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C14-Labeled Cardiac Glycosides
1966An essential structural and pharmacological characteristic of cardenolides is an a, s-unsaturated γ-lactone ring (the butenolide ring) in the 17 β-position. Ruzicka, Reichstein, and Furst [1] and others [2–5] first demonstrated the possibility of its synthesis from steroids other than cardenolides by means of the Reformatsky reaction [6,7]. By reaction
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The role of cardiac rehabilitation in improving cardiovascular outcomes
Nature Reviews Cardiology, 2021Rodney Taylor +2 more
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Cardiotoxicity of anticancer treatments: Epidemiology, detection, and management
Ca-A Cancer Journal for Clinicians, 2016Giuseppe Curigliano +2 more
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Adverse cardiac effects of cancer therapies: cardiotoxicity and arrhythmia
Nature Reviews Cardiology, 2020Joerg Herrmann
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