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83952-40-3

83952-40-3 Structure

83952-40-3 Structure
IdentificationBack Directory
[Name]

(+/-)5-HEPE
[CAS]

83952-40-3
[Synonyms]

(+/-)5-HEPE
(+/-)5-HEPE
FTAGQROYQYQRHF-FCWZHQICSA-N
5-hydroxy-6,8,11,14,17-eicosapentaenoic acid
(+/-)5-HYDROXYEICOSA-6E,8Z,11Z,14Z,17Z-PENTAENOIC ACID
(+/-)-5-HYDROXY-6E,8Z,11Z,14Z,17Z-EICOSAPENTAENOIC ACID
6,8,11,14,17-Eicosapentaenoic acid, 5-hydroxy-, (6E,8Z,11Z,14Z,17Z)-
[Molecular Formula]

C20H30O3
[MDL Number]

MFCD00171437
[MOL File]

83952-40-3.mol
[Molecular Weight]

318.45
Chemical PropertiesBack Directory
[Boiling point ]

488.0±45.0 °C(Predicted)
[density ]

0.997±0.06 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

0.1 M Na2CO3: 2 mg/ml; DMF: Miscible; DMSO: Miscible; Ethanol: Miscible; PBS pH 7.2: 0.8 mg/ml
[form ]

Clear to light-yellow liquid.
[pka]

4.67±0.10(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]


GHS02,GHS07
[Signal word ]

Danger
[Hazard statements ]

H225-H319
[Precautionary statements ]

P210-P233-P240-P241-P242-P243-P264-P280-P303+P361+P353-P305+P351+P338-P337+P313-P370+P378-P403+P235-P501
Hazard InformationBack Directory
[Description]

(±)5-HEPE is produced by non-enzymatic oxidation of EPA. It contains equal amounts of 5(S)-HEPE and 5(R)-HEPE. The biological activity of (±)5-HEPE is likely mediated by one of the individual isomers, most commonly the 5(S) isomer in mammalian systems. EPA can be metabolized to 5-HEPE in human and bovine neutrophils, and human eosinophils, which is further metabolized to 5-oxoEPE and LTB5. The 5-series metabolites of EPA, namely 5-HEPE, 5-oxoEPE, and LTB5, have significantly decreased biological effects compared to the arachidonic acid-derived metabolites.
[Definition]

ChEBI: 5-HEPE is a hydroxyicosapentaenoic acid that consists of 6E,8Z,11Z,14Z,17Z-icosapentaenoic acid with the hydroxy group located at position 5. It has a role as a mouse metabolite. It is a conjugate acid of a 5-HEPE(1-).
[storage]

Store at -20°C
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