| Literature DB >> 33275878 |
Shaowei Zhang1, Mary E W Collier2, Derren J Heyes1, Flaviano Giorgini2, Nigel S Scrutton3.
Abstract
Kynurenine-3-monooxygenase (KMO) is an important therapeutic target for several brain disorders that has been extensively studied in recent years. Potent inhibitors towards KMO have been developed and tested within different disease models, showing great therapeutic potential, especially in models of neurodegenerative disease. The inhibition of KMO reduces the production of downstream toxic kynurenine pathway metabolites and shifts the flux to the formation of the neuroprotectant kynurenic acid. However, the efficacy of KMO inhibitors in neurodegenerative disease has been limited by their poor brain permeability. Combined with virtual screening and prodrug strategies, a novel brain penetrating KMO inhibitor has been developed which dramatically decreases neurotoxic metabolites. This review highlights the importance of KMO as a drug target in neurological disease and the benefits of brain permeable inhibitors in modulating kynurenine pathway metabolites in the central nervous system.Entities:
Keywords: Brain penetrance; Inhibitor; Kynurenine-3-monooxygenase; Neurodegenerative disease; Prodrug
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Year: 2020 PMID: 33275878 PMCID: PMC8111166 DOI: 10.1016/j.abb.2020.108702
Source DB: PubMed Journal: Arch Biochem Biophys ISSN: 0003-9861 Impact factor: 4.013