-11,13,17,21H,2-6,12,14-16,18H2,1H3,(H,22,23)/b9-7+,11-8-,13-10-,19-17+

> <INCHI_KEY>
HVRRTPWRYUQZPF-RMOYYRCGSA-N

> <FORMULA>
C20H32O3

> <MOLECULAR_WEIGHT>
320.4663

> <EXACT_MASS>
320.23514489

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
38.1008011748518

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(5E,8Z,11E,14Z)-12-hydroxyicosa-5,8,11,14-tetraenoic acid

> <ALOGPS_LOGP>
6.00

> <JCHEM_LOGP>
5.760416451999999

> <ALOGPS_LOGS>
-5.31

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
10.41867839203897

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.819770746872386

> <JCHEM_PKA_STRONGEST_BASIC>
-4.802670549684607

> <JCHEM_POLAR_SURFACE_AREA>
57.53

> <JCHEM_REFRACTIVITY>
102.00029999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
14

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.58e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(5E,8Z,11E,14Z)-12-hydroxyicosa-5,8,11,14-tetraenoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0060101
     RDKit          3D
12 Hydroxy arachidonic acid
 55 54  0  0  0  0  0  0  0  0999 V2000
   -7.6749   -1.2066   -0.9192 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0961   -0.9703    0.4559 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6463    0.4561    0.5300 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6110    0.7542   -0.5189 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4200   -0.1551   -0.2835 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3411    0.0634   -1.2397 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1432    0.4426   -0.9002 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7561    0.6936    0.4985 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3069    2.1096    0.5648 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2553    3.0734    0.2206 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0951    2.3623    0.9278 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9616    1.4262    1.3040 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0801    1.6308    0.3493 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5881    0.7483   -0.4781 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0637   -0.6275   -0.5497 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1507   -1.5918   -0.1993 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3683   -1.1719    0.1163 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4545   -2.1407    0.4665 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6154   -2.0291   -0.4659 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2790   -0.6969   -0.5050 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8415   -0.2584    0.7919 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7581   -0.9766    1.8064 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4682    0.9737    0.8633 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9652   -1.8721   -1.4594 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8471   -0.2677   -1.4820 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6382   -1.7818   -0.8376 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2815   -1.6443    0.7269 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9341   -1.1042    1.1904 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2207    0.7092    1.5393 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5378    1.1414    0.4330 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3420    1.8246   -0.4220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0089    0.6141   -1.5401 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8422   -1.1933   -0.5720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1994   -0.2585    0.7601 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5367   -0.1000   -2.3267 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3374    0.6010   -1.6438 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6422    0.6781    1.2011 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0773   -0.0414    0.9151 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1095    4.0562    0.4029 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1852    3.4298    0.9587 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7350    0.3915    1.4174 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3733    1.8550    2.3005 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5659    2.6337    0.3034 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4359    1.0559   -1.1414 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7891   -0.7746   -1.6465 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1833   -0.8113    0.0401 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9566   -2.6525   -0.1987 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5418   -0.0979    0.1103 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7493   -2.0938    1.5161 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0308   -3.1701    0.3162 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3731   -2.7816   -0.1445 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3068   -2.2808   -1.5004 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6026    0.1075   -0.8630 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0916   -0.7635   -1.2775 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3169    1.6823    0.1568 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
  9 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
  1 24  1  0
  1 25  1  0
  1 26  1  0
  2 27  1  0
  2 28  1  0
  3 29  1  0
  3 30  1  0
  4 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
 10 39  1  0
 11 40  1  0
 12 41  1  0
 12 42  1  0
 13 43  1  0
 14 44  1  0
 15 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
 19 52  1  0
 20 53  1  0
 20 54  1  0
 23 55  1  0
M  END

HEADER    PROTEIN                                 07-AUG-14   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-AUG-14         0                                  
HETATM    1  C   UNK     0     -13.694   4.414   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -12.361   3.644   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -11.027   4.414   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -9.693   3.644   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -8.359   4.414   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -3.025   1.334   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.691   2.104   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -4.358   2.104   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.357   1.334   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -7.026   3.644   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -4.358   3.644   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.976   2.104   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -5.692   4.414   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -3.025   4.414   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.310   1.334   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -5.692   5.954   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -3.025   5.954   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.644   2.104   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -4.358   6.724   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.977   1.334   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -4.358   8.264   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       6.311   2.104   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       4.977  -0.206   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   10                                                       
CONECT    6    7    8                                                       
CONECT    7    6    9                                                       
CONECT    8    6   11                                                       
CONECT    9    7   12                                                       
CONECT   10    5   13                                                       
CONECT   11    8   14                                                       
CONECT   12    9   15                                                       
CONECT   13   10   16                                                       
CONECT   14   11   17                                                       
CONECT   15   12   18                                                       
CONECT   16   13   19                                                       
CONECT   17   14   19                                                       
CONECT   18   15   20                                                       
CONECT   19   16   17   21                                                  
CONECT   20   18   22   23                                                  
CONECT   21   19                                                            
CONECT   22   20                                                            
CONECT   23   20                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   44    0
END

