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4. Design, Synthesis and Biological Evaluation: 5-amino-1H-pyrazole-1- carbonyl derivatives as FGFR Inhibitors

8. Convenient one-step synthesis of quinoline-3,4-dicarboxylate derivatives.

9. A new sarkomycin analog from Streptomyces sp. HS-HY-144

14. N-Hydroxy-1,2-disubstituted-1 H-benzimidazol-5-yl acrylamides as novel histone deacetylase inhibitors: Design, synthesis, SAR studies, and in vivo antitumor activity

15. Discovery and Mechanism Study of SIRT1 Activators that Promote the Deacetylation of Fluorophore-Labeled Substrate

16. Discovery of (2E)-3-{2-Butyl-1-[2-(diethylamino)ethyl]-1H-benzimidazol-5-yl}-N-hydroxyacrylamide (SB939), an Orally Active Histone Deacetylase Inhibitor with a Superior Preclinical Profile

19. N-Hydroxy-1,2-disubstituted-1H-benzimidazol-5-yl acrylamides as novel histone deacetylase inhibitors: Design, synthesis, SAR studies, and in vivo antitumor activity

21. SB939: A Potent and Orally Active HDAC Inhibitor for the Treatment of Hematological Malignancies.

22. PLK1 as a potential drug target in cancer therapy

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