Pioglitazone hydrochloride

(+)-Cloprostenol (sodium salt) is a more water soluble, crystalline form of (+)-cloprostenol. (+)-Cloprostenol is a synthetic analog of prostaglandin F2α (PGF2α). It is an FP receptor agonist and a potent luteolytic agent in rats and hamsters.

(+)-Cloprostenol (sodium salt) is a more water soluble, crystalline form of (+)-cloprostenol. (+)-Cloprostenol is a synthetic analog of prostaglandin F2α (PGF2α). It is an FP receptor agonist and a potent luteolytic agent in rats and hamsters.

Functionalized BET bromodomain inhibitor: 'click' target ligand for PROTACs.

Functionalized BET bromodomain inhibitor: 'click' target ligand for PROTACs.

Functionalized BET bromodomain inhibitor: 'click' target ligand for PROTACs.

Application Chloro-APB hydrobromide has been used to pharmacologically stimulate D1 dopamine receptors and study its influence on locomotor response in fat mass and obesity-associated protein (FTO) deficient dopamine D1 receptor-expressing medium

Application Chloro-APB hydrobromide has been used to pharmacologically stimulate D1 dopamine receptors and study its influence on locomotor response in fat mass and obesity-associated protein (FTO) deficient dopamine D1 receptor-expressing medium

Cloprostenol is a synthetic analogue of prostaglandin F2&#945 (PGF). Cloprostenol contributes to the induction of estrus in animals and has uterotonic activity.

Cloprostenol is a synthetic analogue of prostaglandin F2&#945 (PGF). Cloprostenol contributes to the induction of estrus in animals and has uterotonic activity.

Biochem/physiol Actions (2S,6S)-Hydroxynorketamine hydrochlorideKetamine is a metabolite associated with increased locomotor activity and motor incoordination. It has been found that the NMDAR antagonist (R,S)-ketamine must be metabolized to

(BTO) OVARIAN CANCER Controls /Pk (25)

(R)-BAY-899 is the R-enantiomer of BAY-899. BAY-899 is an orally active and selective luteinizing hormone receptor (LH-R) antagonist with IC50s of 185 nM and 46nM for hLH (human LH) and rLH (rat LH), respectively.Biological Activity:(R)-BAY-899 is