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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 09:28:00 UTC

Update Date

2021-09-26 23:04:06 UTC

HMDB ID

HMDB0251839

Secondary Accession Numbers

None

Metabolite Identification

Common Name

Epi-Lipoxin A4

Description

5,6,15-trihydroxyicosa-7,9,11,13-tetraenoic acid belongs to the class of organic compounds known as lipoxins. These are eicosanoids with a trihydroxyicosatetraenoic acid skeleton (a c20-fatty acid, with the chain bearing three hydroxyl groups and four double bonds). Lipoxins have four double bonds, which are all conjugated. In some cases a hydroxyl group is substituted by a C=O group. Based on a literature review very few articles have been published on 5,6,15-trihydroxyicosa-7,9,11,13-tetraenoic acid. This compound has been identified in human blood as reported by (PMID: 31557052 ). Epi-lipoxin a4 is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically Epi-Lipoxin A4 is part of the human exposome. The exposome can be defined as the collection of all the exposures of an individual in a lifetime and how those exposures relate to health. An individual's exposure begins before birth and includes insults from environmental and occupational sources.

Structure

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

HMDB0251839
     RDKit          3D
Epi-Lipoxin A4
 57 56  0  0  0  0  0  0  0  0999 V2000
    6.8356    1.7150    2.7632 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0625    0.3266    2.2454 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3315    0.1636    0.9220 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5894   -1.2315    0.4518 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9196   -1.5151   -0.8517 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4058   -1.3548   -0.7679 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8810   -2.2405    0.1932 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8534   -1.6415   -2.1067 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5607   -1.4359   -2.3449 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7293   -0.9333   -1.2778 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4443   -0.7157   -1.4568 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2316   -0.9508   -2.6925 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5034   -0.7335   -2.8755 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3507   -0.2244   -1.8162 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6349   -0.0433   -2.1271 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5240    0.4810   -1.0495 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8182    1.4674   -0.3297 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9367   -0.6154   -0.1713 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8430   -1.1040    0.5696 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2254   -0.5775    0.4863 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6159    0.5038    1.3987 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8176    1.8648    0.8243 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2436    2.8134    1.9403 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3645    2.3880    3.1080 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4705    4.1195    1.5539 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7649    2.3162    2.6971 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0270    2.2498    2.2097 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5353    1.6623    3.8405 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1358    0.1032    2.0306 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6518   -0.4475    2.9291 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7132    0.8596    0.1548 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2775    0.4097    1.1174 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6794   -1.3520    0.3436 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1822   -1.9610    1.2126 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1487   -2.5045   -1.2555 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2624   -0.7353   -1.5886 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1792   -0.3280   -0.4220 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8275   -1.8209    1.0849 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4881   -2.0148   -2.8855 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1943   -1.6615   -3.3482 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1867   -0.7158   -0.2926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1069   -0.3308   -0.5816 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3107   -1.3372   -3.5681 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9322   -0.9494   -3.8745 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9572   -0.0152   -0.8598 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0715   -0.2443   -3.0832 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4043    1.0025   -1.5020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8560    2.3389   -0.8335 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0583   -1.5424   -0.9412 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9669   -0.8651    1.5393 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0606   -0.6530   -0.3289 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4437   -1.5984    1.0138 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5657    0.1921    1.9637 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8318    0.6119    2.2252 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6296    1.8469    0.0518 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9710    2.3457    0.3826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7421    4.6124    1.0375 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
  6  8  1  0
  8  9  2  3
  9 10  1  0
 10 11  2  3
 11 12  1  0
 12 13  2  3
 13 14  1  0
 14 15  2  3
 15 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
 18 20  1  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
  3 32  1  0
  4 33  1  0
  4 34  1  0
  5 35  1  0
  5 36  1  0
  6 37  1  0
  7 38  1  0
  8 39  1  0
  9 40  1  0
 10 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
 19 50  1  0
 20 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


  Mrv1652309112111282D          

 25 24  0  0  0  0            999 V2000
   -8.2421    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5276    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8131    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0987    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3842    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6697    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9552    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2408    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5263    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8118    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0974    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3829    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3316    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0461    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7605    1.8414    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
    3.1895    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9039    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6184    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3329    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0474    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3329    0.6039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4750    0.6039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7605    2.6664    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6697    0.6039    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
  7  6  1  4  0  0  0
  7  8  2  0  0  0  0
  9  8  1  4  0  0  0
  9 10  2  0  0  0  0
 11 10  1  4  0  0  0
 11 12  2  0  0  0  0
 13 12  1  4  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 16 23  1  0  0  0  0
 15 24  1  0  0  0  0
  6 25  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0251839

> <DATABASE_NAME>
hmdb

> <SMILES>
CCCCCC(O)C=CC=CC=CC=CC(O)C(O)CCCC(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C20H32O5/c1-2-3-8-12-17(21)13-9-6-4-5-7-10-14-18(22)19(23)15-11-16-20(24)25/h4-7,9-10,13-14,17-19,21-23H,2-3,8,11-12,15-16H2,1H3,(H,24,25)

> <INCHI_KEY>
IXAQOQZEOGMIQS-UHFFFAOYSA-N

> <FORMULA>
C20H32O5

> <MOLECULAR_WEIGHT>
352.471

> <EXACT_MASS>
352.22497413

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
57

> <JCHEM_AVERAGE_POLARIZABILITY>
42.03299512691871

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5,6,15-trihydroxyicosa-7,9,11,13-tetraenoic acid

