PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
34075338-0	2021	Structural insights and inhibition mechanism of TMPRSS2 by experimentally known inhibitors Camostat mesylate, Nafamostat and Bromhexine hydrochloride to control SARS-coronavirus-2: A molecular modeling approach.	Bromhexine	125-149	transmembrane serine protease 2	Homo sapiens	48-55	
34075338-5	2021	Hence, we have used a molecular dynamics (MD) simulated homology model of TMPRSS2 to study the inhibition mechanism of experimentally known inhibitors Camostat mesylate, Nafamostat and Bromhexine hydrochloride (BHH) using molecular modeling techniques.	Bromhexine	185-209	transmembrane serine protease 2	Homo sapiens	74-81	
34075338-5	2021	Hence, we have used a molecular dynamics (MD) simulated homology model of TMPRSS2 to study the inhibition mechanism of experimentally known inhibitors Camostat mesylate, Nafamostat and Bromhexine hydrochloride (BHH) using molecular modeling techniques.	Bromhexine	211-214	transmembrane serine protease 2	Homo sapiens	74-81	
34075338-7	2021	Molecular docking analysis revealed that Camostat mesylate and its structural analogue Nafamostat interact strongly with residues His296 and Ser441 present in the catalytic triad of TMPRSS2, whereas BHH binds with Ala386 along with other residues.	Bromhexine	199-202	transmembrane serine protease 2	Homo sapiens	182-189