This series-level difference was highly significant with D103A, S198A, S202A mutations having more impact on catechol agonism, and S188I mutations showing more impact on non-catechol agonism when comparing Δpotency for all compounds in a class.
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Impaired β-arrestin recruitment and reduced desensitization by non-catechol agonists of the D1 dopamine receptor.
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