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Published in Journal of medicinal chemistry (11.02.2021)
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Design and synthesis of pyrrole–5-(2,6-dichlorobenzyl)sulfonylindolin-2-ones with C-3′ side chains as potent Met kinase inhibitors
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Abstract C046: A Smo inhibitor DCBCO1303 with potent Hedgehog signaling pathway antagonist activity is highly active in animal tumor model of medulloblastoma and cholangiocarcinoma
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Published in Molecular cancer therapeutics (01.12.2019)
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Copper(I)-Catalyzed Nitrile-Addition/N-Arylation Ring-Closure Cascade: Synthesis of 5,11-Dihydro‑6H‑indolo[3,2‑c]quinolin-6-ones as Potent Topoisomerase‑I Inhibitors
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Design and synthesis of pyrrole-5-(2,6-dichlorobenzyl)sulfonylindolin-2-ones with C-3′ side chains as potent Met kinase inhibitorsElectronic supplementary information (ESI) available: Ligplot diagrams of the ATP binding site of Met complexed with compounds 2 and 20, and the kinase profiling data of 20. See DOI: 10.1039/c4ra08720h
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Synthesis and structure-activity relationship of 3-0-acylated (-)-epigallocatechins as 5α-reductase inhibitors
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Published in European journal of medicinal chemistry (2010)
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Published in European journal of medicinal chemistry (2010)
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