| Literature DB >> 28508636 |
Sabin Llona-Minguez1, Andreas Höglund1, Artin Ghassemian1, Matthieu Desroses1, José Manuel Calderón-Montaño1, Estefanía Burgos Morón1, Nicholas C K Valerie1, Elisee Wiita1, Ingrid Almlöf1, Tobias Koolmeister1, André Mateus2, Cindy Cazares-Körner1, Kumar Sanjiv1, Evert Homan1, Olga Loseva1, Pawel Baranczewski2, Masoud Darabi3, Amir Mehdizadeh3, Shabnam Fayezi4, Ann-Sofie Jemth1, Ulrika Warpman Berglund1, Kristmundur Sigmundsson1,5, Thomas Lundbäck1,5, Annika Jenmalm Jensen1,5, Per Artursson2, Martin Scobie1, Thomas Helleday1.
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.Entities:
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Year: 2017 PMID: 28508636 DOI: 10.1021/acs.jmedchem.7b00182
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446