Centanafadine is a dual inhibitor of norepinephrine (NE) dopamine (DA) transporter, also inhibits serotonin transporter (IC50s: 6 nM, 38 nM, and 83 nM for humanNE, DA, and serotonin transporter).
AY 254 is a potent PAR2 biased agonist. Selectively activates ERK1 2 signaling (EC50= 2 nM for ERK1 2 phosphorylation versus 80 nM for Ca2+release). Reduces cytoKi ne-induced caspase 3 8 activation, promotes scratch-wound healing, and induces IL-8 secretion, in human colorectal cancer (HT29) cellsin vitro.