Discovery of novel triazolo[4,3-b]pyridazin-3-yl-quinoline derivatives as PIM inhibitors

• Published in: European journal of medicinal chemistry Vol. 168; pp. 87 - 109
• Main Authors: Martínez-González, Sonia, Rodríguez-Arístegui, Sonsoles, Gómez de la Oliva, Cristina Ana, Hernández, Ana Isabel, González Cantalapiedra, Esther, Varela, Carmen, García, Ana Belén, Rabal, Obdulia, Oyarzabal, Julen, Bischoff, James R., Klett, Javier, Albarrán, María Isabel, Cebriá, Antonio, Ajenjo, Nuria, García-Serelde, Beatriz, Gómez-Casero, Elena, Cuadrado-Urbano, Manuel, Cebrián, David, Blanco-Aparicio, Carmen, Pastor, Joaquín
• Format: Journal Article
• Language: English
• Published: ISSY-LES-MOULINEAUX Elsevier Masson SAS 15.04.2019; Elsevier
• Subjects: Anticancer agents; Antiproliferative activity; Chemical probes; Chemistry, Medicinal; Life Sciences & Biomedicine; pan-PIM inhibitors; Pharmacology & Pharmacy; PIM-1 inhibitors; Science & Technology; Selective PIM-1/PIM-3 inhibitors; Synergistic effects; AML; Synergistic effects; Selective PIM-1/PIM-3 inhibitors; Antiproliferative activity; NSCLC; PIM-1 inhibitors; CRC; MCL; Anticancer agents; Chemical probes; pan-PIM inhibitors; CELLS; APOPTOSIS; PROTOONCOGENE PIM-1; BAD; PANCREATIC-CANCER; PROLIFERATION; SERINE/THREONINE KINASE-ACTIVITY; STRUCTURAL BASIS; GROWTH; EXPRESSION
• ISSN: 0223-5234; 1768-3254
• DOI: 10.1016/j.ejmech.2019.02.022

PIM kinase family (PIM-1, PIM-2 and PIM-3) is an appealing target for the discovery and development of selective inhibitors, useful in various disease conditions in which these proteins are highly expressed, such as cancer. The significant effort put, in the recent years, towards the development of small molecules exhibiting inhibitory activity against this protein family has ended up with several molecules entering clinical trials. As part of our ongoing exploration for potential drug candidates that exhibit affinity towards this protein family, we have generated a novel chemical series of triazolo[4,3-b]pyridazine based tricycles by applying a scaffold hopping strategy over our previously reported potent pan-PIM inhibitor ETP-47453 (compound 2). The structure-activity relationship studies presented herein demonstrate a rather selective PIM-1/PIM-3 biochemical profile for this novel series of tricycles, although pan-PIM and PIM-1 inhibitors have also been identified. Selected examples show significant inhibition of the phosphorylation of BAD protein in a cell-based assay. Moreover, optimized and highly selective compounds, such as 42, did not show significant hERG inhibition at 20 μM concentration, and proved its antiproliferative activity and utility in combination with particular antitumoral agents in several tumor cell lines. [Display omitted] •Novel potent and highly selective tricyclic PIM inhibitors.•Mainly PIM-1/PIM-3 profile; pan-PIM and PIM-1 inhibitors also identified.•Chemical probes to determine PIM isoforms contribution in cancer cell viability.•Synergism of inhibitor 42 in combination with several anticancer agents.•Acceptable in vivo Clearance of selected inhibitors to be used in efficacy studies.