PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
9836623-8	1998	SAR studies revealed that the pyridine nitrogen atom and the nature and the position of the substituents on the pyridine ring were critically involved in the ability of the compounds to recognize and activate 5-HT1A receptors.	pyridine	30-38	5-hydroxytryptamine receptor 1A	Homo sapiens	209-215	
20580787-1	2010	A novel pyridine derivative, 8-{4-[(6-methoxy-2,3-dihydro-[1,4]dioxino[2,3-b]pyridine-3-ylmethyl)-amino]-butyl}-8-aza-spiro[4.5]decane-7,9-dione hydrochloride, termed JB-788, was designed to selectively target 5-HT(1A) receptors.	pyridine	8-16	5-hydroxytryptamine receptor 1A	Homo sapiens	210-217	
9836623-8	1998	SAR studies revealed that the pyridine nitrogen atom and the nature and the position of the substituents on the pyridine ring were critically involved in the ability of the compounds to recognize and activate 5-HT1A receptors.	pyridine	112-120	5-hydroxytryptamine receptor 1A	Homo sapiens	209-215	
7473547-11	1995	The CAR activities of pyrroles 6 and 12, thiophene 40, furans 44-47, isoxazolines 49 and 50, and pyridine 54 coupled with their weak or nonexistent D2 binding and strong 5-HT1A binding suggest that they may be acting via a nondopaminergic mechanism or that dopaminergic active metabolites are responsible.	pyridine	97-105	5-hydroxytryptamine receptor 1A	Homo sapiens	170-176