CZC-25146 is a potent and selective LRRK2 inhibitor. CZC-25146 prevents mutant LRRK2-induced injury of cultured rodent and human neurons with mid-nanomolar potency.
More Information Supplier PageCZC-25146 is a potent and selective LRRK2 inhibitor. CZC-25146 prevents mutant LRRK2-induced injury of cultured rodent and human neurons with mid-nanomolar potency.
More Information Supplier PageA-484954 is a potent, selective inhibitor of eukaryotic longation factor-2 kinase (eEF2K).
More Information Supplier PageA-484954 is a potent, selective inhibitor of eukaryotic longation factor-2 kinase (eEF2K).
More Information Supplier PageA-484954 is a potent, selective inhibitor of eukaryotic longation factor-2 kinase (eEF2K).
More Information Supplier PageLY364947 is a diheteroaryl-substituted pyrazole compound used as a selective, ATP-competitive inhibitor of TGF-??RI (TGF-?? Receptor I kinase).
More Information Supplier PageLY364947 is a diheteroaryl-substituted pyrazole compound used as a selective, ATP-competitive inhibitor of TGF-??RI (TGF-?? Receptor I kinase).
More Information Supplier PageLY364947 is a diheteroaryl-substituted pyrazole compound used as a selective, ATP-competitive inhibitor of TGF-??RI (TGF-?? Receptor I kinase).
More Information Supplier Page(-)-MK 801 maleate acts as a potent, selective, and non-competitive NMDA receptor antagonist. It acts by binding to a site located within the NMDA associated ion channel.
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