PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
26925138-2	2016	Given that flufenamic acid (FFA) blocks TRPM2 cation channels, resulting in reduced neuronal excitability, we aimed to investigate whether FFA suppresses the behavioral manifestation of sodium salicylate (SSA)-induced tinnitus in rats.	Flufenamic Acid	11-26	transient receptor potential cation channel, subfamily M, member 2	Rattus norvegicus	40-45	
26925138-2	2016	Given that flufenamic acid (FFA) blocks TRPM2 cation channels, resulting in reduced neuronal excitability, we aimed to investigate whether FFA suppresses the behavioral manifestation of sodium salicylate (SSA)-induced tinnitus in rats.	Flufenamic Acid	28-31	transient receptor potential cation channel, subfamily M, member 2	Rattus norvegicus	40-45	
21900507-8	2011	These responses were strongly inhibited by the nonselective TRPM2 channel blockers clotrimazole and flufenamic acid.	Flufenamic Acid	100-115	transient receptor potential cation channel, subfamily M, member 2	Rattus norvegicus	60-65	
21509529-0	2011	Aminoethoxydiphenyl borate and flufenamic acid inhibit Ca2+ influx through TRPM2 channels in rat dorsal root ganglion neurons activated by ADP-ribose and rotenone.	Flufenamic Acid	31-46	transient receptor potential cation channel, subfamily M, member 2	Rattus norvegicus	75-80	
21512734-1	2011	Melastatin-like transient receptor potential 2 (TRPM2) channel activation/inhibition mechanisms in response to ADP-ribose (ADPR), oxidative stress, flufenamic acid (FFA) and 2-aminoethoxydiphenyl borate (2-APB) are not clear.	Flufenamic Acid	148-163	transient receptor potential cation channel, subfamily M, member 2	Rattus norvegicus	48-53	
21512734-2	2011	We tested the effects of FFA and 2-APB on ADPR-induced TRPM2 cation channel currents in rat native bone marrow megakaryocytes.	Flufenamic Acid	25-28	transient receptor potential cation channel, subfamily M, member 2	Rattus norvegicus	55-60	
21509529-4	2011	Melastatin-like transient receptor potential 2 (TRPM2) channel activation and inhibition in response to oxidative stress, ADP-ribose (ADPR), flufenamic acid (FFA) and 2-aminoethoxydiphenyl borate (2-APB) in DRG neurons are also not clear.	Flufenamic Acid	141-156	transient receptor potential cation channel, subfamily M, member 2	Rattus norvegicus	48-53	
15275834-0	2004	Flufenamic acid is a pH-dependent antagonist of TRPM2 channels.	Flufenamic Acid	0-15	transient receptor potential cation channel, subfamily M, member 2	Rattus norvegicus	48-53