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Journal of Medicinal Chemistry|November 8, 2013
Exploration of a series of 5-arylidene-2-thioxoimidazolidin-4-ones as inhibitors of the cytolytic protein perforinJulie A Spicer, Gersande Lena, Dani M Lyons, et al.
European Journal of Medicinal Chemistry|May 7, 2013
Synthesis and biological evaluation of novel phosphatidylinositol 3-kinase inhibitors: Solubilized 4-substituted benzimidazole analogs of 2-(difluoromethyl)-1-[4,6-di(4-morpholinyl)-1,3,5-triazin-2-yl]-1H-benzimidazole (ZSTK474)Gordon W Rewcastle, Swarna A Gamage, Jack U Flanagan, et al.
Bioorganic & Medicinal Chemistry Letters|December 8, 2016
Novel pyrazolo[1,5-a]pyridines with improved aqueous solubility as p110α-selective PI3 kinase inhibitorsJackie D Kendall, Anna C Giddens, Kit Yee Tsang, et al.
Inorganic Chemistry|February 20, 2020
Potent Inhibition of Thioredoxin Reductase by the Rh Derivatives of Anticancer M(arene/Cp*)(NHC)Cl2 ComplexesDianna Truong, Matthew P Sullivan, Kelvin K H Tong, et al.
Biochemical Pharmacology|January 18, 2014
A novel fluorometric assay for aldo-keto reductase 1C3 predicts metabolic activation of the nitrogen mustard prodrug PR-104A in human leukaemia cellsStephen M F Jamieson, Yongchuan Gu, Donya Moradi Manesh, et al.
Bioorganic & Medicinal Chemistry|December 20, 2011
Discovery of pyrazolo[1,5-a]pyridines as p110α-selective PI3 kinase inhibitorsJackie D Kendall, Patrick D O'Connor, Andrew J Marshall, et al.
Bioorganic & Medicinal Chemistry|December 20, 2011
Novel pyrazolo[1,5-a]pyridines as p110α-selective PI3 kinase inhibitors: Exploring the benzenesulfonohydrazide SARJackie D Kendall, Anna C Giddens, Kit Yee Tsang, et al.
European Journal of Medicinal Chemistry|September 16, 2023
Fragment-based and structure-guided discovery of perforin inhibitorsJiney Jose, Ruby H P Law, Eleanor W W Leung, et al.
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