||TRAM-34 is a selective and potent inhibitor of the intermediate-conductance Ca2+-activated K+ channe...
||R406 is a potent Syk inhibitor with IC50 of 41 nM, strongly inhibits Syk but not Lyn, 5-fold less po...
||GW501516 is a potent and highly selective PPARβ/δ agonist, with EC50 of 1 nM, with 1000-fold selecti...
||Verdinexor (KPT-335) is an orally bioavailable, selective XPO1/CRM1 inhibitor.
||Darapladib (SB-480848) is a reversible lipoprotein-associated phospholipase A2 (Lp-PLA2) inhibitor w...
||KPT-276 is an orally bioavailable selective CRM1 inhibitor.
||Brefeldin A is a lactone antibiotic and ATPase inhibitor for protein transport with IC50 of 0.2 μM i...
||Blebbistatin is a selective inhibitor of myosin II ATPase activity with IC50 of 0.5 - 5 μM