PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
28094183-0	2017	Discovering novel 7-azaindole-based series as potent AXL kinase inhibitors.	7-azaindole dimer	18-29	AXL receptor tyrosine kinase	Homo sapiens	53-56	
28094183-3	2017	In this context, we started to design new kinase inhibitors targeting AXL from the 7-azaindole scaffold well known to interact with the ATP binding site of the kinase.	7-azaindole dimer	83-94	AXL receptor tyrosine kinase	Homo sapiens	70-73	
28094183-4	2017	Focused screening and chemical diversification around 7-azaindole scaffold were developed, based on modeling studies and medicinal chemistry rational, leading to the discovery of a new family of hits with potent inhibitory activity against AXL.	7-azaindole dimer	54-65	AXL receptor tyrosine kinase	Homo sapiens	240-243