COMPND    HMDB0060101
HETATM    1  C1  UNL     1      -7.675  -1.207  -0.919  1.00  0.00           C  
HETATM    2  C2  UNL     1      -7.096  -0.970   0.456  1.00  0.00           C  
HETATM    3  C3  UNL     1      -6.646   0.456   0.530  1.00  0.00           C  
HETATM    4  C4  UNL     1      -5.611   0.754  -0.519  1.00  0.00           C  
HETATM    5  C5  UNL     1      -4.420  -0.155  -0.284  1.00  0.00           C  
HETATM    6  C6  UNL     1      -3.341   0.063  -1.240  1.00  0.00           C  
HETATM    7  C7  UNL     1      -2.143   0.443  -0.900  1.00  0.00           C  
HETATM    8  C8  UNL     1      -1.756   0.694   0.499  1.00  0.00           C  
HETATM    9  C9  UNL     1      -1.307   2.110   0.565  1.00  0.00           C  
HETATM   10  O1  UNL     1      -2.255   3.073   0.221  1.00  0.00           O  
HETATM   11  C10 UNL     1      -0.095   2.362   0.928  1.00  0.00           C  
HETATM   12  C11 UNL     1       0.962   1.426   1.304  1.00  0.00           C  
HETATM   13  C12 UNL     1       2.080   1.631   0.349  1.00  0.00           C  
HETATM   14  C13 UNL     1       2.588   0.748  -0.478  1.00  0.00           C  
HETATM   15  C14 UNL     1       2.064  -0.628  -0.550  1.00  0.00           C  
HETATM   16  C15 UNL     1       3.151  -1.592  -0.199  1.00  0.00           C  
HETATM   17  C16 UNL     1       4.368  -1.172   0.116  1.00  0.00           C  
HETATM   18  C17 UNL     1       5.454  -2.141   0.466  1.00  0.00           C  
HETATM   19  C18 UNL     1       6.615  -2.029  -0.466  1.00  0.00           C  
HETATM   20  C19 UNL     1       7.279  -0.697  -0.505  1.00  0.00           C  
HETATM   21  C20 UNL     1       7.841  -0.258   0.792  1.00  0.00           C  
HETATM   22  O2  UNL     1       7.758  -0.977   1.806  1.00  0.00           O  
HETATM   23  O3  UNL     1       8.468   0.974   0.863  1.00  0.00           O  
HETATM   24  H1  UNL     1      -6.965  -1.872  -1.459  1.00  0.00           H  
HETATM   25  H2  UNL     1      -7.847  -0.268  -1.482  1.00  0.00           H  
HETATM   26  H3  UNL     1      -8.638  -1.782  -0.838  1.00  0.00           H  
HETATM   27  H4  UNL     1      -6.282  -1.644   0.727  1.00  0.00           H  
HETATM   28  H5  UNL     1      -7.934  -1.104   1.190  1.00  0.00           H  
HETATM   29  H6  UNL     1      -6.221   0.709   1.539  1.00  0.00           H  
HETATM   30  H7  UNL     1      -7.538   1.141   0.433  1.00  0.00           H  
HETATM   31  H8  UNL     1      -5.342   1.825  -0.422  1.00  0.00           H  
HETATM   32  H9  UNL     1      -6.009   0.614  -1.540  1.00  0.00           H  
HETATM   33  H10 UNL     1      -4.842  -1.193  -0.572  1.00  0.00           H  
HETATM   34  H11 UNL     1      -4.199  -0.259   0.760  1.00  0.00           H  
HETATM   35  H12 UNL     1      -3.537  -0.100  -2.327  1.00  0.00           H  
HETATM   36  H13 UNL     1      -1.337   0.601  -1.644  1.00  0.00           H  
HETATM   37  H14 UNL     1      -2.642   0.678   1.201  1.00  0.00           H  
HETATM   38  H15 UNL     1      -1.077  -0.041   0.915  1.00  0.00           H  
HETATM   39  H16 UNL     1      -2.109   4.056   0.403  1.00  0.00           H  
HETATM   40  H17 UNL     1       0.185   3.430   0.959  1.00  0.00           H  
HETATM   41  H18 UNL     1       0.735   0.392   1.417  1.00  0.00           H  
HETATM   42  H19 UNL     1       1.373   1.855   2.301  1.00  0.00           H  
HETATM   43  H20 UNL     1       2.566   2.634   0.303  1.00  0.00           H  
HETATM   44  H21 UNL     1       3.436   1.056  -1.141  1.00  0.00           H  
HETATM   45  H22 UNL     1       1.789  -0.775  -1.647  1.00  0.00           H  
HETATM   46  H23 UNL     1       1.183  -0.811   0.040  1.00  0.00           H  
HETATM   47  H24 UNL     1       2.957  -2.652  -0.199  1.00  0.00           H  
HETATM   48  H25 UNL     1       4.542  -0.098   0.110  1.00  0.00           H  
HETATM   49  H26 UNL     1       5.749  -2.094   1.516  1.00  0.00           H  
HETATM   50  H27 UNL     1       5.031  -3.170   0.316  1.00  0.00           H  
HETATM   51  H28 UNL     1       7.373  -2.782  -0.145  1.00  0.00           H  
HETATM   52  H29 UNL     1       6.307  -2.281  -1.500  1.00  0.00           H  
HETATM   53  H30 UNL     1       6.603   0.107  -0.863  1.00  0.00           H  
HETATM   54  H31 UNL     1       8.092  -0.764  -1.277  1.00  0.00           H  
HETATM   55  H32 UNL     1       8.317   1.682   0.157  1.00  0.00           H  
CONECT    1    2   24   25   26
CONECT    2    3   27   28
CONECT    3    4   29   30
CONECT    4    5   31   32
CONECT    5    6   33   34
CONECT    6    7    7   35
CONECT    7    8   36
CONECT    8    9   37   38
CONECT    9   10   11   11
CONECT   10   39
CONECT   11   12   40
CONECT   12   13   41   42
CONECT   13   14   14   43
CONECT   14   15   44
CONECT   15   16   45   46
CONECT   16   17   17   47
CONECT   17   18   48
CONECT   18   19   49   50
CONECT   19   20   51   52
CONECT   20   21   53   54
CONECT   21   22   22   23
CONECT   23   55
END

