Ticlopidine Hydrochloride AS inhibitor and orally bioavailable inhibitor of

and orally bioavailable inhibitor of histone deacetylase 6 (HDAC6)

and competitive antagonist of BET bromodomains to hijack the Cereblon E3 ubiquitin ligase complex

Bephenium is an anthelmintic agent formerly used in the treatment of hookworm infections and ascariasis

Effects of thiocyanate and AMPA receptor ligands on (S)-5-fluorowillardiine

Formula: C41H71N3O8

Ticlopidine Hydrochloride AS inhibitor and orally bioavailable inhibitor ofTiclopidine is an antiplatelet drug in the thienopyridine family which is an adenosine diphosphate (ADP) receptor inhibitor. Research initially showed that it was useful for preventing strokes and coronary stent occlusions. However, because of its rare but serious side effects of neutropenia and thrombotic thrombocytopenic purpura it was primarily used in patients in whom aspirin was not tolerated, or in whom dual antiplatelet therapy was desirable.