PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
34209843-1	2021	In the search for new chemical scaffolds able to afford NLRP3 inflammasome inhibitors, we used a pharmacophore-hybridization strategy by combining the structure of the acrylic acid derivative INF39 with the 1-(piperidin-4-yl)1,3-dihydro-2H-benzo(d)imidazole-2-one substructure present in HS203873, a recently identified NLRP3 binder.	1-(piperidin-4-yl)1,3-dihydro-2h-benzo(d)imidazole-2-one	207-263	NLR family pyrin domain containing 3	Homo sapiens	56-61	
34209843-1	2021	In the search for new chemical scaffolds able to afford NLRP3 inflammasome inhibitors, we used a pharmacophore-hybridization strategy by combining the structure of the acrylic acid derivative INF39 with the 1-(piperidin-4-yl)1,3-dihydro-2H-benzo(d)imidazole-2-one substructure present in HS203873, a recently identified NLRP3 binder.	1-(piperidin-4-yl)1,3-dihydro-2h-benzo(d)imidazole-2-one	207-263	NLR family pyrin domain containing 3	Homo sapiens	320-325