Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, Moscow 117997, Russia.
G.B. Elyakov Pacific Institute of Bioorganic Chemistry, Far Eastern Branch, Russian Academy of Sciences, Vladivostok 690022, Russia.
Int J Mol Sci. 2023 Nov 20;24(22):16514. doi: 10.3390/ijms242216514.
α-Amylase is a generally acknowledged molecular target of a distinct class of antidiabetic drugs named α-glucosidase inhibitors. This class of medications is scarce and rather underutilized, and treatment with current commercial drugs is accompanied by unpleasant adverse effects. However, mammalian α-amylase inhibitors are abundant in nature and form an extensive pool of high-affinity ligands that are available for drug discovery. Individual compounds and natural extracts and preparations are promising therapeutic agents for conditions associated with impaired starch metabolism, e.g., diabetes mellitus, obesity, and other metabolic disorders. This review focuses on the structural diversity and action mechanisms of active natural products with inhibitory activity toward mammalian α-amylases, and emphasizes proteinaceous inhibitors as more effective compounds with significant potential for clinical use.
α-淀粉酶是一类被称为α-葡萄糖苷酶抑制剂的独特降糖药物的公认分子靶标。这类药物稀缺且利用率较低,而目前商业药物的治疗伴随着不愉快的不良反应。然而,哺乳动物α-淀粉酶抑制剂在自然界中大量存在,并形成了广泛的高亲和力配体库,可用于药物发现。单个化合物、天然提取物和制剂是治疗淀粉代谢受损相关疾病(如糖尿病、肥胖症和其他代谢紊乱)的有前途的治疗药物。本文综述了具有抑制哺乳动物α-淀粉酶活性的天然产物的结构多样性和作用机制,并强调了蛋白质抑制剂作为更有效的化合物,具有重要的临床应用潜力。