Fructose-1,6-bisphosphatase Inhibitors: A Review of Recent (2000-2017) Advances and Structure-Activity Relationship Studies

被引:1
作者
Singh, Sarbjit [1 ]
Harmalkar, Dipesh S. [1 ]
Choi, Yongseok [2 ]
Lee, Kyeong [1 ]
机构
[1] Dongguk Univ Seoul, Coll Pharm, Goyang 10326, South Korea
[2] Korea Univ, Coll Life Sci & Biotechnol, Seoul 02841, South Korea
基金
新加坡国家研究基金会;
关键词
Fructose-1,6-bisphosphatase inhibitors; type; 2; diabetes; adenosine 5 '-monophosphate; hyperglycemia; diabetes mellitus; chronic disease; FRUCTOSE 1,6-BISPHOSPHATASE; ALLOSTERIC INHIBITORS; BENZOXAZOLE BENZENESULFONAMIDES; HEPATIC GLUCONEOGENESIS; BIOLOGICAL EVALUATION; DESIGN; ACID; DERIVATIVES; DISCOVERY; POTENT;
D O I
10.2174/0929867325666180831133734
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Diabetes mellitus, commonly referred to as diabetes, is the 8th leading cause of death worldwide. As of 2015, approximately 415 million people were estimated to be diabetic worldwide, type 2 diabetes being the most common accounting for approximately 90-95% of all diagnosed cases with increasing prevalence. Fructose-1,6-bisphosphatase is one of the important therapeutic targets recently discovered to treat this chronic disease. In this focused review, we have highlighted recent advances and structure-activity relationship studies in the discovery and development of different fructose-1,6-bisphosphatase inhibitors reported since the year 2000.
引用
收藏
页码:5542 / 5563
页数:22
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