Laboratory

A DHA epoxygenase metabolite detected in rat brain and spinal cord, as well as human serum, that acts as a substrate for sEH (Km = 5.1 &microM) demonstrates antihyperalgesic activity in inflammatory and neuropathic pain models and potently

A DHA epoxygenase metabolite detected in rat brain and spinal cord, as well as human serum, that acts as a substrate for sEH (Km = 5.1 &microM) demonstrates antihyperalgesic activity in inflammatory and neuropathic pain models and potently

(&plusmn)10-HDHA is an autoxidation product of DHA in vitro. It is also produced from incubations of DHA in rat liver, brain, and intestinal microsomes.

(&plusmn)10-HDHA is an autoxidation product of DHA in vitro. It is also produced from incubations of DHA in rat liver, brain, and intestinal microsomes.

(&plusmn)10-HDHA is an autoxidation product of DHA in vitro. It is also produced from incubations of DHA in rat liver, brain, and intestinal microsomes.

(&plusmn)10-HDHA is an autoxidation product of DHA in vitro. It is also produced from incubations of DHA in rat liver, brain, and intestinal microsomes.

An internal standard for the quantification of (&plusmn)11(12)-DHET by GC- or LC-MS.

An internal standard for the quantification of (&plusmn)11(12)-DHET by GC- or LC-MS.

An internal standard for the quantification of (&plusmn)11(12)-DHET by GC- or LC-MS.

An internal standard for the quantification of (&plusmn)11(12)-DHET by GC- or LC-MS.

The diol resulting from the sEH opening of (&plusmn)11(12)-EET contracts artery rings with approximately 70% of the magnitude of (&plusmn)11(12)-EET.

The diol resulting from the sEH opening of (&plusmn)11(12)-EET contracts artery rings with approximately 70% of the magnitude of (&plusmn)11(12)-EET.