PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
12652942-1	2003	The paper presents the results of studies of the amounts of diene conjugates, malonic dialdehyde, and Schiff"s bases, which are molecular LPO products in the tissues of the lung, liver, kidney in animals exposed to 4-hour inhalation of cyclic hydrocarbons (pyromellitic dianhydride, durol, pseudocumene, and dioxane-1,4).	schiff"s bases	102-116	lactoperoxidase	Homo sapiens	138-141
19796939-0	2009	Carbonic anhydrase II-induced selection of inhibitors from a dynamic combinatorial library of Schiff"s bases.	schiff"s bases	94-108	carbonic anhydrase 2	Homo sapiens	0-21
16037312-3	2005	In this study we provide the first evidence that this FN3K-dependent deglycation, acting on the Amadori products, is complemented by another deglycation process operating on the very first product of nonenzymatic glycation, glucosylamines (Schiff"s bases).	schiff"s bases	240-254	fructosamine 3 kinase	Homo sapiens	54-58
15499998-3	2004	The Schiff"s bases behaved as medium potency CA I and CA II inhibitors, whereas their metal complexes showed a highly enhanced potency, with several low nanomolar CA II inhibitors detected.	schiff"s bases	4-18	carbonic anhydrase 1	Homo sapiens	45-49
15499998-3	2004	The Schiff"s bases behaved as medium potency CA I and CA II inhibitors, whereas their metal complexes showed a highly enhanced potency, with several low nanomolar CA II inhibitors detected.	schiff"s bases	4-18	carbonic anhydrase 2	Homo sapiens	54-59
15499998-3	2004	The Schiff"s bases behaved as medium potency CA I and CA II inhibitors, whereas their metal complexes showed a highly enhanced potency, with several low nanomolar CA II inhibitors detected.	schiff"s bases	4-18	carbonic anhydrase 2	Homo sapiens	163-168
34553298-0	2022	Discovery, synthesis and in combo studies of Schiff"s bases as promising dipeptidyl peptidase-IV inhibitors.	schiff"s bases	45-59	dipeptidylpeptidase 4	Mus musculus	73-96
687573-6	1978	The conformation of the N--Calpha bond was found to be approximately the same for all the Schiff"s bases studied based on the long-range coupling constants 3J(C4"--Halpha) of these compounds, and the NOE studies indicate that there is a close spatial relationship between H4" and Halpha.	schiff"s bases	90-104	CEA cell adhesion molecule 6	Homo sapiens	24-33
30644339-2	2018	RESULTS: Accumulation of the DNA damage (8HOdG) products and the end products of LPO (including aldehyde, diene, triene conjugates and Schiff"s bases) were noted in the research studies.	schiff"s bases	135-149	lactoperoxidase	Homo sapiens	81-84