PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
33896285-6	2021	We found that the highly active LTA4H inhibitors mostly contained diphenylmethane or diphenyl ether as the scaffold and pyridine or piperidine as the side chain.	piperidine	132-142	leukotriene A4 hydrolase	Homo sapiens	32-37	
20371179-0	2010	Discovery of novel leukotriene A4 hydrolase inhibitors based on piperidine and piperazine scaffolds.	piperidine	64-74	leukotriene A4 hydrolase	Homo sapiens	19-43	
20371179-1	2010	Novel piperidine and piperazine derivatives have been designed and tested as inhibitors of LTA(4) hydrolase (LTA(4)H).	piperidine	6-16	leukotriene A4 hydrolase	Homo sapiens	91-107	
20371179-1	2010	Novel piperidine and piperazine derivatives have been designed and tested as inhibitors of LTA(4) hydrolase (LTA(4)H).	piperidine	6-16	leukotriene A4 hydrolase	Homo sapiens	109-116	
20371179-3	2010	Crystallography studies further confirmed observed structure-activity relationship and LTA(4)H binding mode for analogs from the piperidine series.	piperidine	129-139	leukotriene A4 hydrolase	Homo sapiens	87-94