ligands acting on targets

15(S)-15-methyl Prostaglandin F2α is a metabolically stable analog of PGF2α. It is a potent uterine stimulant and abortifacient which can be given intramuscularly to induce labor. It induces luteolysis and reduces serum progesterone concentrations

15(S)-15-methyl Prostaglandin F2α methyl ester is a derivative of 15(S)-15-methyl PGF2α with increased membrane permeability.

15(S)-15-methyl Prostaglandin F2α methyl ester is a derivative of 15(S)-15-methyl PGF2α with increased membrane permeability.

15(S)-15-methyl Prostaglandin F2α methyl ester is a derivative of 15(S)-15-methyl PGF2α with increased membrane permeability.

(+)-15(R)-Fluprostenol isopropyl ester is a prodrug (Travoprost) which is converted by esterase enzymatic activity in the cornea to yield the corresponding free acid. The free acid, (+)-15(R)-fluprostenol, is a potent FP receptor agonist. The

(+)-15(R)-Fluprostenol isopropyl ester is a prodrug (Travoprost) which is converted by esterase enzymatic activity in the cornea to yield the corresponding free acid. The free acid, (+)-15(R)-fluprostenol, is a potent FP receptor agonist. The

15(S)-HEDE has been identified in psoriatic skin scale extracts (undetermined 15-OH stereochemistry) and inhibits 5-LO (5-lipoxygenase) with an IC|50|of 26 μM.

15(S)-HEDE has been identified in psoriatic skin scale extracts (undetermined 15-OH stereochemistry) and inhibits 5-LO (5-lipoxygenase) with an IC|50|of 26 μM.

15(S)-HEDE has been identified in psoriatic skin scale extracts (undetermined 15-OH stereochemistry) and inhibits 5-LO (5-lipoxygenase) with an IC|50|of 26 μM.

Arachidonoyl ethanolamide (AEA) was the first endogenous cannabinoid (CB) to be isolated and characterized as an agonist acting on the same receptors (CB1 and CB2) as THC. Since that time, a number of related endocannabinoids have been isolated,

Arachidonoyl ethanolamide (AEA) was the first endogenous cannabinoid (CB) to be isolated and characterized as an agonist acting on the same receptors (CB1 and CB2) as THC. Since that time, a number of related endocannabinoids have been isolated,

15(S)-HETE-biotin is a major arachidonic acid metabolite produced by the 15-LO (15-lipoxygenase) pathway and is characterized as a potent inhibitor of 5-LO. The mechanism by which 15(S)-HETE acts as a leukotriene inhibitor is not clear. In studies