| Literature DB >> 28002958 |
John S Debenham1, Christina Madsen-Duggan1, Matthew J Clements1, Thomas F Walsh1, Jeffrey T Kuethe1, Mikhail Reibarkh1, Scott P Salowe1, Lisa M Sonatore1, Richard Hajdu1, James A Milligan1, Denise M Visco1, Dan Zhou1, Russell B Lingham1, Dominique Stickens1, Julie A DeMartino1, Xinchun Tong1, Michael Wolff1, Jianmei Pang1, Randy R Miller1, Edward C Sherer1, Jeffrey J Hale1.
Abstract
The discovery of novel 4-hydroxy-2-(heterocyclic)pyrimidine-5-carboxamide inhibitors of hypoxia-inducible factor (HIF) prolyl hydroxylases (PHD) is described. These are potent, selective, orally bioavailable across several species, and active in stimulating erythropoiesis. Mouse and rat studies showed hematological changes with elevations of plasma EPO and circulating reticulocytes following single oral dose administration, while 4-week q.d. po administration in rat elevated hemoglobin levels. A major focus of the optimization process was to decrease the long half-life observed in higher species with early compounds. These efforts led to the identification of 28 (MK-8617), which has advanced to human clinical trials for anemia.Entities:
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Year: 2016 PMID: 28002958 DOI: 10.1021/acs.jmedchem.6b01242
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446