PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
25747583-3	2015	In this study, we describe the discovery of a novel PKD small molecule inhibitor, SD-208, from a targeted kinase inhibitor library screen, and the synthesis of a series of analogs to probe the structure-activity relationship (SAR) vs. PKD1.	SD-208	82-88	polycystin 1, transient receptor potential channel interacting	Homo sapiens	235-239	
25747583-5	2015	Targeted inhibition of PKD by SD-208 resulted in potent inhibition of cell proliferation, an effect that could be reversed by overexpressed PKD1 or PKD3.	SD-208	30-36	polycystin 1, transient receptor potential channel interacting	Homo sapiens	140-144