PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
21134756-1	2011	Previous studies have shown that (E)-5-styrylisatin and (E)-6-styrylisatin are reversible inhibitors of human monoamine oxidase (MAO) A and B.	(E)-5-Styrylisatin	33-51	monoamine oxidase A	Homo sapiens	110-141
21134756-2	2011	Both homologues are reported to exhibit selective binding to the MAO-B isoform with (E)-5-styrylisatin being the most potent inhibitor.	(E)-5-Styrylisatin	84-102	monoamine oxidase B	Homo sapiens	65-70
21134756-6	2011	The most potent MAO-B inhibitor, 5-(4-phenylbutyl)isatin, exhibited an IC(50) value of 0.66nM, approximately 13-fold more potent than (E)-5-styrylisatin and 18,500-fold more potent than isatin.	(E)-5-Styrylisatin	134-152	monoamine oxidase B	Homo sapiens	16-21
19342233-4	2009	The (E)-5-styrylisatin analogues bound more tightly than the (E)-6 analogue although the latter exhibits the highest MAO-B selectivity.	(E)-5-Styrylisatin	4-22	monoamine oxidase B	Homo sapiens	117-122