> <ALOGPS_LOGP>
4.61

> <JCHEM_LOGP>
3.0506450699999985

> <ALOGPS_LOGS>
-3.90

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
13.658863253317975

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.475339418208748

> <JCHEM_PKA_STRONGEST_BASIC>
-1.575973533829957

> <JCHEM_POLAR_SURFACE_AREA>
97.99000000000001

> <JCHEM_REFRACTIVITY>
104.34649999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
14

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.41e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5,6,15-trihydroxyicosa-7,9,11,13-tetraenoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0251839
     RDKit          3D
Epi-Lipoxin A4
 57 56  0  0  0  0  0  0  0  0999 V2000
    6.8356    1.7150    2.7632 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0625    0.3266    2.2454 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3315    0.1636    0.9220 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5894   -1.2315    0.4518 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9196   -1.5151   -0.8517 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4058   -1.3548   -0.7679 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8810   -2.2405    0.1932 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8534   -1.6415   -2.1067 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5607   -1.4359   -2.3449 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7293   -0.9333   -1.2778 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4443   -0.7157   -1.4568 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2316   -0.9508   -2.6925 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5034   -0.7335   -2.8755 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3507   -0.2244   -1.8162 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6349   -0.0433   -2.1271 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5240    0.4810   -1.0495 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8182    1.4674   -0.3297 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9367   -0.6154   -0.1713 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8430   -1.1040    0.5696 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2254   -0.5775    0.4863 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6159    0.5038    1.3987 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8176    1.8648    0.8243 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2436    2.8134    1.9403 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3645    2.3880    3.1080 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4705    4.1195    1.5539 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7649    2.3162    2.6971 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0270    2.2498    2.2097 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5353    1.6623    3.8405 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1358    0.1032    2.0306 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6518   -0.4475    2.9291 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7132    0.8596    0.1548 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2775    0.4097    1.1174 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6794   -1.3520    0.3436 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1822   -1.9610    1.2126 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1487   -2.5045   -1.2555 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2624   -0.7353   -1.5886 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1792   -0.3280   -0.4220 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8275   -1.8209    1.0849 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4881   -2.0148   -2.8855 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1943   -1.6615   -3.3482 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1867   -0.7158   -0.2926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1069   -0.3308   -0.5816 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3107   -1.3372   -3.5681 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9322   -0.9494   -3.8745 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9572   -0.0152   -0.8598 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0715   -0.2443   -3.0832 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4043    1.0025   -1.5020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8560    2.3389   -0.8335 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0583   -1.5424   -0.9412 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9669   -0.8651    1.5393 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0606   -0.6530   -0.3289 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4437   -1.5984    1.0138 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5657    0.1921    1.9637 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8318    0.6119    2.2252 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6296    1.8469    0.0518 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9710    2.3457    0.3826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7421    4.6124    1.0375 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
  6  8  1  0
  8  9  2  3
  9 10  1  0
 10 11  2  3
 11 12  1  0
 12 13  2  3
 13 14  1  0
 14 15  2  3
 15 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
 18 20  1  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
  3 32  1  0
  4 33  1  0
  4 34  1  0
  5 35  1  0
  5 36  1  0
  6 37  1  0
  7 38  1  0
  8 39  1  0
  9 40  1  0
 10 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
 19 50  1  0
 20 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                                 11-SEP-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-21         0                                  
HETATM    1  C   UNK     0     -15.385   3.437   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -14.052   2.667   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -12.718   3.437   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0     -11.384   2.667   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0     -10.050   3.437   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -8.717   2.667   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -7.383   3.437   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -6.049   2.667   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -4.716   3.437   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -3.382   2.667   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.048   3.437   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.715   2.667   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.619   3.437   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.953   2.667   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.286   3.437   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       5.954   3.437   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.287   2.667   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.621   3.437   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.955   2.667   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      11.288   3.437   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       9.955   1.127   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       4.620   1.127   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       3.286   4.977   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0      -8.717   1.127   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   25                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   24                                                  
CONECT   16   15   17   23                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   16                                                            
CONECT   24   15                                                            
CONECT   25    6                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   48    0
END

