PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
21489792-6	2011	In particular, compound 17 with the aromatic piperazinosulfonyl substituent showed the most potent (IC(50)=1.30 muM) and selective (over other kinases such as p38alpha, p38beta, JNK1, JNK2, JNK3, and IKK-1) inhibitory activity against IKK-2.	aromatic piperazinosulfonyl	36-63	latexin	Homo sapiens	112-115