Discovery and Optimization of a Series of 3-(3-Phenyl-3H-imidazo[4,5-b]pyridin-2-yl)pyridin-2-amines: Orally Bioavailable, Selective, and Potent ATP-Independent Akt Inhibitors
| Autor: | Mark A. Ashwell, Jean-Marc Lapierre, Christopher Brassard, Karen Bresciano, Cathy Bull, Susan Cornell-Kennon, Sudharshan Eathiraj, Dennis S. France, Terence Hall, Jason Hill, Eoin Kelleher, Sampada Khanapurkar, Darin Kizer, Steffi Koerner, Jeff Link, Yanbin Liu, Sapna Makhija, Magdi Moussa, Nivedita Namdev, Khanh Nguyen, Robert Nicewonger, Rocio Palma, Jeff Szwaya, Manish Tandon, Uma Uppalapati, David Vensel, Laurie P. Volak, Erika Volckova, Neil Westlund, Hui Wu, Rui-Yang Yang, Thomas C. K. Chan |
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| Rok vydání: | 2012 |
| Předmět: |
Models
Molecular Protein Conformation Pyridines Administration Oral Biological Availability AKT1 Antineoplastic Agents Plasma protein binding Pharmacology Crystallography X-Ray Mice Structure-Activity Relationship Adenosine Triphosphate In vivo Catalytic Domain Cell Line Tumor Drug Discovery Animals Humans Structure–activity relationship Phosphorylation Protein kinase B Adaptor Proteins Signal Transducing Cell Proliferation Effector Chemistry Imidazoles Ribosomal Protein S6 Kinases 70-kDa Small molecule Biochemistry Microsomes Liver Molecular Medicine Proto-Oncogene Proteins c-akt Protein Binding |
| Zdroj: | Journal of Medicinal Chemistry. 55:5291-5310 |
| ISSN: | 1520-4804 0022-2623 |
| Popis: | This paper describes the implementation of a biochemical and biophysical screening strategy to identify and optimize small molecule Akt1 inhibitors that act through a mechanism distinct from that observed for kinase domain ATP-competitive inhibitors. With the aid of an unphosphorylated Akt1 cocrystal structure of 12j solved at 2.25 Å, it was possible to confirm that as a consequence of binding these novel inhibitors, the ATP binding cleft contained a number of hydrophobic residues that occlude ATP binding as expected. These Akt inhibitors potently inhibit intracellular Akt activation and its downstream target (PRAS40) in vitro. In vivo pharmacodynamic and pharmacokinetic studies with two examples, 12e and 12j, showed the series to be similarly effective at inhibiting the activation of Akt and an additional downstream effector (p70S6) following oral dosing in mice. |
| Databáze: | OpenAIRE |
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