PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
20965230-0	2011	The natural compounds atraric acid and N-butylbenzene-sulfonamide as antagonists of the human androgen receptor and inhibitors of prostate cancer cell growth.	N-butylbenzenesulfonamide	39-65	androgen receptor	Homo sapiens	94-111
19914207-3	2010	We recently characterized iron-dependent toxic alpha-syn oligomer species by confocal single molecule fluorescence techniques and used this aggregation model to identify several N"-benzylidene-benzohydrazide (NBB) derivatives inhibiting oligomer formation in vitro.	N-butylbenzenesulfonamide	209-212	synuclein alpha	Homo sapiens	47-56
19914207-5	2010	Similar to our previous findings in vitro, we found a converse modulation of toxic alpha-syn oligomers by NBB derivates and ferric iron, which was characterized by an increase in aggregate formation by iron and an inhibitory effect of certain NBB compounds.	N-butylbenzenesulfonamide	106-109	synuclein alpha	Homo sapiens	83-92
19914207-5	2010	Similar to our previous findings in vitro, we found a converse modulation of toxic alpha-syn oligomers by NBB derivates and ferric iron, which was characterized by an increase in aggregate formation by iron and an inhibitory effect of certain NBB compounds.	N-butylbenzenesulfonamide	243-246	synuclein alpha	Homo sapiens	83-92
8588290-0	1995	Behavioral changes with alterations of choline acetyltransferase immunoreactivities induced by N-butyl benzenesulfonamide.	N-butylbenzenesulfonamide	95-121	choline O-acetyltransferase	Rattus norvegicus	39-64
21210660-8	2011	Pyrrole (8.26-39.21 ngN m(-3) air) and N-butyl-benzenesulfonamide (6.23-20.87 ngN m(-3) air) were the most abundant ON compounds observed in all samples analyzed.	N-butylbenzenesulfonamide	39-65	neogenin 1	Homo sapiens	78-81
21891864-1	2011	The structure activity relationship of N"-benzylidene-benzohydrazide (NBB) binding to tau and paired helical filament (PHF) proteins as well as amyloid-beta1-42 fibrils indicate differential selectivity for these protein aggregates.	N-butylbenzenesulfonamide	70-73	microtubule associated protein tau	Homo sapiens	86-89