Burger, Matthew, Nishiguchi, Gisele, Han, Wooseok, Lan, Jiong, Simmons, Bob, Atallah, Gordana, Ding, Yu, Tamez Jr., Victoriano, zhang, yanchen, mathur, michelle, muller, kristine, Bellamacina, Cornelia, Lindvall, Mika, Zang, Richard, Huh, Kay, Feucht, Paul, Zavorotinskaya, Tatiana, Dai, Yumin, Basham, Steve, Chan, Julie, Ginn, Elaine, Aycinena, Alex, Holash, Jocelyn, Castillo, Joseph, Langowski, John, Wang, Yingyun, Chen, Min, Lambert, Amy, Fritsch, Christine, Kauffmann, Audrey, Pfister-Wagner, Estelle, Vanasse, K. Gary and Garcia, Pablo (2015) Identification of N-(4-((1R,3S,5S)-3-amino-5-methylcyclohexyl)pyridin-3-yl)-6-(2,6-difluorophenyl)-5-fluoropicolinamide (PIM447), a Potent and Selective Proviral Insertion Site of Moloney Murine Leukemia (PIM) 1,2 and 3 Kinase Inhibitor in Clinical Trials for Hematological Malignancies. Journal of Medicinal Chemistry.

Abstract

Pan Proviral Insertion Site of Moloney Murine Leukemia (PIM) 1, 2 and 3 kinase inhibitors have recently begun to be tested in humans to assess whether pan PIM kinase inhibition may provide benefit to cancer patients. Herein, the synthesis, in vitro activity, in vivo activity in an acute myeloid leukemia xenograft model and pre-clinical profile of the potent and selective pan PIM kinase inhibitor 8 (PIM447) are described. Starting from the reported aminopiperidyl pan PIM kinase inhibitor 1, a strategy to improve the microsomal stability was pursued resulting in the identification of potent aminocyclohexyl pan PIM inhibitors with high metabolic stability. From this aminocyclohexyl series, 8 entered the clinic in 2012 in multiple myeloma patients and is currently in several phase 1 trials of cancer patients with hematological malignancies.

Item Type:	Article
Date Deposited:	18 Dec 2015 00:45
Last Modified:	18 Dec 2015 00:45
URI:	https://oak.novartis.com/id/eprint/26675