PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
3240768-5	1988	MCPP, on the other hand, displaced ligands for 5-HT1, 5-HT1A and 5-HT2 binding sites with similar potencies (Ki values = 25 (3, 67), 23 (14, 40) and 40 (33, 48) nM, respectively).	mecoprop	0-4	5-hydroxytryptamine receptor 1A	Rattus norvegicus	54-60	
1387963-0	1992	Etoperidone, trazodone and MCPP: in vitro and in vivo identification of serotonin 5-HT1A (antagonistic) activity.	mecoprop	27-31	5-hydroxytryptamine receptor 1A	Rattus norvegicus	82-88	
1387963-1	1992	The Ki values for etoperidone, trazodone and MCPP (m-chlorophenylpiperazine dihydrochloride) at 5-HT1A sites (using rat cerebral cortical synaptosomes and [3H]8-OH-DPAT) were determined to be 20.2, 23.6 and 18.9 nM, respectively.	mecoprop	45-49	5-hydroxytryptamine receptor 1A	Rattus norvegicus	96-102	
1387963-7	1992	Taken together, the results suggest a predominant antagonistic activity of etoperidone, trazodone and MCPP at 5-HT1A receptor sites in rat central nervous system.	mecoprop	102-106	5-hydroxytryptamine receptor 1A	Rattus norvegicus	110-116	
2150180-9	1990	Forepaw treading in rats induced by the 5-HT1A-agonist 8-OH-DPAT was attenuated by the 5-HT1C-agonists MK 212 and mCPP.	mecoprop	114-118	5-hydroxytryptamine receptor 1A	Rattus norvegicus	40-46