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This poster discusses the development of EPSA, reviews its applications as a predictive tool for passive membrane permeability, and highlights its significance in designing drugs with high oral bioavailability. We further optimized the chromatographic conditions (reducing single-needle detection time to 6.5 minutes) to measure EPSA, present data for a range of bRo5 and Ro5 compounds, and offer alternative high-throughput and high-quality detection methods for drug screening in the drug discovery stage.
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