PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
30556625-3	2019	The crown-ether complexes of sodium (1-Na) and potassium (1-K) exhibited different structures, with sodium preferring coordination to the nitrogen end, whereas potassium binds in an unusual eta2 -coordination mode to the two central carbon atoms.	1-na	37-41	DNA polymerase iota	Homo sapiens	190-194
30822441-5	2019	In the present work, we have used 1-Naphthyl acetate (1-NA) as a fluorogenic substrate for the estimation of AChE activity of human erythrocytes.	1-na	54-58	acetylcholinesterase (Cartwright blood group)	Homo sapiens	109-113
30822441-7	2019	Therefore, using 1-NA, we have developed a rapid, sensitive and baseline free assay for the estimation of AChE activity.	1-na	17-21	acetylcholinesterase (Cartwright blood group)	Homo sapiens	106-110
8055632-6	1994	(ii) With cell-expressed rat UGT1.6, non-carcinogenic 1-NA was conjugated with the highest rate and with higher affinity than 2-NA.	1-na	54-58	UDP glucuronosyltransferase family 1 member A6	Rattus norvegicus	29-35
30201403-7	2018	Among the screened substrates, 1-Naphthyl acetate (1-NA) exhibited the most favorable interaction with AChE in terms of highest TIE and corresponding high Goldscore.	1-na	51-55	acetylcholinesterase (Cartwright blood group)	Homo sapiens	103-107
30201403-10	2018	We observed 1-NA to be a better alternative substrate for AChE than ATCh in terms of lower Km value.	1-na	12-16	acetylcholinesterase (Cartwright blood group)	Homo sapiens	58-62
30201403-12	2018	Therefore, we propose that 1-NA can be an attractive chromogenic substrate for the measurement of AChE activity, and it possess the potential to detect organophosphorus pesticide (OP) poisoning.	1-na	27-31	acetylcholinesterase (Cartwright blood group)	Homo sapiens	98-102
30155206-7	2017	The reaction between 1-Na and S8 affords an insoluble, presumably polymeric paramagnetic complex with bridging uranium sulfides, while that with CS2 results in oxidation of each UIII to the notably high UV oxidation state, forming the unusual trithiocarbonate (CS3)2- as a ligand in [{U(CS3)}2(mu-kappa2:kappa2-CS3)(LA)] (4).	1-na	21-25	chorionic somatomammotropin hormone 2	Homo sapiens	145-148
30155206-7	2017	The reaction between 1-Na and S8 affords an insoluble, presumably polymeric paramagnetic complex with bridging uranium sulfides, while that with CS2 results in oxidation of each UIII to the notably high UV oxidation state, forming the unusual trithiocarbonate (CS3)2- as a ligand in [{U(CS3)}2(mu-kappa2:kappa2-CS3)(LA)] (4).	1-na	21-25	myozenin 3	Homo sapiens	261-264
30155206-7	2017	The reaction between 1-Na and S8 affords an insoluble, presumably polymeric paramagnetic complex with bridging uranium sulfides, while that with CS2 results in oxidation of each UIII to the notably high UV oxidation state, forming the unusual trithiocarbonate (CS3)2- as a ligand in [{U(CS3)}2(mu-kappa2:kappa2-CS3)(LA)] (4).	1-na	21-25	myozenin 3	Homo sapiens	287-290
30155206-7	2017	The reaction between 1-Na and S8 affords an insoluble, presumably polymeric paramagnetic complex with bridging uranium sulfides, while that with CS2 results in oxidation of each UIII to the notably high UV oxidation state, forming the unusual trithiocarbonate (CS3)2- as a ligand in [{U(CS3)}2(mu-kappa2:kappa2-CS3)(LA)] (4).	1-na	21-25	myozenin 3	Homo sapiens	287-290
8055632-8	1994	(iii) Substrate specificity of human UGT1.6 also appeared to be limited to planar 1-NA, 2-NA and its N-hydroxy derivative, whereas UGT1.7 showed broader substrate specificity, including the bulky arylamine 4-ABP and its N-hydroxy derivative.	1-na	82-86	UDP glucuronosyltransferase family 1 member A6	Homo sapiens	37-43