PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
24863930-6	2014	Furthermore, a large conductance nonspecific cation channel, which was identified previously in the vesicle membrane and has biophysical properties similar to that of an RyR, is pharmacologically affected in a manner characteristic of an RyR: it is activated in the presence of the RyR agonist ryanodine (at low concentrations) and blocked by the RyR antagonist ruthenium red.	Ruthenium Red	362-375	ryanodine receptor 1, skeletal muscle	Mus musculus	170-173	
24863930-6	2014	Furthermore, a large conductance nonspecific cation channel, which was identified previously in the vesicle membrane and has biophysical properties similar to that of an RyR, is pharmacologically affected in a manner characteristic of an RyR: it is activated in the presence of the RyR agonist ryanodine (at low concentrations) and blocked by the RyR antagonist ruthenium red.	Ruthenium Red	362-375	ryanodine receptor 1, skeletal muscle	Mus musculus	238-241	
9611131-3	1998	cADPR (10 nM-10 microM) induced a dose-dependent increase in [Ca2+]i, which was blocked by the cADPR receptor antagonist 8-amino-cADPR (20 microM) and by the RyR blockers ruthenium red (10 microM) and ryanodine (10 microM), but not by the inositol 1,4,5-trisphosphate receptor blocker heparin (0.5 mg/ml).	Ruthenium Red	171-184	ryanodine receptor 1, skeletal muscle	Mus musculus	158-161	
9142939-6	1997	In contrast, ruthenium red, a RyR antagonist, completely abolished ACh-induced [Ca2+]i oscillations.	Ruthenium Red	13-26	ryanodine receptor 1, skeletal muscle	Mus musculus	30-33	
24863930-6	2014	Furthermore, a large conductance nonspecific cation channel, which was identified previously in the vesicle membrane and has biophysical properties similar to that of an RyR, is pharmacologically affected in a manner characteristic of an RyR: it is activated in the presence of the RyR agonist ryanodine (at low concentrations) and blocked by the RyR antagonist ruthenium red.	Ruthenium Red	362-375	ryanodine receptor 1, skeletal muscle	Mus musculus	238-241	
24863930-6	2014	Furthermore, a large conductance nonspecific cation channel, which was identified previously in the vesicle membrane and has biophysical properties similar to that of an RyR, is pharmacologically affected in a manner characteristic of an RyR: it is activated in the presence of the RyR agonist ryanodine (at low concentrations) and blocked by the RyR antagonist ruthenium red.	Ruthenium Red	362-375	ryanodine receptor 1, skeletal muscle	Mus musculus	238-241	
15036951-4	2004	FK506-induced [Ca(2+)](i) increase was completely blocked by the RyR antagonist ruthenium red and ryanodine, but not the IP(3)R antagonist heparin.	Ruthenium Red	80-93	ryanodine receptor 1, skeletal muscle	Mus musculus	65-68	
10807666-5	2000	Sanguinarine induced Ca(2+) release from the actively loaded SR vesicles was blocked by ruthenium red and dithiothreitol (DTT), consistent with the ryanodine receptor (RyR) as the site of sanguinarine action.	Ruthenium Red	88-101	ryanodine receptor 1, skeletal muscle	Mus musculus	168-171