PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
10037500-0	1999	Effects of methylphenidate analogues on phenethylamine substrates for the striatal dopamine transporter: potential as amphetamine antagonists?	phenethylamine	40-54	solute carrier family 6 member 3	Homo sapiens	83-103	
31265842-6	2019	beta-phenethylamine was the most potent, with IC50 values of 0.05 and 1.8 muM at the NET and DAT, respectively.	phenethylamine	0-19	solute carrier family 6 member 3	Homo sapiens	93-96	
20067583-4	2010	One compound bearing two dopamine (DA)-like pharmacophoric "heads" separated by an 8-carbon linker achieved an 82-fold gain in inhibition of [(3)H] 2beta-carbomethoxy-3beta-(4-fluorophenyl)-tropane (CFT) binding compared with DA itself; bivalent compounds with a 6-carbon linker and heterologous combinations of DA-, amphetamine- and beta-phenethylamine-like heads all resulted in considerable and comparable gains in DAT affinity.	phenethylamine	334-353	solute carrier family 6 member 3	Homo sapiens	418-421	
19519772-3	2009	The potency of p-tyramine and other non-catechols (d-amphetamine, beta-phenethylamine, MPP(+)) in inhibiting cocaine analog binding to DAT in digitonin-treated cells was markedly weakened to a level similar to that observed in cell-free membranes.	phenethylamine	66-85	solute carrier family 6 member 3	Homo sapiens	135-138