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Description: BAY-1797 is a highly potent, orally bioavailable, and specific P2X4 antagonist with an IC50 of 211 nM against human P2X4. BAY-1797 displays no or very weak activity on the other P2X ion channels. BAY-1797 shows anti-nociceptive and anti-inflammatory effects. Theanti-inflammatory and anti-nociceptive effects of BAY-1797 weredemonstrated in a mouse complete Freund's adjuvant (CFA) inflammatorypain model.
References: Discoveryand Characterization of the Potent and Selective P2X4 InhibitorN-4-(3-Chlorophenoxy)-3-sulfamoylphenyl-2-phenylacetamide (BAY-1797)and Structure-Guided Amelioration of Its CYP3A4 Induction Profile. J MedChem. 2019 Dec 26; 62(24):11194-11217.
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