J. Tilley, J. Grimsby, S. Erickson, Berthel Steven Joseph
{"title":"糖尿病药物:现在的和新兴的","authors":"J. Tilley, J. Grimsby, S. Erickson, Berthel Steven Joseph","doi":"10.1002/0471266949.BMC198","DOIUrl":null,"url":null,"abstract":"This chapter includes a summary of the mechanism of action, history, and ADME properties compounds selected from four classes of marketed drugs for the treatment of type 2 diabetes. These include the biguanides (metformin), α-glucosylase inhibitors, sulfonylureas, and glinides. In addition, a discussion of several advanced, emerging classes of drugs together with lead structures is provided. The mechanistic classes of emerging drugs include inhibitors of the sodium glucose cotransporter 2 (SGLT2), glucokinase activators (GKAs), inhibitors of fructose-1,6-bisphosphatase (FPase), inhibitors of 11-β-sterol dehydrogenase (11-β-HSD1), agonists acting on the G-coupled-protein receptor GPR119, and mimics of the sirtuin family member SIRT1. \n \n \nKeywords: \n \ndiabetes; \nglucokinase; \nmetformin; \nsodium glucose cotransporter; \nsalfonyl urea","PeriodicalId":9514,"journal":{"name":"Burger's Medicinal Chemistry and Drug Discovery","volume":"16 1","pages":"1-38"},"PeriodicalIF":0.0000,"publicationDate":"2010-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"4","resultStr":"{\"title\":\"Diabetes Drugs: Present and Emerging\",\"authors\":\"J. Tilley, J. Grimsby, S. Erickson, Berthel Steven Joseph\",\"doi\":\"10.1002/0471266949.BMC198\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"This chapter includes a summary of the mechanism of action, history, and ADME properties compounds selected from four classes of marketed drugs for the treatment of type 2 diabetes. These include the biguanides (metformin), α-glucosylase inhibitors, sulfonylureas, and glinides. In addition, a discussion of several advanced, emerging classes of drugs together with lead structures is provided. The mechanistic classes of emerging drugs include inhibitors of the sodium glucose cotransporter 2 (SGLT2), glucokinase activators (GKAs), inhibitors of fructose-1,6-bisphosphatase (FPase), inhibitors of 11-β-sterol dehydrogenase (11-β-HSD1), agonists acting on the G-coupled-protein receptor GPR119, and mimics of the sirtuin family member SIRT1. \\n \\n \\nKeywords: \\n \\ndiabetes; \\nglucokinase; \\nmetformin; \\nsodium glucose cotransporter; \\nsalfonyl urea\",\"PeriodicalId\":9514,\"journal\":{\"name\":\"Burger's Medicinal Chemistry and Drug Discovery\",\"volume\":\"16 1\",\"pages\":\"1-38\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2010-09-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"4\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Burger's Medicinal Chemistry and Drug Discovery\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1002/0471266949.BMC198\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Burger's Medicinal Chemistry and Drug Discovery","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/0471266949.BMC198","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
This chapter includes a summary of the mechanism of action, history, and ADME properties compounds selected from four classes of marketed drugs for the treatment of type 2 diabetes. These include the biguanides (metformin), α-glucosylase inhibitors, sulfonylureas, and glinides. In addition, a discussion of several advanced, emerging classes of drugs together with lead structures is provided. The mechanistic classes of emerging drugs include inhibitors of the sodium glucose cotransporter 2 (SGLT2), glucokinase activators (GKAs), inhibitors of fructose-1,6-bisphosphatase (FPase), inhibitors of 11-β-sterol dehydrogenase (11-β-HSD1), agonists acting on the G-coupled-protein receptor GPR119, and mimics of the sirtuin family member SIRT1.
Keywords:
diabetes;
glucokinase;
metformin;
sodium glucose cotransporter;
salfonyl urea