PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
23641325-6	2013	For both the compounds, a concentration of 10 muM (equivalent to 1.88 mug/ml for plumbagin and 3.68 mug/ml for sanguinarine) resulted in 100% mortality at 48 h, which meets the World Health Organization"s (WHO) criterion of "hit" compounds for the control of schistosomiasis.	sanguinarine	111-123	latexin	Homo sapiens	46-49	
27420038-3	2016	Sanguinarine, chelerythrine and chelidonine depolymerized the microtubule network in living cancer cells (Hela cells and human osteosarcoma U2OS cells) and inhibited tubulin polymerization in vitro with IC50 values of 48.41 +- 3.73, 206.39 +- 4.20 and 34.51 +- 9.47 muM, respectively.	sanguinarine	0-12	latexin	Homo sapiens	266-269	
23500771-4	2013	The results showed that SAG was a potent noncompetitive inhibitor of CYP2C8 activity (Ki=8.9 muM), and competitive inhibitor of CYP1A2, CYP2C9 and CYP3A4 activities (Ki=2.7, 3.8 and 2.0 muM, respectively).	sanguinarine	24-27	latexin	Homo sapiens	93-96	
23500771-4	2013	The results showed that SAG was a potent noncompetitive inhibitor of CYP2C8 activity (Ki=8.9 muM), and competitive inhibitor of CYP1A2, CYP2C9 and CYP3A4 activities (Ki=2.7, 3.8 and 2.0 muM, respectively).	sanguinarine	24-27	latexin	Homo sapiens	186-189