Journal of Medicinal Chemistry · 2017 · 25 citations · 23 references
PharmacyMedicinal ChemistryOncologyDrug DiscoveryEnzymologyMolecular OncologyEnzyme InhibitionHit-to-lead OptimizationLead Compound DesignLead DiscoveryCytidine Nucleotide MetabolismEnzyme Inhibitor DiscoveryEnzymesLead Enzyme DiscoveryProtease InhibitorsProtease SelectivityPyrimidine AnaloguesSelectivity
The dCTP pyrophosphatase 1 (dCTPase) is a nucleotide pool "housekeeping" enzyme responsible for the catabolism of canonical and noncanonical nucleoside triphosphates (dNTPs) and has been associated with cancer progression and cancer cell stemness. We have identified a series of piperazin-1-ylpyridazines as a new class of potent dCTPase inhibitors. Lead compounds increase dCTPase thermal and protease stability, display outstanding selectivity over related enzymes and synergize with a cytidine analogue against leukemic cells. This new class of dCTPase inhibitors lays the first stone toward the development of drug-like probes for the dCTPase enzyme.
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Monitoring Drug Target Engagement in Cells and Tissues Using the Cellular Thermal Shift Assay
Daniel Martinez Molina, Rozbeh Jafari, Marina Ignatushchenko et al. · Science · 2013 · 2.2K citations
Medicine, Oncology, Pharmacology +17
Target identification using drug affinity responsive target stability (DARTS)
Brett Lomenick, Rui Hao, Nao Jonai et al. · Proceedings of the National Academy of Sciences · 2009 · 1.1K citations · Full text