HMDB0060101
     RDKit          3D
12 Hydroxy arachidonic acid
 55 54  0  0  0  0  0  0  0  0999 V2000
   -7.6749   -1.2066   -0.9192 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0961   -0.9703    0.4559 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6463    0.4561    0.5300 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6110    0.7542   -0.5189 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4200   -0.1551   -0.2835 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3411    0.0634   -1.2397 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1432    0.4426   -0.9002 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7561    0.6936    0.4985 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3069    2.1096    0.5648 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2553    3.0734    0.2206 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0951    2.3623    0.9278 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9616    1.4262    1.3040 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0801    1.6308    0.3493 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5881    0.7483   -0.4781 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0637   -0.6275   -0.5497 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1507   -1.5918   -0.1993 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3683   -1.1719    0.1163 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4545   -2.1407    0.4665 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6154   -2.0291   -0.4659 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2790   -0.6969   -0.5050 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8415   -0.2584    0.7919 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7581   -0.9766    1.8064 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4682    0.9737    0.8633 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9652   -1.8721   -1.4594 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8471   -0.2677   -1.4820 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6382   -1.7818   -0.8376 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2815   -1.6443    0.7269 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9341   -1.1042    1.1904 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2207    0.7092    1.5393 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5378    1.1414    0.4330 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3420    1.8246   -0.4220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0089    0.6141   -1.5401 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8422   -1.1933   -0.5720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1994   -0.2585    0.7601 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5367   -0.1000   -2.3267 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3374    0.6010   -1.6438 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6422    0.6781    1.2011 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0773   -0.0414    0.9151 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1095    4.0562    0.4029 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1852    3.4298    0.9587 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7350    0.3915    1.4174 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3733    1.8550    2.3005 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5659    2.6337    0.3034 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4359    1.0559   -1.1414 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7891   -0.7746   -1.6465 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1833   -0.8113    0.0401 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9566   -2.6525   -0.1987 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5418   -0.0979    0.1103 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7493   -2.0938    1.5161 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0308   -3.1701    0.3162 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3731   -2.7816   -0.1445 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3068   -2.2808   -1.5004 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6026    0.1075   -0.8630 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0916   -0.7635   -1.2775 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3169    1.6823    0.1568 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
  9 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
  1 24  1  0
  1 25  1  0
  1 26  1  0
  2 27  1  0
  2 28  1  0
  3 29  1  0
  3 30  1  0
  4 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
 10 39  1  0
 11 40  1  0
 12 41  1  0
 12 42  1  0
 13 43  1  0
 14 44  1  0
 15 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
 19 52  1  0
 20 53  1  0
 20 54  1  0
 23 55  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
12 Hydroxy arachidonate	Generator

