Life Science

A more lipid soluble form of (+)-cloprostenol, amenable for certain formulations.

A more lipid soluble form of (+)-cloprostenol, amenable for certain formulations.

A synthetic analog of PGF2&alpha an FP receptor agonist and a potent luteolytic agent in rats and hamsters the optically active, 15(R) enantiomer of cloprostenol responsible for the majority of its biological activity.

A synthetic analog of PGF2&alpha an FP receptor agonist and a potent luteolytic agent in rats and hamsters the optically active, 15(R) enantiomer of cloprostenol responsible for the majority of its biological activity.

A synthetic analog of PGF2&alpha an FP receptor agonist and a potent luteolytic agent in rats and hamsters the optically active, 15(R) enantiomer of cloprostenol responsible for the majority of its biological activity.

An irreversible inhibitor of carnitine palmitoyltransferase 1, a mitochondrial enzyme involved in fatty acid &beta-oxidation (IC50 = 5-20 nM in rat liver) also acts as a direct agonist of PPAR&alpha.

An irreversible inhibitor of carnitine palmitoyltransferase 1, a mitochondrial enzyme involved in fatty acid &beta-oxidation (IC50 = 5-20 nM in rat liver) also acts as a direct agonist of PPAR&alpha.

An irreversible inhibitor of carnitine palmitoyltransferase 1, a mitochondrial enzyme involved in fatty acid &beta-oxidation (IC50 = 5-20 nM in rat liver) also acts as a direct agonist of PPAR&alpha.

An irreversible inhibitor of carnitine palmitoyltransferase 1, a mitochondrial enzyme involved in fatty acid &beta-oxidation (IC50 = 5-20 nM in rat liver) also acts as a direct agonist of PPAR&alpha.

A natural indole alkaloid with demonstrated beneficial effects in cancer, obesity, inflammation, and many other conditions an AhR antagonist (Ki = 28 nM), activator of TRPV1 (EC₅₀ = 45 nM), and inhibitor of signaling through NF-&kappaB.

A natural indole alkaloid with demonstrated beneficial effects in cancer, obesity, inflammation, and many other conditions an AhR antagonist (Ki = 28 nM), activator of TRPV1 (EC₅₀ = 45 nM), and inhibitor of signaling through NF-&kappaB.

A natural indole alkaloid with demonstrated beneficial effects in cancer, obesity, inflammation, and many other conditions an AhR antagonist (Ki = 28 nM), activator of TRPV1 (EC₅₀ = 45 nM), and inhibitor of signaling through NF-&kappaB.