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Synthesis and structure-activity relationship of 6-arylureido-3-pyrrol-2-ylmethylideneindolin-2-one derivatives as potent receptor tyrosine kinase inhibitors.
Khanwelkar RR, Chen GS, Wang HC, Yu CW, Huang CH, Lee O, Chen CH, Hwang CS, Ko CH, Chou NT, Lin MW, Wang LM, Chen YC, Hseu TH, Chang CN, Hsu HC, Lin HC, Shih YC, Chou SH, Tseng HW, Liu CP, Tu CM, Hu TL, Tsai YJ, Chern JW. Khanwelkar RR, et al. Among authors: yu cw. Bioorg Med Chem. 2010 Jul 1;18(13):4674-86. doi: 10.1016/j.bmc.2010.05.021. Epub 2010 May 12. Bioorg Med Chem. 2010. PMID: 20570526
A highly HDAC6-selective inhibitor acts as a fluorescent probe.
Ho YH, Wang KJ, Hung PY, Cheng YS, Liu JR, Fung ST, Liang PH, Chern JW, Yu CW. Ho YH, et al. Among authors: yu cw. Org Biomol Chem. 2018 Oct 31;16(42):7820-7832. doi: 10.1039/c8ob00966j. Org Biomol Chem. 2018. PMID: 30168823
Discovery of HDAC6, HDAC8, and 6/8 Inhibitors and Development of Cell-Based Drug Screening Models for the Treatment of TGF-β-Induced Idiopathic Pulmonary Fibrosis.
Yu WC, Yeh TY, Ye CH, Chong PCT, Ho YH, So DK, Yap KY, Peng GR, Shao CH, Jagtap AD, Chern JW, Lin CS, Lin SP, Lin SL, Yu SH, Yu CW. Yu WC, et al. Among authors: yu cw, yu sh. J Med Chem. 2023 Aug 10;66(15):10528-10557. doi: 10.1021/acs.jmedchem.3c00644. Epub 2023 Jul 18. J Med Chem. 2023. PMID: 37463500
465 results