PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
1672380-4	1991	The selective 5-HT1A agonist, (+-)-8-hydroxy-diprolaminotetralin HBr (8-OH-DPAT), dose-dependently antagonized morphine-induced antinociception (MIA) without affecting the latency to respond when applied alone.	8-Hydroxy-2-(di-n-propylamino)tetralin	70-79	5-hydroxytryptamine (serotonin) receptor 1A	Mus musculus	14-20	
1672380-9	1991	The antagonism of MIA by 8-OH-DPAT was mimicked by additional drugs acting as high efficacy 5-HT1A agonists: lisuride, 5-methoxy-N,N-dimethyltryptamine hydrogen oxalate, RU 24969 [methoxy-3-(1,2,3.6-tetrahydropyridin-4-yl)-1H-indole] and d-lysergic acid diethylamide.	8-Hydroxy-2-(di-n-propylamino)tetralin	25-34	5-hydroxytryptamine (serotonin) receptor 1A	Mus musculus	92-98