PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
23292320-2	2013	The formation of these azole:BeXH(BeX2) complexes is accompanied by a dramatic enhancement of the intrinsic acidity of the azole, as the deprotonated azole is much more stable after the aforementioned interaction.	Azoles	123-128	brain expressed X-linked 2	Homo sapiens	34-38	
23292320-2	2013	The formation of these azole:BeXH(BeX2) complexes is accompanied by a dramatic enhancement of the intrinsic acidity of the azole, as the deprotonated azole is much more stable after the aforementioned interaction.	Azoles	123-128	brain expressed X-linked 2	Homo sapiens	34-38	
23292320-3	2013	Most importantly, the increase in acidity is so large that the azole:BeXH or azole:BeX2 complexes behave as NH acids, which are stronger than typical oxyacids such as phosphoric acid and oxalic acid.	Azoles	77-82	brain expressed X-linked 2	Homo sapiens	83-87	
23873588-2	2013	The association of BeX2 (X: H, F, Cl) derivatives with azoles leads to a dramatic increase of their intrinsic acidity.	Azoles	55-61	brain expressed X-linked 2	Homo sapiens	19-23	
23292320-2	2013	The formation of these azole:BeXH(BeX2) complexes is accompanied by a dramatic enhancement of the intrinsic acidity of the azole, as the deprotonated azole is much more stable after the aforementioned interaction.	Azoles	23-28	brain expressed X-linked 2	Homo sapiens	34-38