Decreasing HepG2 Cytotoxicity by Lowering the Lipophilicity of Benzo[d]oxazolephosphinate Ester Utrophin Modulators
| Autor: | Stephen G. Davies, Angela J. Russell, Enrico Emer, Sarah E. Squire, Maria Chatzopoulou, Francis Xavier Wilson, Lee Moir, Anne-Sophie Casagrande, Kay E. Davies, Jessica A. Rowley, Graham Michael Wynne, Cristina Lecci, Shawn Harriman |
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| Rok vydání: | 2020 |
| Předmět: |
010405 organic chemistry
Chemistry animal diseases Duchenne muscular dystrophy Organic Chemistry Pharmacology musculoskeletal system medicine.disease 01 natural sciences Biochemistry 0104 chemical sciences 010404 medicinal & biomolecular chemistry Drug Discovery Utrophin Lipophilicity medicine Cytotoxicity Therapeutic strategy |
| Zdroj: | ACS Med Chem Lett |
| ISSN: | 1948-5875 |
| DOI: | 10.1021/acsmedchemlett.0c00405 |
| Popis: | [Image: see text] 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 pIC(50) in HepG2 cells, hence leading to a potentially safer toxicological profiles in this series. Compound 21 showed a balanced profile (H2K EC(50): 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. |
| Databáze: | OpenAIRE |
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