Piperazin-1-ylpyridazine Derivatives Are a Novel Class of Human dCTP Pyrophosphatase 1 Inhibitors

Sabin Llona‐Minguez, Andreas Höglund, Artin Ghassemian, Matthieu Desroses, José Manuel Calderón‐Montaño, Estefanía Burgos‐Morón, Nicholas C.K. Valerie, Elisée Wiita, Ingrid Almlöf, Tobias Koolmeister,

Journal of Medicinal Chemistry · 2017 · 25 citations · 23 references

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Abstract

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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