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• W2964629852 abstract "Abstract Clinically relevant inhibitors of dihydroorotate dehydrogenase (DHODH), a rate-limiting enzyme in mammalian de novo pyrimidine synthesis, have strong antiviral and anticancer activity in vitro. However, they are ineffective in vivo due to efficient uridine salvage by infected or rapidly dividing cells. The pyrimidine salvage enzyme uridine-cytidine kinase 2 (UCK2), a ∼29 kDa protein that forms a tetramer in its active state, is necessary for uridine salvage. Notwithstanding the pharmacological potential of this target, no medicinally tractable inhibitors of the human enzyme have been reported to date. We therefore established and miniaturized an in vitro assay for UCK2 activity and undertook a high-throughput screen against a ∼ 40,000-compound library to generate drug-like leads. The structures, activities, and modes of inhibition of the most promising hits are described. Notably, our screen yielded non-competitive UCK2 inhibitors which were able to suppress nucleoside salvage in cells both in the presence and absence of DHODH inhibitors." @default.
• W2964629852 created "2019-08-13" @default.
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• W2964629852 date "2019-09-01" @default.
• W2964629852 modified "2023-10-12" @default.
• W2964629852 title "Discovery of small molecule inhibitors of human uridine-cytidine kinase 2 by high-throughput screening" @default.
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• W2964629852 doi "https://doi.org/10.1016/j.bmcl.2019.08.010" @default.
• W2964629852 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6719797" @default.
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