PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
28237803-4	2017	ACh-induced [Ca2+]i increases in chromaffin cells were also inhibited by the 5-HT1A receptor agonist, 8-hydroxy-2-(dipropylamino) tetralin hydrobromide, but were not changed by the 5-HT1B, 5-HT2, or 5-HT3 receptor agonists, CP93129, alpha-methyl-5-HT, or 1-(m-chlorophenyl) biguanide, respectively.	8-Hydroxy-2-(di-n-propylamino)tetralin	102-151	5-hydroxytryptamine receptor 3A	Rattus norvegicus	199-213	
9351653-6	1997	This inhibition was mimicked by N-(3-trifluoromethylphenyl)piperazine (TFMPP), a general serotonin receptor agonist, by 8-hydroxy-dipropylaminotetralin (8-OH-DPAT), a selective 5-HT1A receptor agonist, but not by phenylbiguanide, a 5-HT3 receptor agonist.	8-Hydroxy-2-(di-n-propylamino)tetralin	153-162	5-hydroxytryptamine receptor 3A	Rattus norvegicus	232-246	
8201242-4	1993	Using measurements of rodent behaviour in the mouse light and dark test box and rat social interaction, anxiolytic agents such as diazepam and putative anxiolytic agents such as the 5-HT1A and 5-HT3 receptor ligands 8-OH-DPAT and low doses of tropisetron release behaviour suppressed by the aversive situation.	8-Hydroxy-2-(di-n-propylamino)tetralin	216-225	5-hydroxytryptamine receptor 3A	Rattus norvegicus	193-207