Discovery of the First Vitamin K Analogue as a Potential Treatment of Pharmacoresistant Seizures

Despite the availability of more than 25 antiseizure drugs on the market, approximately 30% of patients with epilepsy still suffer from seizures. Thus, the epilepsy therapy market has a great need for a breakthrough drug that will aid pharmacoresistant patients. In our previous study, we discovered...

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Veröffentlicht in:Journal of medicinal chemistry 2020-06, Vol.63 (11), p.5865-5878
Hauptverfasser: Li, Xiaoyang, Himes, Richard A, Prosser, Lyndsey C, Christie, Charleston F, Watt, Emma, Edwards, Sharon F, Metcalf, Cameron S, West, Peter J, Wilcox, Karen S, Chan, Sherine S L, Chou, C James
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Sprache:eng
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Zusammenfassung:Despite the availability of more than 25 antiseizure drugs on the market, approximately 30% of patients with epilepsy still suffer from seizures. Thus, the epilepsy therapy market has a great need for a breakthrough drug that will aid pharmacoresistant patients. In our previous study, we discovered a vitamin K analogue, , which displayed modest antiseizure activity in zebrafish and mouse seizure models. However, there are limitations to this compound due to its pharmacokinetic profile. In this study, we develop a new series of vitamin K analogues by modifying the structure of . Among these, compound shows full protection in a rodent pharmacoresistant seizure model with limited rotarod motor toxicity and favorable pharmacokinetic properties. Furthermore, the brain/plasma concentration ratio of indicates its excellent permeability into the brain. The resulting data shows that can be further developed as a potential antiseizure drug in the clinic.
ISSN:0022-2623
1520-4804
DOI:10.1021/acs.jmedchem.0c00168