COMPND    HMDB0251839
HETATM    1  C1  UNL     1       6.836   1.715   2.763  1.00  0.00           C  
HETATM    2  C2  UNL     1       7.062   0.327   2.245  1.00  0.00           C  
HETATM    3  C3  UNL     1       6.332   0.164   0.922  1.00  0.00           C  
HETATM    4  C4  UNL     1       6.589  -1.232   0.452  1.00  0.00           C  
HETATM    5  C5  UNL     1       5.920  -1.515  -0.852  1.00  0.00           C  
HETATM    6  C6  UNL     1       4.406  -1.355  -0.768  1.00  0.00           C  
HETATM    7  O1  UNL     1       3.881  -2.241   0.193  1.00  0.00           O  
HETATM    8  C7  UNL     1       3.853  -1.642  -2.107  1.00  0.00           C  
HETATM    9  C8  UNL     1       2.561  -1.436  -2.345  1.00  0.00           C  
HETATM   10  C9  UNL     1       1.729  -0.933  -1.278  1.00  0.00           C  
HETATM   11  C10 UNL     1       0.444  -0.716  -1.457  1.00  0.00           C  
HETATM   12  C11 UNL     1      -0.232  -0.951  -2.693  1.00  0.00           C  
HETATM   13  C12 UNL     1      -1.503  -0.734  -2.876  1.00  0.00           C  
HETATM   14  C13 UNL     1      -2.351  -0.224  -1.816  1.00  0.00           C  
HETATM   15  C14 UNL     1      -3.635  -0.043  -2.127  1.00  0.00           C  
HETATM   16  C15 UNL     1      -4.524   0.481  -1.050  1.00  0.00           C  
HETATM   17  O2  UNL     1      -3.818   1.467  -0.330  1.00  0.00           O  
HETATM   18  C16 UNL     1      -4.937  -0.615  -0.171  1.00  0.00           C  
HETATM   19  O3  UNL     1      -3.843  -1.104   0.570  1.00  0.00           O  
HETATM   20  C17 UNL     1      -6.225  -0.578   0.486  1.00  0.00           C  
HETATM   21  C18 UNL     1      -6.616   0.504   1.399  1.00  0.00           C  
HETATM   22  C19 UNL     1      -6.818   1.865   0.824  1.00  0.00           C  
HETATM   23  C20 UNL     1      -7.244   2.813   1.940  1.00  0.00           C  
HETATM   24  O4  UNL     1      -7.364   2.388   3.108  1.00  0.00           O  
HETATM   25  O5  UNL     1      -7.471   4.119   1.554  1.00  0.00           O  
HETATM   26  H1  UNL     1       7.765   2.316   2.697  1.00  0.00           H  
HETATM   27  H2  UNL     1       6.027   2.250   2.210  1.00  0.00           H  
HETATM   28  H3  UNL     1       6.535   1.662   3.841  1.00  0.00           H  
HETATM   29  H4  UNL     1       8.136   0.103   2.031  1.00  0.00           H  
HETATM   30  H5  UNL     1       6.652  -0.447   2.929  1.00  0.00           H  
HETATM   31  H6  UNL     1       6.713   0.860   0.155  1.00  0.00           H  
HETATM   32  H7  UNL     1       5.278   0.410   1.117  1.00  0.00           H  
HETATM   33  H8  UNL     1       7.679  -1.352   0.344  1.00  0.00           H  
HETATM   34  H9  UNL     1       6.182  -1.961   1.213  1.00  0.00           H  
HETATM   35  H10 UNL     1       6.149  -2.505  -1.256  1.00  0.00           H  
HETATM   36  H11 UNL     1       6.262  -0.735  -1.589  1.00  0.00           H  
HETATM   37  H12 UNL     1       4.179  -0.328  -0.422  1.00  0.00           H  
HETATM   38  H13 UNL     1       3.828  -1.821   1.085  1.00  0.00           H  
HETATM   39  H14 UNL     1       4.488  -2.015  -2.885  1.00  0.00           H  
HETATM   40  H15 UNL     1       2.194  -1.662  -3.348  1.00  0.00           H  
HETATM   41  H16 UNL     1       2.187  -0.716  -0.293  1.00  0.00           H  
HETATM   42  H17 UNL     1      -0.107  -0.331  -0.582  1.00  0.00           H  
HETATM   43  H18 UNL     1       0.311  -1.337  -3.568  1.00  0.00           H  
HETATM   44  H19 UNL     1      -1.932  -0.949  -3.874  1.00  0.00           H  
HETATM   45  H20 UNL     1      -1.957  -0.015  -0.860  1.00  0.00           H  
HETATM   46  H21 UNL     1      -4.071  -0.244  -3.083  1.00  0.00           H  
HETATM   47  H22 UNL     1      -5.404   1.003  -1.502  1.00  0.00           H  
HETATM   48  H23 UNL     1      -3.856   2.339  -0.834  1.00  0.00           H  
HETATM   49  H24 UNL     1      -5.058  -1.542  -0.941  1.00  0.00           H  
HETATM   50  H25 UNL     1      -3.967  -0.865   1.539  1.00  0.00           H  
HETATM   51  H26 UNL     1      -7.061  -0.653  -0.329  1.00  0.00           H  
HETATM   52  H27 UNL     1      -6.444  -1.598   1.014  1.00  0.00           H  
HETATM   53  H28 UNL     1      -7.566   0.192   1.964  1.00  0.00           H  
HETATM   54  H29 UNL     1      -5.832   0.612   2.225  1.00  0.00           H  
HETATM   55  H30 UNL     1      -7.630   1.847   0.052  1.00  0.00           H  
HETATM   56  H31 UNL     1      -5.971   2.346   0.383  1.00  0.00           H  
HETATM   57  H32 UNL     1      -6.742   4.612   1.037  1.00  0.00           H  
CONECT    1    2   26   27   28
CONECT    2    3   29   30
CONECT    3    4   31   32
CONECT    4    5   33   34
CONECT    5    6   35   36
CONECT    6    7    8   37
CONECT    7   38
CONECT    8    9    9   39
CONECT    9   10   40
CONECT   10   11   11   41
CONECT   11   12   42
CONECT   12   13   13   43
CONECT   13   14   44
CONECT   14   15   15   45
CONECT   15   16   46
CONECT   16   17   18   47
CONECT   17   48
CONECT   18   19   20   49
CONECT   19   50
CONECT   20   21   51   52
CONECT   21   22   53   54
CONECT   22   23   55   56
CONECT   23   24   24   25
CONECT   25   57
END

