PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
34709124-9	2021	Free energy calculations using Prime-MM/GBSA suggest that Celecoxib formed the most stable complex with TACE, followed by Glipizide, Sitagliptin, and Lapatinib.	Celecoxib	58-67	ADAM metallopeptidase domain 17	Homo sapiens	104-108	
34709124-5	2021	Based on docking energy (<= -9.00 kcal mol-1), four drugs (Celecoxib, Glipizide, Lapatinib, and Sitagliptin) were identified as potential inhibitors of TACE, with binding affinities up to 106-107 M-1.	Celecoxib	59-68	ADAM metallopeptidase domain 17	Homo sapiens	152-156