PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
19066725-5	2009	From the SAR studies, it reveals that, the substitution at N-terminal of 6-fluoro-3-(4-piperidinyl)-1,2-benzisoxazole by the heterocyclic ring plays a dominant role and was responsible for the antiproliferative activity.	3-(4-piperidyl)-6-fluoro-1,2-benzisoxazole	73-117	sarcosine dehydrogenase	Homo sapiens	9-12
21211872-1	2011	The peptides of elastin sequences chosen for the present study included tetrapeptides, pentapeptides and tricosapeptides (30 amino acids), synthesized by classical solution phase method and conjugated to [3-(4-piperidyl)-6-fluoro-1,2-benzisoxazole].	3-(4-piperidyl)-6-fluoro-1,2-benzisoxazole	205-247	elastin	Homo sapiens	16-23