HMDB0251839
     RDKit          3D
Epi-Lipoxin A4
 57 56  0  0  0  0  0  0  0  0999 V2000
    6.8356    1.7150    2.7632 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0625    0.3266    2.2454 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3315    0.1636    0.9220 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5894   -1.2315    0.4518 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9196   -1.5151   -0.8517 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4058   -1.3548   -0.7679 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8810   -2.2405    0.1932 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8534   -1.6415   -2.1067 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5607   -1.4359   -2.3449 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7293   -0.9333   -1.2778 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4443   -0.7157   -1.4568 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2316   -0.9508   -2.6925 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5034   -0.7335   -2.8755 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3507   -0.2244   -1.8162 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6349   -0.0433   -2.1271 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5240    0.4810   -1.0495 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8182    1.4674   -0.3297 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9367   -0.6154   -0.1713 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8430   -1.1040    0.5696 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2254   -0.5775    0.4863 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6159    0.5038    1.3987 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8176    1.8648    0.8243 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2436    2.8134    1.9403 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3645    2.3880    3.1080 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4705    4.1195    1.5539 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7649    2.3162    2.6971 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0270    2.2498    2.2097 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5353    1.6623    3.8405 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1358    0.1032    2.0306 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6518   -0.4475    2.9291 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7132    0.8596    0.1548 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2775    0.4097    1.1174 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6794   -1.3520    0.3436 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1822   -1.9610    1.2126 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1487   -2.5045   -1.2555 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2624   -0.7353   -1.5886 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1792   -0.3280   -0.4220 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8275   -1.8209    1.0849 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4881   -2.0148   -2.8855 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1943   -1.6615   -3.3482 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1867   -0.7158   -0.2926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1069   -0.3308   -0.5816 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3107   -1.3372   -3.5681 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9322   -0.9494   -3.8745 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9572   -0.0152   -0.8598 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0715   -0.2443   -3.0832 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4043    1.0025   -1.5020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8560    2.3389   -0.8335 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0583   -1.5424   -0.9412 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9669   -0.8651    1.5393 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0606   -0.6530   -0.3289 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4437   -1.5984    1.0138 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5657    0.1921    1.9637 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8318    0.6119    2.2252 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6296    1.8469    0.0518 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9710    2.3457    0.3826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7421    4.6124    1.0375 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
  6  8  1  0
  8  9  2  3
  9 10  1  0
 10 11  2  3
 11 12  1  0
 12 13  2  3
 13 14  1  0
 14 15  2  3
 15 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
 18 20  1  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
  3 32  1  0
  4 33  1  0
  4 34  1  0
  5 35  1  0
  5 36  1  0
  6 37  1  0
  7 38  1  0
  8 39  1  0
  9 40  1  0
 10 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
 19 50  1  0
 20 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
5,6,15-Trihydroxyicosa-7,9,11,13-tetraenoate	Generator

Chemical Formula

C₂₀H₃₂O₅

Average Molecular Weight

352.471

Monoisotopic Molecular Weight

352.22497413

IUPAC Name

5,6,15-trihydroxyicosa-7,9,11,13-tetraenoic acid

Traditional Name

5,6,15-trihydroxyicosa-7,9,11,13-tetraenoic acid

CAS Registry Number

Not Available

SMILES

CCCCCC(O)C=CC=CC=CC=CC(O)C(O)CCCC(O)=O

InChI Identifier

InChI=1S/C20H32O5/c1-2-3-8-12-17(21)13-9-6-4-5-7-10-14-18(22)19(23)15-11-16-20(24)25/h4-7,9-10,13-14,17-19,21-23H,2-3,8,11-12,15-16H2,1H3,(H,24,25)

InChI Key

IXAQOQZEOGMIQS-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as lipoxins. These are eicosanoids with a trihydroxyicosatetraenoic acid skeleton (a c20-fatty acid, with the chain bearing three hydroxyl groups and four double bonds). Lipoxins have four double bonds, which are all conjugated. In some cases a hydroxyl group is substituted by a C=O group.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Eicosanoids

Direct Parent

Lipoxins

Alternative Parents

Substituents

Lipoxin
Long-chain fatty acid
Hydroxy fatty acid
Fatty acid
Unsaturated fatty acid
Secondary alcohol
Carboxylic acid derivative
Carboxylic acid
Monocarboxylic acid or derivatives
Polyol
Organic oxide
Organic oxygen compound
Hydrocarbon derivative
Carbonyl group
Organooxygen compound
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: 31557052)

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
logP	4.61	ALOGPS
logP	3.05	ChemAxon
logS	-3.9	ALOGPS
pKa (Strongest Acidic)	4.48	ChemAxon
pKa (Strongest Basic)	-1.6	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	97.99 Å²	ChemAxon
Rotatable Bond Count	14	ChemAxon
Refractivity	104.35 m³·mol⁻¹	ChemAxon
Polarizability	42.03 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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
DeepCCS	[M+H]+	189.089	30932474
DeepCCS	[M-H]-	186.731	30932474
DeepCCS	[M-2H]-	219.617	30932474
DeepCCS	[M+Na]+	195.182	30932474

