Lipids

(±)18-HEPE is produced by non-enzymatic oxidation of EPA. It contains equal amounts of 18(S)-HEPE and 18(R)-HEPE. Specific biological activity attributed to (±)18-HEPE has not been documented.

(±)18-HEPE is produced by non-enzymatic oxidation of EPA. It contains equal amounts of 18(S)-HEPE and 18(R)-HEPE. Specific biological activity attributed to (±)18-HEPE has not been documented.

(±)20-HDoHE is an autoxidation product of docosahexaenoic acid (DHA) in vitro. Also, it is produced from incubations of DHA in rat brain, intestinal and liver microsomes. It is a potential marker of oxidative stress in brain and retina where DHA is

(±)20-HDoHE is an autoxidation product of docosahexaenoic acid (DHA) in vitro. Also, it is produced from incubations of DHA in rat brain, intestinal and liver microsomes. It is a potential marker of oxidative stress in brain and retina where DHA is

(±)4-HDoHE is an autoxidation product of docosahexaenoic acid (DHA)|in vitro|. It has been found to be produced from incubations of DHA in rat brain, intestinal microsomes and liver. (±)4-HDoHE may serve as a potential marker of oxidative stress in

(±)4-HDoHE is an autoxidation product of docosahexaenoic acid (DHA)|in vitro|. It has been found to be produced from incubations of DHA in rat brain, intestinal microsomes and liver. (±)4-HDoHE may serve as a potential marker of oxidative stress in

Product DescriptionEpoxide hydrolases convert the EETs into vicinal diols, with concurrent loss of much of their biological activity. It is a substrate for sheep seminal vesicle COX, producing 5,6-dihydroxy prostaglandin E1 and F1α metabolites in

Product DescriptionEpoxide hydrolases convert the EETs into vicinal diols, with concurrent loss of much of their biological activity. It is a substrate for sheep seminal vesicle COX, producing 5,6-dihydroxy prostaglandin E1 and F1α metabolites in

Epoxide hydrolases convert EETs into vicinal diols, with concurrent loss of their biological activity. (±)5,(6)-DHET can be transformed to the 1,5-lactone as an artifact during extraction.

Epoxide hydrolases convert EETs into vicinal diols, with concurrent loss of their biological activity. (±)5,(6)-DHET can be transformed to the 1,5-lactone as an artifact during extraction.

Produced by non-enzymatic oxidation of EPA resulting in a racemic mixture of 5-HEPE. The biological activity 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

Produced by non-enzymatic oxidation of EPA resulting in a racemic mixture of 5-HEPE. The biological activity 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