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CTEP is a **research drug** developed by Hoffmann-La Roche that acts as a **selective allosteric antagonist** of the **metabotropic glutamate receptor subtype 5 (mGluR5)**. It binds with nanomolar affinity and shows over 1000-fold selectivity over other receptor targets tested. In animal studies, CTEP demonstrates high oral bioavailability and a long duration of action (lasting up to 18 hours after single dose), making it an improvement over earlier mGluR5 antagonists such as MPEP and fenobam. Its principal use is as a research tool in central nervous system studies, particularly for disorders related to glutamatergic signaling[1].
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