Synthesis and the hepatoprotective activity of dibenzocyclooctadiene lignan derivatives |
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Affiliation: | 1. Departamento de Teoria de la Senãl y Comunicaciones. Universidad Carlos III de Madrid Avenida de la Universidad, 30. 28911 Leganes (Madrid), Spain;2. AGH University of Science and Technology, Faculty of Computer Science, Electronics and Telecommunications al. Mickiewicza 30, 30-059 Krakow, Poland |
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Abstract: | The halogenated and oxidized derivatives (1a–1e, 1a′–1c′, 2a–2d, 2a′–2b′, 3a–3e, 3′ and 3a′–3b′) of schizandrin (1), schizandrin B (2) and schisanhenol (3) were synthesized. The hepatoprotective effects of these dibenzocyclooctadiene lignan analogues against CCl4-induced injury were preliminarily evaluated. Most of the analogues exhibited higher protective effects than the positive control biphenyldicarboxylate (DDB). Among these active analogues, dichloroschisanhenol (3a) exhibited the strongest protective activity (cell survival rate exceeding 98.0%). |
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Keywords: | Schizandrin Schizandrin B Schisanhenol Dibenzocyclooctadiene lignan derivatives Hepatoprotective effect |
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