||Atopaxar Hydrobromide is a reversible protease activated receptor (PAR)-1 thrombin receptor antagoni...
||NAD+ is a coenzyme composed of ribosylnicotinamide 5'-diphosphate coupled to adenosine 5'-ph...
||Ambroxol HCl is a potent inhibitor of the neuronal Na+ channels, inhibits TTX-resistant Na+ currents...
||Benidipine HCl is a hydrochloride salt form of benidipine which is a dihydropyridine calcium channel...
||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.