Chemical Formula

C₂₀H₃₂O₃

Average Molecular Weight

320.4663

Monoisotopic Molecular Weight

320.23514489

IUPAC Name

(5E,8Z,11E,14Z)-12-hydroxyicosa-5,8,11,14-tetraenoic acid

Traditional Name

(5E,8Z,11E,14Z)-12-hydroxyicosa-5,8,11,14-tetraenoic acid

CAS Registry Number

Not Available

SMILES

CCCCC\C=C/C\C(O)=C/C\C=C/C\C=C\CCCC(O)=O

InChI Identifier

InChI=1S/C20H32O3/c1-2-3-4-5-10-13-16-19(21)17-14-11-8-6-7-9-12-15-18-20(22)23/h7-11,13,17,21H,2-6,12,14-16,18H2,1H3,(H,22,23)/b9-7+,11-8-,13-10-,19-17+

InChI Key

HVRRTPWRYUQZPF-RMOYYRCGSA-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
Hydroxy fatty acid
Unsaturated fatty acid
Monocarboxylic acid or derivatives
Enol
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Membrane (HMDB: HMDB0060101)

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	0.0016 g/L	ALOGPS
logP	6	ALOGPS
logP	5.76	ChemAxon
logS	-5.3	ALOGPS
pKa (Strongest Acidic)	4.82	ChemAxon
pKa (Strongest Basic)	-4.8	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	102 m³·mol⁻¹	ChemAxon
Polarizability	38.1 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	187.651	30932474
DeepCCS	[M-H]-	185.293	30932474
DeepCCS	[M-2H]-	218.179	30932474
DeepCCS	[M+Na]+	193.744	30932474
AllCCS	[M+H]+	186.6	32859911
AllCCS	[M+H-H2O]+	183.7	32859911
AllCCS	[M+NH4]+	189.2	32859911
AllCCS	[M+Na]+	190.0	32859911
AllCCS	[M-H]-	185.7	32859911
AllCCS	[M+Na-2H]-	187.5	32859911
AllCCS	[M+HCOO]-	189.6	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
12 Hydroxy arachidonic acid	CCCCC\C=C/C\C(O)=C/C\C=C/C\C=C\CCCC(O)=O	4087.4	Standard polar	33892256
12 Hydroxy arachidonic acid	CCCCC\C=C/C\C(O)=C/C\C=C/C\C=C\CCCC(O)=O	2349.0	Standard non polar	33892256
12 Hydroxy arachidonic acid	CCCCC\C=C/C\C(O)=C/C\C=C/C\C=C\CCCC(O)=O	2545.0	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
12 Hydroxy arachidonic acid,1TMS,isomer #1	CCCCC/C=C\C/C(=C\C/C=C\C/C=C/CCCC(=O)O)O[Si](C)(C)C	2722.4	Semi standard non polar	33892256
12 Hydroxy arachidonic acid,1TMS,isomer #2	CCCCC/C=C\C/C(O)=C\C/C=C\C/C=C/CCCC(=O)O[Si](C)(C)C	2580.6	Semi standard non polar	33892256
12 Hydroxy arachidonic acid,2TMS,isomer #1	CCCCC/C=C\C/C(=C\C/C=C\C/C=C/CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C	2659.2	Semi standard non polar	33892256
12 Hydroxy arachidonic acid,1TBDMS,isomer #1	CCCCC/C=C\C/C(=C\C/C=C\C/C=C/CCCC(=O)O)O[Si](C)(C)C(C)(C)C	2966.5	Semi standard non polar	33892256
12 Hydroxy arachidonic acid,1TBDMS,isomer #2	CCCCC/C=C\C/C(O)=C\C/C=C\C/C=C/CCCC(=O)O[Si](C)(C)C(C)(C)C	2828.2	Semi standard non polar	33892256
12 Hydroxy arachidonic acid,2TBDMS,isomer #1	CCCCC/C=C\C/C(=C\C/C=C\C/C=C/CCCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3164.5	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 - 12 Hydroxy arachidonic acid GC-MS (Non-derivatized) - 70eV, Positive	splash10-0007-7490000000-77f2c27f041aec75d04e	2017-09-20	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 12 Hydroxy arachidonic acid GC-MS (2 TMS) - 70eV, Positive	splash10-00b9-9124300000-aa0f245ea95c1aeb5ee7	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 12 Hydroxy arachidonic acid GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 12 Hydroxy arachidonic acid 10V, Positive-QTOF	