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Bivalent and induced-fit binding drugs may display quite distinct in vivo target occupancy profiles even when they have the same potency. This difference stems from the different impact of their microscopic rate constants, not only on their dissociation rate but also on their susceptibility to experience rebinding.

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This page is a summary of: Distinct in vivo target occupancy by bivalent‐ and induced‐fit‐like binding drugs, British Journal of Pharmacology, October 2017, Wiley,
DOI: 10.1111/bph.13989.
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