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