PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
30772128-4	2019	Furthermore, selected compounds 3, 8, 9, 19 and 21 with spatial distances between the next carbon to Dpa and the next carbon to cyclam within the range of 6.5-7.5 A showed potent binding affinity selective for CXCR4 with IC50 values of 1.6, 7.9, 5.7, 3.5 and 4.5 nM, respectively, with corresponding high anti-HIV activity with EC50s of 28, 13, 21, 28 and 61 nM, respectively, in the presence of zinc (II) ion.	2,2'-dipicolylamine	101-104	C-X-C motif chemokine receptor 4	Homo sapiens	210-215	
23086703-1	2013	Low-molecular-weight CXCR4 ligands based on known lead compounds including the 14-mer peptide T140, the cyclic pentapeptide FC131, peptide mimetics, and dipicolylamine-containing compounds were designed and synthesized.	2,2'-dipicolylamine	153-167	C-X-C motif chemokine receptor 4	Homo sapiens	21-26	
16722661-0	2006	Identification of a new class of low molecular weight antagonists against the chemokine receptor CXCR4 having the dipicolylamine-zinc(II) complex structure.	2,2'-dipicolylamine	114-128	C-X-C motif chemokine receptor 4	Homo sapiens	97-102