| Literature DB >> 33335663 |
Maria Chatzopoulou1, Enrico Emer1, Cristina Lecci2, Jessica A Rowley1, Anne-Sophie Casagrande3, Lee Moir4, Sarah E Squire4, Stephen G Davies1, Shawn Harriman5, Graham M Wynne1, Francis X Wilson5, Kay E Davies4, Angela J Russell1,6.
Abstract
Utrophin modulation is a disease-modifying therapeutic strategy for Duchenne muscular dystrophy that would be applicable to all patient populations. To improve the suboptimal profile of ezutromid, the first-in-class clinical candidate, a second generation of utrophin modulators bearing a phosphinate ester moiety was developed. This modification significantly improved the physicochemical and ADME properties, but one of the main lead molecules was found to have dose-limiting hepatotoxicity. In this work we describe how less lipophilic analogues retained utrophin modulatory activity in a reporter gene assay, upregulated utrophin protein in dystrophic mouse muscle cells, but also had improved physicochemical and ADME properties. Notably, ClogP was found to directly correlate with pIC50 in HepG2 cells, hence leading to a potentially safer toxicological profiles in this series. Compound 21 showed a balanced profile (H2K EC50: 4.17 μM, solubility: 477 μM, mouse hepatocyte T 1/2 > 240 min) and increased utrophin protein 1.6-fold in a Western blot assay.Entities:
Year: 2020 PMID: 33335663 PMCID: PMC7734801 DOI: 10.1021/acsmedchemlett.0c00405
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345