PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
34162861-4	2021	We identify homoharringtonine and halofuginone as the most attractive agents, reducing endogenous TMPRSS2 expression at sub-micromolar concentrations.	halofuginone	34-46	transmembrane serine protease 2	Homo sapiens	98-105	
34162861-6	2021	We further demonstrate that halofuginone modulates TMPRSS2 levels through proteasomal-mediated degradation that involves the E3 ubiquitin ligase component DDB1- and CUL4-associated factor 1 (DCAF1).	halofuginone	28-40	transmembrane serine protease 2	Homo sapiens	51-58	
32818215-4	2020	Among these, homoharringtonine and halofuginone appear the most potent agents, reducing endogenous TMPRSS2 expression at sub-micromolar concentrations.	halofuginone	35-47	transmembrane serine protease 2	Homo sapiens	99-106	
32818215-6	2020	We further demonstrate that halofuginone modulates TMPRSS2 levels through proteasomal-mediated degradation that involves the E3 ubiquitin ligase component DDB1- and CUL4-associated factor 1 (DCAF1).	halofuginone	28-40	transmembrane serine protease 2	Homo sapiens	51-58