PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
12766255-8	2003	Thus, the simplified N-n-alkylpyridinium analogs are potent, selective, and competitive antagonists of nAChRs mediating nicotine-evoked [3H]DA overflow, indicating that the N-methylpyrrolidino moiety is not a structural requirement for interaction with nAChR subtypes mediating nicotine-evoked DA release.	amsonic acid	140-142	cholinergic receptor nicotinic beta 1 subunit	Rattus norvegicus	103-108	
17207584-9	2007	These data indicate that the selective DA uptake inhibitor GBR-12909 is able to inhibit nAChRs, that is, the nAChR antagonistic property of monoamine uptake inhibitors is independent of their selectivity.	amsonic acid	39-41	cholinergic receptor nicotinic beta 1 subunit	Rattus norvegicus	88-93