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Efficient Synthesis and Biological Evaluation of 1,4-Disubstituted 3-Cyanopyridin-2(1H)-ones as Selective Inhibitors of the Post-Acid Activity of Mammalian 20S Proteasomes

Crossref DOI link: https://doi.org/10.1134/S107042802460373X

Published Online: 2025-05-07

Published Print: 2025-03

Update policy: https://doi.org/10.1007/springer_crossmark_policy

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