Facilitates agonist induced elevation of cytosolic calcium at low concentrations (10µM). Antagonizes calmodulin at higher concentrations. Antipsychotic and sedative dopamine antagonist. Potent and irreversible inhibitor of cAMP-gated cationic channels. Inhibits DNA repair. Cell permeable. Potent neurotoxin.
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Regulatory Status |
RUO – Research Use Only |
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