| Literature DB >> 28738306 |
Giuseppe Floresta1, Venerando Pistarà2, Emanuele Amata2, Maria Dichiara2, Agostino Marrazzo2, Orazio Prezzavento2, Antonio Rescifina3.
Abstract
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.Entities:
Keywords: A-FABP; Antiatherosclerosis; Antidiabetes; Antiobesity; FABP4; aP2
Mesh:
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Year: 2017 PMID: 28738306 DOI: 10.1016/j.ejmech.2017.07.022
Source DB: PubMed Journal: Eur J Med Chem ISSN: 0223-5234 Impact factor: 6.514