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[Biochemical screening and subsequent structure-based hit optimization yielded inhibitors of the KRAS-PDE? interaction that selectively bind to the prenyl-binding pocket of PDE? with nanomolar affinity, inhibit oncogenic RAS signalling and suppress in vitro and in vivo proliferation of human pancreatic ductal adenocarcinoma cells that are dependent on oncogenic KRAS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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