PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
26174773-4	2015	Cys residues were introduced at 12 positions in hSERT to enable covalent attachment of a rhodamine-based fluorophore.	Rhodamines	89-98	solute carrier family 6 member 4	Homo sapiens	48-53	
24944746-1	2014	Novel rhodamine-labeled ligands, based on (S)-citalopram, were synthesized and evaluated for uptake inhibition at the human serotonin, dopamine, and norepinephrine transporters (hSERT, hDAT, and hNET, respectively) and for binding at SERT, in transiently transfected COS7 cells.	Rhodamines	6-15	solute carrier family 6 member 4	Homo sapiens	179-183	
23168018-0	2013	A rhodamine-labeled citalopram analogue as a high-affinity fluorescent probe for the serotonin transporter.	Rhodamines	2-11	solute carrier family 6 member 4	Homo sapiens	85-106	
23168018-3	2013	The resulting rhodamine-labeled ligand 8 inhibited [(3)H]5-HT uptake in COS-7 cells (K(i)=225 nM) with similar potency to the tropane-based JHC 1-064 (1), but with higher specificity towards the SERT relative to the transporters for dopamine and norepinephrine.	Rhodamines	14-23	solute carrier family 6 member 4	Homo sapiens	195-199