PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
31514980-1	2019	Current study systematically investigated the interaction of two alkaloids, anisodine and monocrotaline, with organic cation transporter OCT1, 2, 3, MATE1 and MATE2-K by using in vitro stably transfected HEK293 cells.	Monocrotaline	90-103	solute carrier family 22 member 1	Homo sapiens	137-147	
31514980-5	2019	Monocrotaline was determined to be a substrate of both OCT1 (Km = 109.1 +- 17.8 micromol L-1, Vmax = 576.5 +- 87.5 pmol/mg protein/min) and OCT2 (Km = 64.7 +- 14.8 micromol L-1, Vmax = 180.7 +- 22.0 pmol/mg protein/min), other than OCT3 and MATE transporters.	Monocrotaline	0-13	solute carrier family 22 member 1	Homo sapiens	55-59	
23831208-6	2013	Moreover, the OCT1 inhibitors, such as quinidine, d-tetrahydropalmatine (d-THP), obviously inhibited the uptake of MCT in MDCK-hOCT1 cells and isolated rat primary hepatocytes, and attenuated the viability reduction and LDH release of the primary cultured rat hepatocytes caused by MCT.	Monocrotaline	115-118	solute carrier family 22 member 1	Homo sapiens	127-132