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Discovery of the First Potent and Selective Inhibitors of Human dCTP Pyrophosphatase 1

Authors :
Llona-Minguez, Sabin
Höglund, Andreas
Jacques, Sylvain A.
Johanson, Lars
Calderon-Montano, Jose Manuel
Claesson, Magnus
Loseva, Olga
Valerie, Nicholas C. K.
Lundback, Thomas
Piedrafita, Javier
Maga, Giovanni
Crespan, Emmanuele
Meijer, Laurent
Moron, Estefania Burgos
Baranczewski, Pawel
Hagbjörk, Ann-Louise
Svensson, Richard
Wiita, Elisee
Almlof, Ingrid
Visnes, Torkild
Jeppsson, Fredrik
Sigmundsson, Kristmundur
Jensen, Annika Jenmalm
Artursson, Per
Jemth, Ann-Sofie
Stenmark, Pal
Berglund, Ulrika Warpman
Scobie, Martin
Helleday, Thomas
Llona-Minguez, Sabin
Höglund, Andreas
Jacques, Sylvain A.
Johanson, Lars
Calderon-Montano, Jose Manuel
Claesson, Magnus
Loseva, Olga
Valerie, Nicholas C. K.
Lundback, Thomas
Piedrafita, Javier
Maga, Giovanni
Crespan, Emmanuele
Meijer, Laurent
Moron, Estefania Burgos
Baranczewski, Pawel
Hagbjörk, Ann-Louise
Svensson, Richard
Wiita, Elisee
Almlof, Ingrid
Visnes, Torkild
Jeppsson, Fredrik
Sigmundsson, Kristmundur
Jensen, Annika Jenmalm
Artursson, Per
Jemth, Ann-Sofie
Stenmark, Pal
Berglund, Ulrika Warpman
Scobie, Martin
Helleday, Thomas
Publication Year :
2016

Abstract

The dCTPase pyrophosphatase 1 (dCTPase) regulates the intracellular nucleotide pool through hydrolytic degradation of canonical and noncanonical nucleotide triphosphates (dNTPs). dCTPase is highly expressed in multiple carcinomas and is associated with cancer cell sternness. Here we report on the development of the first potent and selective dCTPase inhibitors that enhance the cytotoxic effect of cytidine analogues in leukemia cells. Boronate 30 displays a promising in vitro ADME profile, including plasma and mouse microsomal half-lives, aqueous solubility, cell permeability and CYP inhibition, deeming it a suitable compound for in vivo studies.

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1235134091
Document Type :
Electronic Resource
Full Text :
https://doi.org/10.1021.acs.jmedchem.5b01741