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This unique binding method underpins its functional selectivity, as interactions with TM6/seven are crucial for β-arrestin activation .
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Q. How can this compound's pharmacological profile be optimized to scale back Unintended effects though keeping analgesia?
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Standardize Agonist Exposure Times : this compound’s sluggish dissociation kinetics require extended observation durations to capture whole β-arrestin recruitment .
This substance is often a research substance and is intended for analyze in specially Geared up laboratories.
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