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A series of 4‐(piperazin‐1‐yl)‐7H‐pyrrolo[2,3‐d]pyrimidine derivatives was synthesized and evaluated as Akt inhibitors by optimization of a weak screening lead (1). Typically, compounds 5q and 5t significantly improved the Akt1 inhibitory potency with IC50 values of 18.0 and 21.3 nM, respectively, with desirable antiproliferative effect against the cell lines LNCaP and PC‐3. The inhibitors 5q and...
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