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Pharmacological Characterization of Bay G 5421, A Glucosidase Inhibitor for the Treatment of Carbohydrate-Dependent Metabolic Disorders

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Deutsche Pharmakologische Gesellschaft

Abstract

BAY g 5421* delays starch as well as sucrose digestion in the small intestine by inhibiting glucosidases involved in the hydrolysis of oligosaccharides. As a consequence in loading tests with both carbohydrates the blood glucose and serum insulin increments are reduced in animals and in man. The ED 50 is approximately 0.5–3 mg BAY g 5421/kg per os.

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© 1978 Springer-Verlag Berlin Heidelberg

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Puls, W., Keup, U., Krause, H.P., Thomas, G. (1978). Pharmacological Characterization of Bay G 5421, A Glucosidase Inhibitor for the Treatment of Carbohydrate-Dependent Metabolic Disorders. In: Deutsche Pharmakologische Gesellschaft. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-39532-5_28

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  • DOI: https://doi.org/10.1007/978-3-662-39532-5_28

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-662-38666-8

  • Online ISBN: 978-3-662-39532-5

  • eBook Packages: Springer Book Archive

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