Adipocyte fatty acid binding protein 4 (FABP4) inhibitors. A comprehensive systematic review

被引:79
作者
Floresta, Giuseppe [1 ,2 ]
Pistara, Venerando [1 ]
Amata, Emanuele [1 ]
Dichiara, Maria [1 ]
Marrazzo, Agostino [1 ]
Prezzavento, Orazio [1 ]
Rescifina, Antonio [1 ]
机构
[1] Univ Catania, Dipartimento Sci Farmaco, I-95125 Catania, Italy
[2] Univ Catania, Dipartimento Sci Chim, I-95125 Catania, Italy
关键词
FABP4; A-FABP; aP2; Antidiabetes; Antiobesity; Antiatherosclerosis; ALPHA-GLUCOSIDASE; CRYSTAL-STRUCTURE; CELL-GROWTH; EXPRESSION; DISCOVERY; AFFINITY; PROMOTES; OBESITY; MODULATION; DESIGN;
D O I
10.1016/j.ejmech.2017.07.022
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Small molecule inhibitors of adipocyte fatty acid binding protein 4 (FABP4) have attracted interest following the recent publications of beneficial pharmacological effects of these compounds. FABP4 is predominantly expressed in macrophages and adipose tissue where it regulates fatty acids (FAs) storage and lipolysis and is an important mediator of inflammation. In the past years, hundreds FABP4 inhibitors have been synthesized for effective atherosclerosis and diabetes treatments, including derivatives of niacin, quinoxaline, aryl-quinoline, bicyclic pyridine, urea, aromatic compounds and other novel heterocyclic compounds. This review provides an overview of the synthesized and discovered molecules as adipocyte fatty acid binding protein 4 inhibitors (FABP4is) since the synthesis of the putative FABP4i, BMS309403, highlighting the interactions of the different classes of inhibitors with the targets. (C) 2017 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:854 / 873
页数:20
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