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Merck
CN

Alpha glucosidase inhibitors.

JPMA. The Journal of the Pakistan Medical Association (2014-05-29)
Sanjay Kalra
摘要

Alpha glucosidase inhibitors (AGIs) are a unique class of anti-diabetic drugs. Derived from bacteria, these oral drugs are enzyme inhibitors which do not have a pancreato -centred mechanism of action. Working to delay carbohydrate absorption in the gastrointestinal tract, they control postprandial hyperglycaemia and provide unquestioned cardiovascular benefit. Specially suited for a traditional Pakistani carbohydrate-rich diet, AGIs have been termed the 'untapped diamonds' of diabetology. The use of these oral antidiabetic drugs (OADs) that target pathophysiology in the early stages of type 2 diabetes, notably to reduce postprandial hyperglycaemia and hyperinsulinaemia will inevitably increase with time. This review describes the history of their development, mechanism of action, basic and clinical pharmacology, and suggests practical, evidence-based guidance for their optimal use.

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Sigma-Aldrich
阿卡波糖, ≥95% (HPLC)
Supelco
阿卡波糖, Pharmaceutical Secondary Standard; Certified Reference Material
阿卡波糖, European Pharmacopoeia (EP) Reference Standard
阿卡波糖, European Pharmacopoeia (EP) Reference Standard
阿卡波糖, European Pharmacopoeia (EP) Reference Standard