Biologically Active Small Molecules

An internal standard for the quantification of latanoprost by GC- or LC-mass spectrometry (MS).

An internal standard for the quantification of latanoprost by GC- or LC-mass spectrometry (MS).

An internal standard for the quantification of latanoprost by GC- or LC-mass spectrometry (MS).

An internal standard for the quantification of latanoprost by GC- or LC-mass spectrometry (MS).

(&plusmn)9-HEPE is produced by non-enzymatic oxidation of EPA. It contains equal amounts of 9(S)-HEPE and 9(R)-HEPE. The biological activity of (&plusmn)9-HEPE has not been clearly documented.

(&plusmn)9-HEPE is produced by non-enzymatic oxidation of EPA. It contains equal amounts of 9(S)-HEPE and 9(R)-HEPE. The biological activity of (&plusmn)9-HEPE has not been clearly documented.

(&plusmn)9-HEPE is produced by non-enzymatic oxidation of EPA. It contains equal amounts of 9(S)-HEPE and 9(R)-HEPE. The biological activity of (&plusmn)9-HEPE has not been clearly documented.

(&plusmn)9-HEPE is produced by non-enzymatic oxidation of EPA. It contains equal amounts of 9(S)-HEPE and 9(R)-HEPE. The biological activity of (&plusmn)9-HEPE has not been clearly documented.

(&plusmn)9-HETE is one of the six monohydroxy fatty acids produced by the non-enzymatic oxidation of arachidonic acid. The individual R and S isomers of racemic HETEs have been separated and identified using chiral phase HPLC.

(&plusmn)9-HETE is one of the six monohydroxy fatty acids produced by the non-enzymatic oxidation of arachidonic acid. The individual R and S isomers of racemic HETEs have been separated and identified using chiral phase HPLC.

(&plusmn)9-HETE is one of the six monohydroxy fatty acids produced by the non-enzymatic oxidation of arachidonic acid. The individual R and S isomers of racemic HETEs have been separated and identified using chiral phase HPLC.

(&plusmn)9-HETE is one of the six monohydroxy fatty acids produced by the non-enzymatic oxidation of arachidonic acid. The individual R and S isomers of racemic HETEs have been separated and identified using chiral phase HPLC.