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In vitro signaling profiles and propensities for receptor desensitization of two clinically studied FPR2 agonists, namely, BMS-986235 and ACT-389949, were evaluated
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Linearity has been shown over the reduced concentration range 0.030.5 mg/L whereas a multiplicative model (lnln transformation) had to be used to describe the full range of concentrations 0.0320 mg/L
