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

Authors :
Llona-Minguez, Sabin
Höglund, Andreas
Ghassemian, Artin
Desroses, Matthieu
Calderon-Montano, Jose Manuel
Moron, Estefania Burgos
Valerie, Nicholas C. K.
Wiita, Elisee
Almlöf, Ingrid
Koolmeister, Tobias
Mateus, André
Cazares-Körner, Cindy
Sanjiv, Kumar
Homan, Evert
Loseva, Olga
Baranczewski, Pawel
Darabi, Masoud
Mehdizadeh, Amir
Fayezi, Shabnam
Jemth, Ann-Sofie
Berglund, Ulrika Warpman
Sigmundsson, Kristmundur
Lundbäck, Thomas
Jensen, Annika Jenmalm
Artursson, Per
Scobie, Martin
Helleday, Thomas
Llona-Minguez, Sabin
Höglund, Andreas
Ghassemian, Artin
Desroses, Matthieu
Calderon-Montano, Jose Manuel
Moron, Estefania Burgos
Valerie, Nicholas C. K.
Wiita, Elisee
Almlöf, Ingrid
Koolmeister, Tobias
Mateus, André
Cazares-Körner, Cindy
Sanjiv, Kumar
Homan, Evert
Loseva, Olga
Baranczewski, Pawel
Darabi, Masoud
Mehdizadeh, Amir
Fayezi, Shabnam
Jemth, Ann-Sofie
Berglund, Ulrika Warpman
Sigmundsson, Kristmundur
Lundbäck, Thomas
Jensen, Annika Jenmalm
Artursson, Per
Scobie, Martin
Helleday, Thomas
Publication Year :
2017

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 sternness. 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.

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1235160516
Document Type :
Electronic Resource
Full Text :
https://doi.org/10.1021.acs.jmedchem.7b00182