TY - JOUR
T1 - Progress in the Field of Aldehyde Dehydrogenase Inhibitors: Novel Imidazo[1,2-a]pyridines against the 1A Family
AU - Quattrini, Luca
AU - Gelardi, Edoardo Luigi Maria
AU - Petrarolo, Giovanni
AU - Colombo, Giorgia
AU - FERRARIS, DAVIDE MARIA
AU - Picarazzi, Francesca
AU - RIZZI, Menico
AU - GARAVAGLIA, Silvia
AU - La Motta, Concettina
N1 - Publisher Copyright:
Copyright © 2020 American Chemical Society.
PY - 2020
Y1 - 2020
N2 - Members of the aldehyde dehydrogenase 1A family are commonly acknowledged as hallmarks of cancer stem cells, and their overexpression is significantly associated with poor prognosis in different types of malignancies. Accordingly, treatments targeting these enzymes may represent a successful strategy to fight cancer. In this work we describe a novel series of imidazo[1,2-a]pyridines, designed as aldehyde dehydrogenase inhibitors by means of a structure-based optimization of a previously developed lead. The novel compounds were evaluated in vitro for their activity and selectivity against the three isoforms of the ALDH1A family and investigated through crystallization and modeling studies for their ability to interact with the catalytic site of the 1A3 isoform. Compound 3f emerged as the first in class submicromolar competitive inhibitor of the target enzyme.
AB - Members of the aldehyde dehydrogenase 1A family are commonly acknowledged as hallmarks of cancer stem cells, and their overexpression is significantly associated with poor prognosis in different types of malignancies. Accordingly, treatments targeting these enzymes may represent a successful strategy to fight cancer. In this work we describe a novel series of imidazo[1,2-a]pyridines, designed as aldehyde dehydrogenase inhibitors by means of a structure-based optimization of a previously developed lead. The novel compounds were evaluated in vitro for their activity and selectivity against the three isoforms of the ALDH1A family and investigated through crystallization and modeling studies for their ability to interact with the catalytic site of the 1A3 isoform. Compound 3f emerged as the first in class submicromolar competitive inhibitor of the target enzyme.
UR - https://iris.uniupo.it/handle/11579/112728
U2 - 10.1021/acsmedchemlett.9b00686
DO - 10.1021/acsmedchemlett.9b00686
M3 - Article
SN - 1948-5875
JO - ACS Medicinal Chemistry Letters
JF - ACS Medicinal Chemistry Letters
ER -