PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
22687491-7	2012	Dose response curves at moderate [alphaKG] ([alphaKG]~K(M)) showed that the hydroxypyrones/hydroxypyridinones were selective inhibitors, with IC(50) in the muM range, and that the catechols were generally strong inhibitors of both FIH and PHD2, with IC(50) in the low muM range.	1-hydroxy-2(1H)-pyridinone	91-109	latexin	Homo sapiens	156-159	
22687491-7	2012	Dose response curves at moderate [alphaKG] ([alphaKG]~K(M)) showed that the hydroxypyrones/hydroxypyridinones were selective inhibitors, with IC(50) in the muM range, and that the catechols were generally strong inhibitors of both FIH and PHD2, with IC(50) in the low muM range.	1-hydroxy-2(1H)-pyridinone	91-109	latexin	Homo sapiens	268-271