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A series of benzoyl diarylamine/ether derivatives were designed, synthesized, and evaluated for their activity against human immunodeficiency virus (HIV) in MT‐4 cells. Three compounds (3b, 5a, and 6a1) exhibited moderate activities against wild‐type (wt) HIV‐1 with EC50 values ranging from 11 to 56 μm. Among them, compound 5a was the most potent inhibitor with a novel chemical skeleton, affording...
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