PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
28858478-0	2017	Bisphenol AF and Bisphenol B Exert Higher Estrogenic Effects than Bisphenol A via G Protein-Coupled Estrogen Receptor Pathway.	bisphenol B	17-28	G protein-coupled estrogen receptor 1	Homo sapiens	82-117	
28858478-4	2017	Here, using a SKBR3 cell-based fluorescence competitive binding assay, we found six BPA analogues bound to GPER directly, with bisphenol AF (BPAF) and bisphenol B (BPB) displaying much higher (~9-fold) binding affinity than BPA.	bisphenol B	151-162	G protein-coupled estrogen receptor 1	Homo sapiens	107-111	
28858478-4	2017	Here, using a SKBR3 cell-based fluorescence competitive binding assay, we found six BPA analogues bound to GPER directly, with bisphenol AF (BPAF) and bisphenol B (BPB) displaying much higher (~9-fold) binding affinity than BPA.	bisphenol B	164-167	G protein-coupled estrogen receptor 1	Homo sapiens	107-111	
28858478-8	2017	Moreover, based on the results of Boyden chamber and wound-healing assays, BPAF and BPB displayed higher activity in promoting GPER mediated SKBR3 cell migration than BPA with the LOEC of 100 nM.	bisphenol B	84-87	G protein-coupled estrogen receptor 1	Homo sapiens	127-131	
28858478-9	2017	Overall, we found two BPA analogues BPAF and BPB could exert higher estrogenic effects than BPA via GPER pathway at nanomolar concentrations.	bisphenol B	45-48	G protein-coupled estrogen receptor 1	Homo sapiens	100-104