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Biochimica Et Biophysica Acta. General Subjects|February 6, 2017
Identification of TG100-115 as a new and potent TRPM7 kinase inhibitor, which suppresses breast cancer cell migration and invasionChiman Song, Yeonju Bae, JinJoo Jun, et al.Journal of the American Chemical Society|February 16, 2006
Discovery of EGFR selective 4,6-disubstituted pyrimidines from a combinatorial kinase-directed heterocycle libraryQiong Zhang, Yi Liu, Feng Gao, et al.Chemical Biology & Drug Design|April 18, 2023
Identification of novel class inhibitors of NSD3 methyltransferase showing a unique, bivalent binding mode in the SET domainSumin Kim, Injeoung Hwang, Suhn Hyung Kim, et al.Chemical Biology & Drug Design|November 8, 2014
A Discovery Strategy for Selective Inhibitors of c-Src in Complex with the Focal Adhesion Kinase SH3/SH2-binding RegionJamie A Moroco, Matthew P Baumgartner, Heather L Rust, et al.Chemistry & Biology|June 11, 2010
A small-molecule inducer of the antioxidant response elementWooyoung Hur, Zheng Sun, Tao Jiang, et al.ACS Chemical Biology|April 13, 2012
Selective ATP-competitive inhibitors of TOR suppress rapamycin-insensitive function of TORC2 in Saccharomyces cerevisiaeQingsong Liu, Tao Ren, Tara Fresques, et al.Chemistry & Biology|May 5, 2004
Synthesis and target identification of hymenialdisine analogsYongqin Wan, Wooyoung Hur, Charles Y Cho, et al.Journal of Medicinal Chemistry|August 29, 2018
First SAR Study for Overriding NRAS Mutant Driven Acute Myeloid LeukemiaHanna Cho, Injae Shin, Eunhye Ju, et al.European Journal of Medicinal Chemistry|December 7, 2023
Identification of a novel potent CDK inhibitor degrading cyclinK with a superb activity to reverse trastuzumab-resistance in HER2-positive breast cancer in vivoRatnakar Reddy Kuchukulla, Injeoung Hwang, Suhn Hyung Kim, et al.Bioorganic & Medicinal Chemistry Letters|October 21, 2018
Design, synthesis, and biological evaluation of novel aminopyrimidinylisoindolines as AXL kinase inhibitorsMin Jung Choi, Eun Joo Roh, Wooyoung Hur, et al.Pageof 5