PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
35512065-5	2022	METHODS: In this study, for the first time, compound 5 possessing a novel salicylamide zinc-binding group was synthesized and evaluated biologically for its ability to inhibit various HDAC isoforms and induce acetylation upon alpha-tubulin and histone H3 among MDA-MB-231 cells.	salicylamide	74-86	tubulin alpha 1b	Homo sapiens	226-239	
35512065-8	2022	Moreover, the molecular docking study indicated that the salicylamide zinc-binding group of compound 5 coordinates the active zinc ion of class I HDAC2 in a bidentate fashion.	salicylamide	57-69	histone deacetylase 2	Homo sapiens	146-151