Predicted Kovats Retention Indices

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Epi-Lipoxin A4,1TMS,isomer #1	CCCCCC(C=CC=CC=CC=CC(O)C(O)CCCC(=O)O)O[Si](C)(C)C	3191.2	Semi standard non polar	33892256
Epi-Lipoxin A4,1TMS,isomer #1	CCCCCC(C=CC=CC=CC=CC(O)C(O)CCCC(=O)O)O[Si](C)(C)C	2877.7	Standard non polar	33892256
Epi-Lipoxin A4,1TMS,isomer #1	CCCCCC(C=CC=CC=CC=CC(O)C(O)CCCC(=O)O)O[Si](C)(C)C	3882.4	Standard polar	33892256
Epi-Lipoxin A4,1TMS,isomer #2	CCCCCC(O)C=CC=CC=CC=CC(O[Si](C)(C)C)C(O)CCCC(=O)O	3166.7	Semi standard non polar	33892256
Epi-Lipoxin A4,1TMS,isomer #2	CCCCCC(O)C=CC=CC=CC=CC(O[Si](C)(C)C)C(O)CCCC(=O)O	2860.6	Standard non polar	33892256
Epi-Lipoxin A4,1TMS,isomer #2	CCCCCC(O)C=CC=CC=CC=CC(O[Si](C)(C)C)C(O)CCCC(=O)O	3876.0	Standard polar	33892256
Epi-Lipoxin A4,1TMS,isomer #3	CCCCCC(O)C=CC=CC=CC=CC(O)C(CCCC(=O)O)O[Si](C)(C)C	3157.4	Semi standard non polar	33892256
Epi-Lipoxin A4,1TMS,isomer #3	CCCCCC(O)C=CC=CC=CC=CC(O)C(CCCC(=O)O)O[Si](C)(C)C	2876.3	Standard non polar	33892256
Epi-Lipoxin A4,1TMS,isomer #3	CCCCCC(O)C=CC=CC=CC=CC(O)C(CCCC(=O)O)O[Si](C)(C)C	3922.0	Standard polar	33892256
Epi-Lipoxin A4,1TMS,isomer #4	CCCCCC(O)C=CC=CC=CC=CC(O)C(O)CCCC(=O)O[Si](C)(C)C	3086.5	Semi standard non polar	33892256
Epi-Lipoxin A4,1TMS,isomer #4	CCCCCC(O)C=CC=CC=CC=CC(O)C(O)CCCC(=O)O[Si](C)(C)C	2897.5	Standard non polar	33892256
Epi-Lipoxin A4,1TMS,isomer #4	CCCCCC(O)C=CC=CC=CC=CC(O)C(O)CCCC(=O)O[Si](C)(C)C	3964.5	Standard polar	33892256
Epi-Lipoxin A4,2TMS,isomer #1	CCCCCC(C=CC=CC=CC=CC(O[Si](C)(C)C)C(O)CCCC(=O)O)O[Si](C)(C)C	3189.2	Semi standard non polar	33892256
Epi-Lipoxin A4,2TMS,isomer #1	CCCCCC(C=CC=CC=CC=CC(O[Si](C)(C)C)C(O)CCCC(=O)O)O[Si](C)(C)C	2858.3	Standard non polar	33892256
Epi-Lipoxin A4,2TMS,isomer #1	CCCCCC(C=CC=CC=CC=CC(O[Si](C)(C)C)C(O)CCCC(=O)O)O[Si](C)(C)C	3573.6	Standard polar	33892256
Epi-Lipoxin A4,2TMS,isomer #2	CCCCCC(C=CC=CC=CC=CC(O)C(CCCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C	3182.7	Semi standard non polar	33892256
Epi-Lipoxin A4,2TMS,isomer #2	CCCCCC(C=CC=CC=CC=CC(O)C(CCCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C	2886.2	Standard non polar	33892256
Epi-Lipoxin A4,2TMS,isomer #2	CCCCCC(C=CC=CC=CC=CC(O)C(CCCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C	3602.1	Standard polar	33892256
Epi-Lipoxin A4,2TMS,isomer #3	CCCCCC(C=CC=CC=CC=CC(O)C(O)CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C	3103.6	Semi standard non polar	33892256
Epi-Lipoxin A4,2TMS,isomer #3	CCCCCC(C=CC=CC=CC=CC(O)C(O)CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C	2915.3	Standard non polar	33892256
Epi-Lipoxin A4,2TMS,isomer #3	CCCCCC(C=CC=CC=CC=CC(O)C(O)CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C	3611.0	Standard polar	33892256
Epi-Lipoxin A4,2TMS,isomer #4	CCCCCC(O)C=CC=CC=CC=CC(O[Si](C)(C)C)C(CCCC(=O)O)O[Si](C)(C)C	3174.4	Semi standard non polar	33892256
Epi-Lipoxin A4,2TMS,isomer #4	CCCCCC(O)C=CC=CC=CC=CC(O[Si](C)(C)C)C(CCCC(=O)O)O[Si](C)(C)C	2864.0	Standard non polar	33892256
Epi-Lipoxin A4,2TMS,isomer #4	CCCCCC(O)C=CC=CC=CC=CC(O[Si](C)(C)C)C(CCCC(=O)O)O[Si](C)(C)C	3585.2	Standard polar	33892256
Epi-Lipoxin A4,2TMS,isomer #5	CCCCCC(O)C=CC=CC=CC=CC(O[Si](C)(C)C)C(O)CCCC(=O)O[Si](C)(C)C	3084.4	Semi standard non polar	33892256
Epi-Lipoxin A4,2TMS,isomer #5	CCCCCC(O)C=CC=CC=CC=CC(O[Si](C)(C)C)C(O)CCCC(=O)O[Si](C)(C)C	2896.8	Standard non polar	33892256
Epi-Lipoxin A4,2TMS,isomer #5	CCCCCC(O)C=CC=CC=CC=CC(O[Si](C)(C)C)C(O)CCCC(=O)O[Si](C)(C)C	3634.0	Standard polar	33892256
Epi-Lipoxin A4,2TMS,isomer #6	CCCCCC(O)C=CC=CC=CC=CC(O)C(CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C	3095.4	Semi standard non polar	33892256
Epi-Lipoxin A4,2TMS,isomer #6	CCCCCC(O)C=CC=CC=CC=CC(O)C(CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C	2920.3	Standard non polar	33892256
