Recent Developments in Sodium-Glucose Co-Transporter 2 (SGLT2) Inhibitors as a Valuable Tool in the Treatment of Type 2 Diabetes Mellitus

被引:8
作者
Kumar, Shubham [1 ]
Khatik, Gopal L. [1 ]
Mittal, Amit [1 ]
机构
[1] Lovely Profess Univ, Sch Pharmaceut Sci, Dept Pharmaceut Chem, Jalandhar Delhi GT Rd NH 1, Phagwara 144411, Punjab, India
关键词
Diabetes; Hyperglycemia; Hypoglycemic agents; Antidiabetic agents; hSGLT2; SGLT2; inhibitors; DUAL SGLT1/SGLT2 INHIBITOR; IMPROVED GLYCEMIC CONTROL; SERUM URIC-ACID; TRANSPORT; INSULIN; POTENT; EMPAGLIFLOZIN; DAPAGLIFLOZIN; CANAGLIFLOZIN; HYPERGLYCEMIA;
D O I
10.2174/1389557519666191009163519
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
In today's world, metabolic disorders are much dominant, and among them, diabetes is causing the highest rate of mortality. There is no cure for diabetes, while treatment could be done either by insulin therapy or oral antidiabetic drug. Oral antidiabetic agents target pathogenic factors like receptors, enzymes, genes and proteins involved in diabetes progression. Among them, recently, sodium-glucose co-transporters (SGLTs) have been recognized for their potential to effectively treat Type 2 diabetes mellitus. SGLTs are classified as SGLT-1 and SGLT-2, and among them, SGLT-2 is a major transporter which is involved in glucose reabsorption. Therefore, targeting SGLTs by its inhibitors could be a better choice to control the blood glucose level. Canagliflozin, dapagliflozin, empagliflozin, ipragliflozin, luseogliflozin, and tofogliflozin are known to be SGLT-2 inhibitors. Herein, we discussed the current and future aspects of the development and applications of SGLT-2 inhibitors.
引用
收藏
页码:170 / 182
页数:13
相关论文
共 95 条
[1]  
Abdul-Ghani Muhammad A, 2008, Endocr Pract, V14, P782
[2]  
[Anonymous], 2014, CANAGLIFLOZIN PRESCR
[3]  
[Anonymous], DIAB FACT SHEET
[4]   Effects of chronic treatment with noradrenaline or a specific β3-adrenergic agonist, CL 316,243, on energy expenditure and epididymal adipocyte lipolytic activity in rat [J].
Atgié, C ;
Faintrenie, G ;
Carpéné, C ;
Bukowiecki, LJ ;
Géloën, A .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY A-MOLECULAR & INTEGRATIVE PHYSIOLOGY, 1998, 119 (02) :629-636
[5]   DIFFERENCES IN ACTIVE AND PASSIVE GLUCOSE-TRANSPORT ALONG THE PROXIMAL NEPHRON [J].
BARFUSS, DW ;
SCHAFER, JA .
AMERICAN JOURNAL OF PHYSIOLOGY, 1981, 241 (03) :F322-F332
[6]   Estrogen receptors:: new players in diabetes mellitus [J].
Barros, Rodrigo P. A. ;
Machado, Ubiratan Fabres ;
Gustafsson, Jan-Ake .
TRENDS IN MOLECULAR MEDICINE, 2006, 12 (09) :425-431
[7]   Modeling and informatics in designing anti-diabetic agents [J].
Bharatam, P. V. ;
Patel, D. S. ;
Adane, L. ;
Mittal, A. ;
Sundriyal, S. .
CURRENT PHARMACEUTICAL DESIGN, 2007, 13 (34) :3518-3530
[8]   Modification on the O-glucoside of Sergliflozin-A: A new strategy for SGLT2 inhibitor design [J].
Cao, Xuefeng ;
Zhang, Wenpeng ;
Yan, Xu ;
Huang, Zhi ;
Zhang, Zhenqing ;
Wang, Peng ;
Shen, Jie .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2016, 26 (09) :2170-2173
[9]  
Chakrabarti R, 2002, CURR SCI INDIA, V83, P1533
[10]   SGLT2 inhibition - a novel strategy for diabetes treatment [J].
Chao, Edward C. ;
Henry, Robert R. .
NATURE REVIEWS DRUG DISCOVERY, 2010, 9 (07) :551-559