PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
9703439-1	1998	The effects of carbamate anticholinesterases, pyridostigmine and physostigmine, on the function of the nicotinic receptor (nAChR) in TE671 cells was studied, precluding their inhibition of acetylcholine hydrolysis by carbachol usage.	Carbamates	15-24	cholinergic receptor nicotinic alpha 4 subunit	Homo sapiens	123-128	
19027295-2	2009	The carbamate functionality and a small hydrophobic substituent in the C-3 position were found to be vital for the binding affinity to the nAChRs, whereas the carbamate nitrogen substituents were important for nAChR subtype selectivity.	Carbamates	4-13	cholinergic receptor nicotinic alpha 4 subunit	Homo sapiens	139-144	
18805006-1	2008	The synthesis and structure-activity relationship of a series of carbamate potentiators of alpha4beta2 nAChR is reported herein.	Carbamates	65-74	cholinergic receptor nicotinic alpha 4 subunit	Homo sapiens	103-108	
15336274-2	2004	Carbamate derivatives bearing a pyrrolidine or piperidine moiety 8-20 exhibited much lower affinity for alpha7* nAChR than the analogues in the quinuclidine series 21-25, although the same structural elements are present.	Carbamates	0-9	cholinergic receptor nicotinic alpha 4 subunit	Homo sapiens	104-117