Epi-Lipoxin A4,2TMS,isomer #6	CCCCCC(O)C=CC=CC=CC=CC(O)C(CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C	3653.3	Standard polar	33892256
Epi-Lipoxin A4,3TMS,isomer #1	CCCCCC(C=CC=CC=CC=CC(O[Si](C)(C)C)C(CCCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C	3146.2	Semi standard non polar	33892256
Epi-Lipoxin A4,3TMS,isomer #1	CCCCCC(C=CC=CC=CC=CC(O[Si](C)(C)C)C(CCCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C	2828.2	Standard non polar	33892256
Epi-Lipoxin A4,3TMS,isomer #1	CCCCCC(C=CC=CC=CC=CC(O[Si](C)(C)C)C(CCCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C	3322.7	Standard polar	33892256
Epi-Lipoxin A4,3TMS,isomer #2	CCCCCC(C=CC=CC=CC=CC(O[Si](C)(C)C)C(O)CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C	3079.4	Semi standard non polar	33892256
Epi-Lipoxin A4,3TMS,isomer #2	CCCCCC(C=CC=CC=CC=CC(O[Si](C)(C)C)C(O)CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C	2857.0	Standard non polar	33892256
Epi-Lipoxin A4,3TMS,isomer #2	CCCCCC(C=CC=CC=CC=CC(O[Si](C)(C)C)C(O)CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C	3368.5	Standard polar	33892256
Epi-Lipoxin A4,3TMS,isomer #3	CCCCCC(C=CC=CC=CC=CC(O)C(CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	3088.1	Semi standard non polar	33892256
Epi-Lipoxin A4,3TMS,isomer #3	CCCCCC(C=CC=CC=CC=CC(O)C(CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	2885.7	Standard non polar	33892256
Epi-Lipoxin A4,3TMS,isomer #3	CCCCCC(C=CC=CC=CC=CC(O)C(CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	3371.5	Standard polar	33892256
Epi-Lipoxin A4,3TMS,isomer #4	CCCCCC(O)C=CC=CC=CC=CC(O[Si](C)(C)C)C(CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C	3091.0	Semi standard non polar	33892256
Epi-Lipoxin A4,3TMS,isomer #4	CCCCCC(O)C=CC=CC=CC=CC(O[Si](C)(C)C)C(CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C	2878.1	Standard non polar	33892256
Epi-Lipoxin A4,3TMS,isomer #4	CCCCCC(O)C=CC=CC=CC=CC(O[Si](C)(C)C)C(CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C	3356.4	Standard polar	33892256
Epi-Lipoxin A4,4TMS,isomer #1	CCCCCC(C=CC=CC=CC=CC(O[Si](C)(C)C)C(CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	3067.9	Semi standard non polar	33892256
Epi-Lipoxin A4,4TMS,isomer #1	CCCCCC(C=CC=CC=CC=CC(O[Si](C)(C)C)C(CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	2858.3	Standard non polar	33892256
Epi-Lipoxin A4,4TMS,isomer #1	CCCCCC(C=CC=CC=CC=CC(O[Si](C)(C)C)C(CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	3113.2	Standard polar	33892256
Epi-Lipoxin A4,1TBDMS,isomer #1	CCCCCC(C=CC=CC=CC=CC(O)C(O)CCCC(=O)O)O[Si](C)(C)C(C)(C)C	3427.5	Semi standard non polar	33892256
Epi-Lipoxin A4,1TBDMS,isomer #1	CCCCCC(C=CC=CC=CC=CC(O)C(O)CCCC(=O)O)O[Si](C)(C)C(C)(C)C	3073.7	Standard non polar	33892256
Epi-Lipoxin A4,1TBDMS,isomer #1	CCCCCC(C=CC=CC=CC=CC(O)C(O)CCCC(=O)O)O[Si](C)(C)C(C)(C)C	3920.2	Standard polar	33892256
Epi-Lipoxin A4,1TBDMS,isomer #2	CCCCCC(O)C=CC=CC=CC=CC(O[Si](C)(C)C(C)(C)C)C(O)CCCC(=O)O	3412.7	Semi standard non polar	33892256
Epi-Lipoxin A4,1TBDMS,isomer #2	CCCCCC(O)C=CC=CC=CC=CC(O[Si](C)(C)C(C)(C)C)C(O)CCCC(=O)O	3066.0	Standard non polar	33892256
Epi-Lipoxin A4,1TBDMS,isomer #2	CCCCCC(O)C=CC=CC=CC=CC(O[Si](C)(C)C(C)(C)C)C(O)CCCC(=O)O	3923.9	Standard polar	33892256
Epi-Lipoxin A4,1TBDMS,isomer #3	CCCCCC(O)C=CC=CC=CC=CC(O)C(CCCC(=O)O)O[Si](C)(C)C(C)(C)C	3401.4	Semi standard non polar	33892256
Epi-Lipoxin A4,1TBDMS,isomer #3	CCCCCC(O)C=CC=CC=CC=CC(O)C(CCCC(=O)O)O[Si](C)(C)C(C)(C)C	3090.6	Standard non polar	33892256
Epi-Lipoxin A4,1TBDMS,isomer #3	CCCCCC(O)C=CC=CC=CC=CC(O)C(CCCC(=O)O)O[Si](C)(C)C(C)(C)C	3956.5	Standard polar	33892256
Epi-Lipoxin A4,1TBDMS,isomer #4	CCCCCC(O)C=CC=CC=CC=CC(O)C(O)CCCC(=O)O[Si](C)(C)C(C)(C)C	3329.8	Semi standard non polar	33892256
