J. Tilley, J. Grimsby, S. Erickson, Berthel Steven Joseph
{"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}
引用次数: 4
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.
Keywords:
diabetes;
glucokinase;
metformin;
sodium glucose cotransporter;
salfonyl urea