T2352

AMI-1 is an effective and selective Histone Methyltransferase (HMT) inhibitor (IC50: 3.0/8.8 μM, for yeast Hmt1p, and human PRMT1).

VULM 1457 is a potent ACAT inhibitor. VULM 1457 has remarkable hypolipidaemic activity and improves the overall myocardial ischaemia-reperfusion injury outcomes. VULM1457 significantly reduces production and secretion of adrenomedullin (AM) and down-regulates AM receptors on human hepatoblastic cells.

W-5 hydrochloride (N-(6-Aminohexyl)-1-naphthalenesulfonamide HCl) is a potent calmodulin antagonist.

VUF 8430 dihydrobromide is a potent and selective histamine H4 receptor agonist with a Ki value of 31.6 nM and an EC50 of 50 nM, commonly used in immunology and inflammation research to investigate H4 receptor–mediated signaling, immune cell chemotaxis, cytokine release, and the role of histamine in allergic and inflammatory responses.

W-13 hydrochloride (W-13 HCl) is a calmodulin antagonist.

W-9 hydrochloride is a calmodulin antagonist.

WAY 161503 hydrochloride is a 5-HT2C receptor agonist.

WAY208466 dihydrochloride is a selective and potent 5-HT6 receptor agonist (EC50=7.3 nM) with antidepressant and anxiolytic activity, which can be used for the study of neurological disorders such as depression and anxiety.

WAY-267464 is a non-peptide oxytocin receptor agonist that impairs social cognition in rats by acting as a vasopressin 1A receptor antagonist, making it useful for studying psychiatric disorders.

Protease inhibitor