Epi-Lipoxin A4,1TBDMS,isomer #4	CCCCCC(O)C=CC=CC=CC=CC(O)C(O)CCCC(=O)O[Si](C)(C)C(C)(C)C	3100.4	Standard non polar	33892256
Epi-Lipoxin A4,1TBDMS,isomer #4	CCCCCC(O)C=CC=CC=CC=CC(O)C(O)CCCC(=O)O[Si](C)(C)C(C)(C)C	3968.6	Standard polar	33892256
Epi-Lipoxin A4,2TBDMS,isomer #1	CCCCCC(C=CC=CC=CC=CC(O[Si](C)(C)C(C)(C)C)C(O)CCCC(=O)O)O[Si](C)(C)C(C)(C)C	3642.6	Semi standard non polar	33892256
Epi-Lipoxin A4,2TBDMS,isomer #1	CCCCCC(C=CC=CC=CC=CC(O[Si](C)(C)C(C)(C)C)C(O)CCCC(=O)O)O[Si](C)(C)C(C)(C)C	3286.1	Standard non polar	33892256
Epi-Lipoxin A4,2TBDMS,isomer #1	CCCCCC(C=CC=CC=CC=CC(O[Si](C)(C)C(C)(C)C)C(O)CCCC(=O)O)O[Si](C)(C)C(C)(C)C	3702.0	Standard polar	33892256
Epi-Lipoxin A4,2TBDMS,isomer #2	CCCCCC(C=CC=CC=CC=CC(O)C(CCCC(=O)O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3641.7	Semi standard non polar	33892256
Epi-Lipoxin A4,2TBDMS,isomer #2	CCCCCC(C=CC=CC=CC=CC(O)C(CCCC(=O)O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3330.1	Standard non polar	33892256
Epi-Lipoxin A4,2TBDMS,isomer #2	CCCCCC(C=CC=CC=CC=CC(O)C(CCCC(=O)O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3719.0	Standard polar	33892256
Epi-Lipoxin A4,2TBDMS,isomer #3	CCCCCC(C=CC=CC=CC=CC(O)C(O)CCCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3602.8	Semi standard non polar	33892256
Epi-Lipoxin A4,2TBDMS,isomer #3	CCCCCC(C=CC=CC=CC=CC(O)C(O)CCCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3331.5	Standard non polar	33892256
Epi-Lipoxin A4,2TBDMS,isomer #3	CCCCCC(C=CC=CC=CC=CC(O)C(O)CCCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3718.5	Standard polar	33892256
Epi-Lipoxin A4,2TBDMS,isomer #4	CCCCCC(O)C=CC=CC=CC=CC(O[Si](C)(C)C(C)(C)C)C(CCCC(=O)O)O[Si](C)(C)C(C)(C)C	3639.6	Semi standard non polar	33892256
Epi-Lipoxin A4,2TBDMS,isomer #4	CCCCCC(O)C=CC=CC=CC=CC(O[Si](C)(C)C(C)(C)C)C(CCCC(=O)O)O[Si](C)(C)C(C)(C)C	3316.4	Standard non polar	33892256
Epi-Lipoxin A4,2TBDMS,isomer #4	CCCCCC(O)C=CC=CC=CC=CC(O[Si](C)(C)C(C)(C)C)C(CCCC(=O)O)O[Si](C)(C)C(C)(C)C	3708.3	Standard polar	33892256
Epi-Lipoxin A4,2TBDMS,isomer #5	CCCCCC(O)C=CC=CC=CC=CC(O[Si](C)(C)C(C)(C)C)C(O)CCCC(=O)O[Si](C)(C)C(C)(C)C	3577.2	Semi standard non polar	33892256
Epi-Lipoxin A4,2TBDMS,isomer #5	CCCCCC(O)C=CC=CC=CC=CC(O[Si](C)(C)C(C)(C)C)C(O)CCCC(=O)O[Si](C)(C)C(C)(C)C	3328.8	Standard non polar	33892256
Epi-Lipoxin A4,2TBDMS,isomer #5	CCCCCC(O)C=CC=CC=CC=CC(O[Si](C)(C)C(C)(C)C)C(O)CCCC(=O)O[Si](C)(C)C(C)(C)C	3740.5	Standard polar	33892256
Epi-Lipoxin A4,2TBDMS,isomer #6	CCCCCC(O)C=CC=CC=CC=CC(O)C(CCCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3583.1	Semi standard non polar	33892256
Epi-Lipoxin A4,2TBDMS,isomer #6	CCCCCC(O)C=CC=CC=CC=CC(O)C(CCCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3368.1	Standard non polar	33892256
Epi-Lipoxin A4,2TBDMS,isomer #6	CCCCCC(O)C=CC=CC=CC=CC(O)C(CCCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3749.6	Standard polar	33892256
Epi-Lipoxin A4,3TBDMS,isomer #1	CCCCCC(C=CC=CC=CC=CC(O[Si](C)(C)C(C)(C)C)C(CCCC(=O)O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3873.9	Semi standard non polar	33892256
Epi-Lipoxin A4,3TBDMS,isomer #1	CCCCCC(C=CC=CC=CC=CC(O[Si](C)(C)C(C)(C)C)C(CCCC(=O)O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3460.1	Standard non polar	33892256
Epi-Lipoxin A4,3TBDMS,isomer #1	CCCCCC(C=CC=CC=CC=CC(O[Si](C)(C)C(C)(C)C)C(CCCC(=O)O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3514.8	Standard polar	33892256
Epi-Lipoxin A4,3TBDMS,isomer #2	CCCCCC(C=CC=CC=CC=CC(O[Si](C)(C)C(C)(C)C)C(O)CCCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3836.2	Semi standard non polar	33892256
Epi-Lipoxin A4,3TBDMS,isomer #2	CCCCCC(C=CC=CC=CC=CC(O[Si](C)(C)C(C)(C)C)C(O)CCCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3481.4	Standard non polar	33892256
