Structure-activity relationship for branched oxyquinoline HIF activators: Effect of modifications to phenylacetamide 'tail'
| Autor: | Alexander G. Tonevitsky, Sergey Nikulin, Irina N. Gaisina, D. M. Hushpulian, Andrey A. Poloznikov, Irina G. Gazaryan, Vladimir I. Tishkov, A. A. Zakhariants, N. A. Smirnova |
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| Rok vydání: | 2017 |
| Předmět: |
0301 basic medicine
Stereochemistry Regulator Ring (chemistry) Biochemistry Gene Expression Regulation Enzymologic Hypoxia-Inducible Factor-Proline Dioxygenases Structure-Activity Relationship 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine Acetamides Humans Structure–activity relationship Luciferase Neurons Reporter gene General Medicine Hypoxia-Inducible Factor 1 alpha Subunit Oxyquinoline 030104 developmental biology chemistry Hepatocytes Linker 030217 neurology & neurosurgery Acetamide |
| Zdroj: | Biochimie. 133:74-79 |
| ISSN: | 0300-9084 |
| DOI: | 10.1016/j.biochi.2016.12.004 |
| Popis: | HIF prolyl hydroxylase is a major regulator of HIF stability. Branched tail oxyquinolines have been identified as specific inhibitors of HIF prolyl hydroxylase and recently demonstrated clear benefits in various scenarios of neuronal failure. The structural optimization for branched tail oxyquinolines containing an acetamide bond has been performed in the present study using HIF1 ODD-luc reporter assay. The special attention has been paid to the length of a linker between acetamide group and phenyl ring, as well as substitutions in the phenyl ring in the other branch of the tail. The optimized version of branched tail oxyquinolines is 3-fold more potent than the original one identified before and shows a submicromolar EC 50 in the reporter assay. The compounds have been studied in a “liver-on-a-chip” device to question their hepatotoxicity towards differentiated human HepaRG “hepatocytes”: the absence of hepatotoxicity is observed up to 200 μM concentrations for all studied derivatives of branched tail oxyquinolines. |
| Databáze: | OpenAIRE |
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