PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
35597409-19	2022	RESULTS: Berberine, jateorhizine, coptisine, epiberberine, columbamine, demethyleneberberine, and berberrubine could significantly inhibit hOCT1 and hOCT2 activity.	jatrorrhizine	20-32	solute carrier family 22 member 1	Homo sapiens	139-144	
26134304-7	2016	Additionally, coptisine, jatrorrhizine and epiberberine were substrates of all the hOCTs with the Km of 0.273-5.80 muM, whereas berberrubine was a substrate for hOCT1 and hOCT2, but not for hOCT3, the Km values were 1.27 and 1.66 muM, respectively.	jatrorrhizine	25-38	solute carrier family 22 member 1	Homo sapiens	161-166	
26134304-10	2016	The above data indicate that the tested alkaloids are potent inhibitors, and coptisine, jatrorrhizine, epiberberine and berberrubine are substrates of hOCT1, hOCT2 and/or hOCT3 with high affinity.	jatrorrhizine	88-101	solute carrier family 22 member 1	Homo sapiens	151-156	
35597409-20	2022	Isoquinoline alkaloids, including berberine, jateorhizine, coptisine, epiberberine, columbamine, and palmatine, were substrates of hOCT1 and hOCT2, but not the indole alkaloids evodiamine and rutaecarpine.	jatrorrhizine	45-57	solute carrier family 22 member 1	Homo sapiens	131-136