| Literature DB >> 28398044 |
Ann L Walker1, Nicolas Ancellin2, Benjamin Beaufils2, Marylise Bergeal3, Margaret Binnie4, Anne Bouillot2, David Clapham3, Alexis Denis2, Carl P Haslam3, Duncan S Holmes1, Jonathan P Hutchinson3, John Liddle1, Andrew McBride4, Olivier Mirguet2, Christopher G Mowat5, Paul Rowland3, Nathalie Tiberghien2, Lionel Trottet2, Iain Uings1, Scott P Webster4, Xiaozhong Zheng6, Damian J Mole6.
Abstract
Recently, we reported a novel role for KMO in the pathogenesis of acute pancreatitis (AP). A number of inhibitors of kynurenine 3-monooxygenase (KMO) have previously been described as potential treatments for neurodegenerative conditions and particularly for Huntington's disease. However, the inhibitors reported to date have insufficient aqueous solubility relative to their cellular potency to be compatible with the intravenous (iv) dosing route required in AP. We have identified and optimized a novel series of high affinity KMO inhibitors with favorable physicochemical properties. The leading example is exquisitely selective, has low clearance in two species, prevents lung and kidney damage in a rat model of acute pancreatitis, and is progressing into preclinical development.Entities:
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Year: 2017 PMID: 28398044 DOI: 10.1021/acs.jmedchem.7b00055
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446