PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
34128259-0	2021	Design, synthesis, and biological evaluation of novel benzimidazole derivatives as sphingosine kinase 1 inhibitor.	benzimidazole	54-67	sphingosine kinase 1	Homo sapiens	83-103	
34128259-4	2021	Our design strategy is twofold: It aimed first to study the effect of replacing the 5-position of the benzimidazole ring with a polar carboxylic acid group on the SphK1-inhibitory activity and cytotoxicity.	benzimidazole	102-115	sphingosine kinase 1	Homo sapiens	163-168	
34128259-7	2021	The binding affinity of the benzimidazole derivatives toward SphK1 was measured by fluorescence binding and molecular docking.	benzimidazole	28-41	sphingosine kinase 1	Homo sapiens	61-66