splash10-0udi-0139000000-597464e971dfc31423d6	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 12 Hydroxy arachidonic acid 20V, Positive-QTOF	splash10-03fr-2931000000-b560ae06f02bc778f008	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 12 Hydroxy arachidonic acid 40V, Positive-QTOF	splash10-06rf-8940000000-816beaffaa8b3cb05313	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 12 Hydroxy arachidonic acid 10V, Negative-QTOF	splash10-014i-0019000000-25858efd6e393dfd014b	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 12 Hydroxy arachidonic acid 20V, Negative-QTOF	splash10-0n29-1879000000-377b30de875c39619d33	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 12 Hydroxy arachidonic acid 40V, Negative-QTOF	splash10-0a4i-9730000000-8aeb8db123286fab6a80	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 12 Hydroxy arachidonic acid 10V, Positive-QTOF	splash10-0fk9-2429000000-2c362c30c438ec300c21	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 12 Hydroxy arachidonic acid 20V, Positive-QTOF	splash10-0a4m-9811000000-ec8475538e017015d546	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 12 Hydroxy arachidonic acid 40V, Positive-QTOF	splash10-0aou-9400000000-a572091171de3d2f5555	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 12 Hydroxy arachidonic acid 10V, Negative-QTOF	splash10-014i-0209000000-65cd4c622adf9225f484	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 12 Hydroxy arachidonic acid 20V, Negative-QTOF	splash10-0gb9-0619000000-f40ac14b79b62887e8a9	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 12 Hydroxy arachidonic acid 40V, Negative-QTOF	splash10-052g-9781000000-9daa13be6af1689f01d3	2021-10-12	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Membrane (predicted from logP)

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

131769822

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

Thiele I, Swainston N, Fleming RM, Hoppe A, Sahoo S, Aurich MK, Haraldsdottir H, Mo ML, Rolfsson O, Stobbe MD, Thorleifsson SG, Agren R, Bolling C, Bordel S, Chavali AK, Dobson P, Dunn WB, Endler L, Hala D, Hucka M, Hull D, Jameson D, Jamshidi N, Jonsson JJ, Juty N, Keating S, Nookaew I, Le Novere N, Malys N, Mazein A, Papin JA, Price ND, Selkov E Sr, Sigurdsson MI, Simeonidis E, Sonnenschein N, Smallbone K, Sorokin A, van Beek JH, Weichart D, Goryanin I, Nielsen J, Westerhoff HV, Kell DB, Mendes P, Palsson BO: A community-driven global reconstruction of human metabolism. Nat Biotechnol. 2013 May;31(5):419-25. doi: 10.1038/nbt.2488. Epub 2013 Mar 3. [PubMed:23455439 ]
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 12 Hydroxy arachidonic acid (HMDB0060101)

MOL for HMDB0060101 (12 Hydroxy arachidonic acid)

3D MOL for HMDB0060101 (12 Hydroxy arachidonic acid)

3D SDF for HMDB0060101 (12 Hydroxy arachidonic acid)

3D-SDF for HMDB0060101 (12 Hydroxy arachidonic acid)

PDB for HMDB0060101 (12 Hydroxy arachidonic acid)

3D PDB for HMDB0060101 (12 Hydroxy arachidonic acid)

SMILES for HMDB0060101 (12 Hydroxy arachidonic acid)

INCHI for HMDB0060101 (12 Hydroxy arachidonic acid)

Structure for HMDB0060101 (12 Hydroxy arachidonic acid)

3D Structure for HMDB0060101 (12 Hydroxy arachidonic acid)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra