PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
13826989-0	1960	Competitive inhibition of acetylcholinesterase by several thiazolines and oxazolines.	oxazolines	74-84	acetylcholinesterase (Cartwright blood group)	Homo sapiens	26-46
28885838-2	2017	The addition of nitriles on these intermediates occurred with high to excellent syn diastereoselectivity and led, in most cases, to oxazolines and amides as single diastereomers.	oxazolines	132-142	synemin	Homo sapiens	80-83
24910245-0	2014	Design and synthesis of D-ring steroidal isoxazolines and oxazolines as potential antiproliferative agents against LNCaP, PC-3 and DU-145 cells.	oxazolines	43-53	chromobox 8	Homo sapiens	122-126
13678192-1	2003	Potassium alkoxides of N-acyloxazolidin-2-one derived syn-aldolates undergo a novel tandem intramolecular cyclisation elimination reaction to afford trisubstituted (E)-alpha,beta-unsaturated amides in high d.e., which may be converted into their corresponding acids or oxazolines in good yield.	oxazolines	269-279	synemin	Homo sapiens	54-57
26605701-0	2015	Palladium-Catalyzed C-2 C-H Heteroarylation of Chiral Oxazolines: Diverse Synthesis of Chiral Oxazoline Ligands.	oxazolines	54-64	complement C2	Homo sapiens	20-23
25941908-3	2015	Oxazolines syn-2 were transformed to C-quaternary threoninol, threoninal, and threonine derivatives which can be further incorporated into complex natural compounds.	oxazolines	0-10	synapsin II	Homo sapiens	11-16
25699577-1	2015	A highly enantioselective bromocyclization of allylic amides with N-bromosuccinimide (NBS) was developed with DTBM-BINAP as a catalyst, affording chiral oxazolines with a tetrasubstituted carbon center in high yield with up to 99% ee.	oxazolines	153-163	nibrin	Homo sapiens	86-89
18459808-1	2008	Treatment of alkenes with NBS, a nitrile, NaHCO3 and water in the presence of Cu(OTf)2 or Zn(OTf)2 is reported to furnish oxazolines in one pot and good yields.	oxazolines	122-132	nibrin	Homo sapiens	26-29
18459808-1	2008	Treatment of alkenes with NBS, a nitrile, NaHCO3 and water in the presence of Cu(OTf)2 or Zn(OTf)2 is reported to furnish oxazolines in one pot and good yields.	oxazolines	122-132	POU class 2 homeobox 2	Homo sapiens	78-86
11667808-4	1996	The main limitation of this method was shown when the oxidation failed with oxazolines/thiazolines lacking the carboalkoxy group at C-4.	oxazolines	76-86	complement C4A (Rodgers blood group)	Homo sapiens	132-135