Epi-Lipoxin A4,3TBDMS,isomer #2	CCCCCC(C=CC=CC=CC=CC(O[Si](C)(C)C(C)(C)C)C(O)CCCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3558.0	Standard polar	33892256
Epi-Lipoxin A4,3TBDMS,isomer #3	CCCCCC(C=CC=CC=CC=CC(O)C(CCCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3842.0	Semi standard non polar	33892256
Epi-Lipoxin A4,3TBDMS,isomer #3	CCCCCC(C=CC=CC=CC=CC(O)C(CCCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3516.4	Standard non polar	33892256
Epi-Lipoxin A4,3TBDMS,isomer #3	CCCCCC(C=CC=CC=CC=CC(O)C(CCCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3548.3	Standard polar	33892256
Epi-Lipoxin A4,3TBDMS,isomer #4	CCCCCC(O)C=CC=CC=CC=CC(O[Si](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	3837.4	Semi standard non polar	33892256
Epi-Lipoxin A4,3TBDMS,isomer #4	CCCCCC(O)C=CC=CC=CC=CC(O[Si](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	3510.2	Standard non polar	33892256
Epi-Lipoxin A4,3TBDMS,isomer #4	CCCCCC(O)C=CC=CC=CC=CC(O[Si](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	3541.6	Standard polar	33892256
Epi-Lipoxin A4,4TBDMS,isomer #1	CCCCCC(C=CC=CC=CC=CC(O[Si](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)O[Si](C)(C)C(C)(C)C	4060.8	Semi standard non polar	33892256
Epi-Lipoxin A4,4TBDMS,isomer #1	CCCCCC(C=CC=CC=CC=CC(O[Si](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)O[Si](C)(C)C(C)(C)C	3670.5	Standard non polar	33892256
Epi-Lipoxin A4,4TBDMS,isomer #1	CCCCCC(C=CC=CC=CC=CC(O[Si](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)O[Si](C)(C)C(C)(C)C	3342.6	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Epi-Lipoxin A4 GC-MS (Non-derivatized) - 70eV, Positive	splash10-02ti-3942000000-539dee31c556f111beef	2021-09-24	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Epi-Lipoxin A4 GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Epi-Lipoxin A4 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 - Epi-Lipoxin A4 10V, Positive-QTOF	splash10-014r-0119000000-31a93937ad49974a814e	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Epi-Lipoxin A4 20V, Positive-QTOF	splash10-00kr-1936000000-0ece3e36fd898b1f9097	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Epi-Lipoxin A4 40V, Positive-QTOF	splash10-059f-9600000000-18d8014a43feca3a38b6	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Epi-Lipoxin A4 10V, Negative-QTOF	splash10-0ue9-0009000000-cb99b6286e5f411abaa3	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Epi-Lipoxin A4 20V, Negative-QTOF	splash10-0gc0-4459000000-b29437cc7614015ca29b	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Epi-Lipoxin A4 40V, Negative-QTOF	splash10-014j-9320000000-477457ab7d09daaade6b	2021-10-12	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

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 but not Quantified	Not Quantified	Not Specified	Not Specified	Normal	31557052	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

3797

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

3934

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

Barupal DK, Fiehn O: Generating the Blood Exposome Database Using a Comprehensive Text Mining and Database Fusion Approach. Environ Health Perspect. 2019 Sep;127(9):97008. doi: 10.1289/EHP4713. Epub 2019 Sep 26. [PubMed:31557052 ]

Showing metabocard for Epi-Lipoxin A4 (HMDB0251839)

MOL for HMDB0251839 (Epi-Lipoxin A4)

3D MOL for HMDB0251839 (Epi-Lipoxin A4)

3D SDF for HMDB0251839 (Epi-Lipoxin A4)

3D-SDF for HMDB0251839 (Epi-Lipoxin A4)

PDB for HMDB0251839 (Epi-Lipoxin A4)

3D PDB for HMDB0251839 (Epi-Lipoxin A4)

SMILES for HMDB0251839 (Epi-Lipoxin A4)

INCHI for HMDB0251839 (Epi-Lipoxin A4)

Structure for HMDB0251839 (Epi-Lipoxin A4)

3D Structure for HMDB0251839 (Epi-Lipoxin A4)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Derivatized

GC-MS Spectra

MS/MS Spectra