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Description

Selective D4 receptor antagonist with excellent brain penetration. Displays an affinity (Ki) of 0.4 nM for human D4 receptors with >1000-fold binding selectivity over D2 and D3 receptors. Does not block agonist-induced activation of GIRK currents. It is used frequently in retinal and CNS studies of D4 modulation.

Structure formula

L-745,870 Trihydrochloride

Contents

Miscellaneous

Certificate of Analysis (specimen)

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Product data sheet

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