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Peking Univ. FGFR4 compound 30: sourced facts only. name: "Representative compounds 24 and 30 exhibited potent FGFR4 inhibition and high selectivity among kinases." [PMID:35549181]; target: "Representative compounds 24 and 30 exhibited potent FGFR4 inhibition and high selectivity among kinases." [PMID:35549181]; developer: "State Key Laboratory of Chemical Oncogenomics, Key Laboratory of Chemical Genomics, School of Chemical Biology and Biotechnology, Shenzhen Graduate School, Peking University, Shenzhen 518055, China." [PMID:35549181]; stage: "Moreover, compound 30 exhibited significant in vivo antitumor activity in a mouse HuH-7 xenograft model." [PMID:35549181]
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