PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
33360082-3	2021	Aiming at the elucidation of MAO-B inhibitors with 1,3,4-oxadiazole scaffolds, we make a comprehensive update on the new and old chemical methods employed for the synthesis of the unsymmetrical oxadiazole derivatives that lead to high yield compounds.	Oxadiazoles	57-67	monoamine oxidase B	Homo sapiens	29-34	
33360082-4	2021	We summarize a state of the selective MAO-B inhibitors with oxadiazole scaffold, describing the results, structures, structure-activity relationships (SARs) and medicinal chemistry strategies over the years.	Oxadiazoles	60-70	monoamine oxidase B	Homo sapiens	38-43	
33360082-5	2021	The analysis of the recent papers would facilitate tracking the increasing number of oxadiazole derivatives as new chemical spaces with MAO-B inhibitory potential designed to ensure the safe use of the compounds and elimination of the unwanted drug-drug interactions.	Oxadiazoles	85-95	monoamine oxidase B	Homo sapiens	136-141