PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
20674099-5	2010	We conclude that these indole and benzofuran derivatives are promising reversible MAO-B inhibitors with a possible role in the treatment of neurodegenerative diseases such as Parkinson"s disease (PD).	benzofuran	34-44	monoamine oxidase B	Homo sapiens	82-87	
23589499-5	2013	5-Nitro-2-(4-methoxyphenyl)benzofuran (8) is the most active compound of the benzofuran series, presenting MAO-B selectivity and reversible inhibition (IC50 =140 nM).	benzofuran	27-37	monoamine oxidase B	Homo sapiens	107-112	
34771054-5	2021	Based on this view, new benzofuran/benzothiophene and thiosemicarbazone hybrid compounds were synthesized, characterized and screened for their hMAO-A and hMAO-B inhibitory activity by an in vitro fluorometric method.	benzofuran	24-34	monoamine oxidase B	Homo sapiens	155-161	
33444985-3	2021	Substitution patterns on both the phenyl ring and the benzofuran moiety determine the affinity for MAO-A or MAO-B.	benzofuran	54-64	monoamine oxidase B	Homo sapiens	108-113