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Journal of Medicinal Chemistry|January 24, 2018
Design, Synthesis, and Preclinical Evaluation of Fused Pyrimidine-Based Hydroxamates for the Treatment of Hepatocellular CarcinomaDizhong Chen, Chang Kai Soh, Wei Huang Goh, et al.Bioorganic Chemistry|March 16, 2020
Synthesis and biological evaluation of 6-phenylpurine linked hydroxamates as novel histone deacetylase inhibitorsDizhong Chen, Chang Kai Soh, Wei Huang Goh, et al.Bioorganic & Medicinal Chemistry Letters|November 29, 2011
Structure-based design of PDK1 inhibitorsAnders Poulsen, Stéphanie Blanchard, Chang Kai Soh, et al.Bioorganic & Medicinal Chemistry Letters|December 27, 2011
Structure-based optimization of morpholino-triazines as PI3K and mTOR inhibitorsAnders Poulsen, Meredith Williams, Harish Mysore Nagaraj, et al.Journal of Chemical Information and Modeling|October 16, 2014
Structure and ligand-based design of mTOR and PI3-kinase inhibitors leading to the clinical candidates VS-5584 (SB2343) and SB2602Anders Poulsen, Harish Nagaraj, Angeline Lee, et al.Bioorganic & Medicinal Chemistry Letters|March 23, 2012
2-anilino-4-aryl-8H-purine derivatives as inhibitors of PDK1Stéphanie Blanchard, Chang Kai Soh, Chai Ping Lee, et al.Pageof 1