PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 25441945-8 2014 Moreover, we described for the first time the binding mode of TZDs in the binding site of FFAR1. Thiazolidinediones 62-66 free fatty acid receptor 1 Homo sapiens 90-95 26774923-0 2016 Design, synthesis, and biological evaluation of novel thiazolidinediones as PPARgamma/FFAR1 dual agonists. Thiazolidinediones 54-72 free fatty acid receptor 1 Homo sapiens 86-91 26774923-6 2016 It has been reported that some thiazolidinediones (TZDs) activate FFAR1 with micromolar potency. Thiazolidinediones 31-49 free fatty acid receptor 1 Homo sapiens 66-71 33100202-8 2021 Most of the small molecule FFAR1/GPR40 agonists developed were aryl alkanoic acid derivatives (such as phenylpropionic acids, phenylacetic acids, phenoxyacetic acids and benzofuran acetic acid derivatives) and thiazolidinediones. Thiazolidinediones 210-228 free fatty acid receptor 1 Homo sapiens 27-32 25441945-0 2014 Homology modeling and explicit membrane molecular dynamics simulation to delineate the mode of binding of thiazolidinediones into FFAR1 and the mechanism of receptor activation. Thiazolidinediones 106-124 free fatty acid receptor 1 Homo sapiens 130-135 25441945-4 2014 It was reported that some thiazolidinediones (TZDs), the best studied PPARgamma agonists, are also able to stimulate FFAR1 in a dose-dependent manner. Thiazolidinediones 26-44 free fatty acid receptor 1 Homo sapiens 117-122 25441945-4 2014 It was reported that some thiazolidinediones (TZDs), the best studied PPARgamma agonists, are also able to stimulate FFAR1 in a dose-dependent manner. Thiazolidinediones 46-50 free fatty acid receptor 1 Homo sapiens 117-122 19398560-2 2009 However, a range of selective, small molecule ligands have recently been developed as tool compounds to explore the therapeutic potential of this receptor, whereas clinically employed thiazolidinedione "glitazone" drugs are also agonists at FFA1. Thiazolidinediones 203-212 free fatty acid receptor 1 Homo sapiens 241-245 34133753-0 2021 Thiazolidinediones (TZDs) enhance insulin secretory response via GPR40 and adenylate cyclase (AC). Thiazolidinediones 0-18 free fatty acid receptor 1 Homo sapiens 65-70 34133753-0 2021 Thiazolidinediones (TZDs) enhance insulin secretory response via GPR40 and adenylate cyclase (AC). Thiazolidinediones 20-24 free fatty acid receptor 1 Homo sapiens 65-70 19346435-0 2009 Thiazolidinediones induce proliferation of human bronchial epithelial cells through the GPR40 receptor. Thiazolidinediones 0-18 free fatty acid receptor 1 Homo sapiens 88-93 17987108-1 2007 BACKGROUND: The FFAR1 receptor is expressed mainly in pancreatic beta cells and is activated by medium to long chain free fatty acids (FFAs), as well as by thiazolidinediones, resulting in elevated Ca(2+) concentrations and promotion of insulin secretion. Thiazolidinediones 156-174 free fatty acid receptor 1 Homo sapiens 16-21