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<i>In vivo</i> pharmacokinetic parameters.

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Pharmacokinetic analysis of experimental compounds in rats. Values represent means (% coefficient of variation). Abbreviations: t½: half life; CL: clearance; Vd: volume of distribution; fe: fraction excreted unchanged in urine; Cmax: maximum plasma concentration; Cmin,24 h: minimum plasma concentration within 24 hours after dosing; AUC0-∞: systematic exposure; F: oral bioavailability.

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2014-02-05
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