PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
26227779-2	2015	N-(4-Chlorophenyl)-2-(piperazin-1-yl)quinazolin-4-amine (5o) has a Ki value of 14.04 +- 0.21 nM, with a selectivity more than 10,000 fold over 5-HT1A receptors (D1 and D2-like receptors).	5o	57-59	5-hydroxytryptamine receptor 1A	Homo sapiens	143-149
35436756-9	2022	5o induces cell apoptosis in a dose-dependent manner through PI3K/Akt/FoxO1 and NF-kappaB signaling pathways.	5o	0-2	AKT serine/threonine kinase 1	Homo sapiens	66-69
35436756-9	2022	5o induces cell apoptosis in a dose-dependent manner through PI3K/Akt/FoxO1 and NF-kappaB signaling pathways.	5o	0-2	forkhead box O1	Homo sapiens	70-75
35436756-13	2022	This study reveals that 5o is a promising therapeutic agent against CRC as a novel GRP94 inhibition.	5o	24-26	heat shock protein 90 beta family member 1	Homo sapiens	83-88