Life Science

9(R)-HETE is an enantiomer which makes up 50% of (&plusmn)9-HETE (Item No. 34400). At a concentration of 300 nM, 9(R)-HETE activates RXR&gamma-dependent transcription 1.5 fold relative to a control.

9(R)-HETE is an enantiomer which makes up 50% of (&plusmn)9-HETE (Item No. 34400). At a concentration of 300 nM, 9(R)-HETE activates RXR&gamma-dependent transcription 1.5 fold relative to a control.

9(R)-HODE cholesteryl ester was originally extracted from atherosclerotic lesions. It remains uncertain whether the oxidized fatty acid portion of the molecule results from enzymatic lipoxygenation or from random lipid peroxidation.

9(R)-HODE cholesteryl ester was originally extracted from atherosclerotic lesions. It remains uncertain whether the oxidized fatty acid portion of the molecule results from enzymatic lipoxygenation or from random lipid peroxidation.

9(R)-HODE cholesteryl ester was originally extracted from atherosclerotic lesions. It remains uncertain whether the oxidized fatty acid portion of the molecule results from enzymatic lipoxygenation or from random lipid peroxidation.

9(R)-HODE is one of several monohydroxylated products of linoleic acid. All known mammalian lipoxygenases appear to catalyze the oxygenation of arachidonic and linoleic acid to give products having strictly the (S) configuration at the site of

9(R)-HODE is one of several monohydroxylated products of linoleic acid. All known mammalian lipoxygenases appear to catalyze the oxygenation of arachidonic and linoleic acid to give products having strictly the (S) configuration at the site of

9(R)-HODE is one of several monohydroxylated products of linoleic acid. All known mammalian lipoxygenases appear to catalyze the oxygenation of arachidonic and linoleic acid to give products having strictly the (S) configuration at the site of

9(R)-HODE is one of several monohydroxylated products of linoleic acid. All known mammalian lipoxygenases appear to catalyze the oxygenation of arachidonic and linoleic acid to give products having strictly the (S) configuration at the site of

A certified reference material that is structurally similar to known phytocannabinoids has been found as a byproduct in Cannabis processing potential impurity or degradant in preparations of ?9-THC,,

A purified enantiomer of (&plusmn)9-HETE resulting from non-enzymatic oxidation of arachidonic acid.

A purified enantiomer of (&plusmn)9-HETE resulting from non-enzymatic oxidation of arachidonic acid.