PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
29960729-3	2018	This prompted us to design and synthesize azole-based H3R ligands, i.e. having oxadiazole- or thiazole-based core structures.	Azoles	42-47	histamine receptor H3	Homo sapiens	54-57	
20727744-0	2010	Azole derivatives as histamine H3 receptor antagonists, part 2: C-C and C-S coupled heterocycles.	Azoles	0-5	histamine receptor H3	Homo sapiens	21-42	
20727744-1	2010	With a small series of compounds we demonstrated the variability in the core region of the human histamine H(3) receptor (hH(3)R) antagonist structural blueprint by introducing polar azole groups (oxazole, oxadiazole, thiazole and triazole).	Azoles	183-188	histamine receptor H3	Homo sapiens	97-120	
20727744-1	2010	With a small series of compounds we demonstrated the variability in the core region of the human histamine H(3) receptor (hH(3)R) antagonist structural blueprint by introducing polar azole groups (oxazole, oxadiazole, thiazole and triazole).	Azoles	183-188	histamine receptor H3	Homo sapiens	122-128	
20728354-0	2010	Azole derivatives as histamine H3 receptor antagonists, part I: thiazol-2-yl ethers.	Azoles	0-5	histamine receptor H3	Homo sapiens	21-42