PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
28068548-1	2017	Nitrile groups in the polymer of intrinsic microporosity PIM-1 were modified by base-catalysed hydrolysis, by reaction with ethanolamine and diethanolamine, and by reduction to amine, and the products investigated for their ability to take up a range of dyes from aqueous or ethanolic solution.	Amines	131-136	Pim-1 proto-oncogene, serine/threonine kinase	Homo sapiens	57-62	
31368688-3	2019	The amine-appended PIMs not only showed a nearly four-fold enhancement in CO2 loading capacity (36.4 cc/g at 0.15 bar and 298 K) and very high CO2/N2 selectivity compared to neat PIM-1 but also proved to have stable performance when cycled between adsorption and desorption isotherms under both dry and humid conditions that are typical for postcombustion CO2 capture.	Amines	4-9	Pim-1 proto-oncogene, serine/threonine kinase	Homo sapiens	179-184	
24860196-1	2014	Nitrile groups in the polymer of intrinsic microporosity PIM-1 were reduced to primary amines using borane complexes.	Amines	87-93	Pim-1 proto-oncogene, serine/threonine kinase	Homo sapiens	57-62	
24860196-6	2014	Thus, for the H2/CO2 gas pair, whereas PIM-1 favors CO2, amine-PIM-1 shows permselectivity toward H2, breaking the Robeson 2008 upper bound.	Amines	57-62	Pim-1 proto-oncogene, serine/threonine kinase	Homo sapiens	63-68	
17107048-3	2006	The quenching of this activated ester with a library of primary amines, followed by testing of the resulting amide library, led to the identification of organometallic Pim-1 and GSK-3 inhibitors with improved potencies and kinase selectivities.	Amines	64-70	Pim-1 proto-oncogene, serine/threonine kinase	Homo sapiens	168-173