A novel series of benzenesulfonamide derivatives that selectively act on the AT receptor have been designed and synthesized. The binding affinity and functional activity were evaluated by radio-ligand binding analysis and cell neurite outgrowth assay, respectively. The compounds , , , , , and exhibited moderate selectivity and affinity for the AT receptor. Among them, exhibited agonist activity and displayed similar selectivity to the AT receptor with . Molecular docking was carried out to analyze the binding mode and binding site between the compound and the AT receptor to provide a reference for further development.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9458978PMC
http://dx.doi.org/10.3389/fchem.2022.984717DOI Listing

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