PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
23906970-4	2013	Twenty four-hour incubation of cells with antidepressants (0.05-10 muM) and DEX (10 muM) showed that imipramine, amitriptyline, desipramine, citalopram and fluoxetine at concentrations from 0.1 up to 1 muM, reboxetine (0.1 muM) and tianeptine (0.05 muM) prevented the DEX-induced decreases in cell viability and proliferation rate.	Imipramine	101-111	latexin	Homo sapiens	67-70	
32240535-5	2020	METHODS: SH-SY5Y cells were preincubated with mirtazapine and imipramine (1-20 muM) for 24 h, then hydrogen peroxide (H2O2) was added into the medium containing the antidepressants for additional 24 h, and MTT assay was carried out subsequently.	Imipramine	62-72	latexin	Homo sapiens	79-82	
32240535-6	2020	Also, to elucidate the molecular mechanism underlying the neuroprotective properties of antidepressants, we investigated the effects of mirtazapine and imipramine (2 muM) in pro- and anti-apoptotic proteins gene expression in SH-SY5Y cells.	Imipramine	152-162	latexin	Homo sapiens	166-169	
20654293-4	1997	Optimal concentrations for the formation of these structures were 20 muM for clomipramine and 40 muM for imipramine.	Imipramine	105-115	latexin	Homo sapiens	97-100	
5015032-15	1972	Methysergide was a weak inhibitor of 5-HT uptake (K(i) approximately 125 muM) whereas imipramine was very effective (K(i) approximately 0.3 muM).10.	Imipramine	86-96	latexin	Homo sapiens	140-143	
23906970-4	2013	Twenty four-hour incubation of cells with antidepressants (0.05-10 muM) and DEX (10 muM) showed that imipramine, amitriptyline, desipramine, citalopram and fluoxetine at concentrations from 0.1 up to 1 muM, reboxetine (0.1 muM) and tianeptine (0.05 muM) prevented the DEX-induced decreases in cell viability and proliferation rate.	Imipramine	101-111	latexin	Homo sapiens	84-87	
23906970-4	2013	Twenty four-hour incubation of cells with antidepressants (0.05-10 muM) and DEX (10 muM) showed that imipramine, amitriptyline, desipramine, citalopram and fluoxetine at concentrations from 0.1 up to 1 muM, reboxetine (0.1 muM) and tianeptine (0.05 muM) prevented the DEX-induced decreases in cell viability and proliferation rate.	Imipramine	101-111	latexin	Homo sapiens	84-87	
23906970-4	2013	Twenty four-hour incubation of cells with antidepressants (0.05-10 muM) and DEX (10 muM) showed that imipramine, amitriptyline, desipramine, citalopram and fluoxetine at concentrations from 0.1 up to 1 muM, reboxetine (0.1 muM) and tianeptine (0.05 muM) prevented the DEX-induced decreases in cell viability and proliferation rate.	Imipramine	101-111	latexin	Homo sapiens	84-87	
23906970-4	2013	Twenty four-hour incubation of cells with antidepressants (0.05-10 muM) and DEX (10 muM) showed that imipramine, amitriptyline, desipramine, citalopram and fluoxetine at concentrations from 0.1 up to 1 muM, reboxetine (0.1 muM) and tianeptine (0.05 muM) prevented the DEX-induced decreases in cell viability and proliferation rate.	Imipramine	101-111	latexin	Homo sapiens	84-87	
21961110-4	2011	A good linear correlation is observed for the dependence of the SERS signal at 684 cm(-1) (R(2) = 0.9997) on Imi concentration over the range of 0.75-7.5 muM.	Imipramine	109-112	latexin	Homo sapiens	154-157	
21961110-5	2011	The limit of detection of imipramine in the silver colloidal solution is 0.98 muM.	Imipramine	26-36	latexin	Homo sapiens	78-81	
21697722-7	2011	Verapamil, carvedilol, imipramine, and cimetidine were competitive inhibitors of OCT3-mediated metformin uptake (Ki 3.6-15.8 muM).	Imipramine	23-33	latexin	Homo sapiens	125-128	
21273663-4	2010	Imipramine moderately diminished the rate of chlorpromazine 5-sulfoxidation (K(i) = 8.7 muM, competitive inhibition), mono-N-demethylation (K(i) = 16.0 muM, non-competitive inhibition) and di-N-demethylation (K(i) = 13.5 muM mixed inhibition).	Imipramine	0-10	latexin	Homo sapiens	88-91	
21273663-4	2010	Imipramine moderately diminished the rate of chlorpromazine 5-sulfoxidation (K(i) = 8.7 muM, competitive inhibition), mono-N-demethylation (K(i) = 16.0 muM, non-competitive inhibition) and di-N-demethylation (K(i) = 13.5 muM mixed inhibition).	Imipramine	0-10	latexin	Homo sapiens	152-155	
21273663-4	2010	Imipramine moderately diminished the rate of chlorpromazine 5-sulfoxidation (K(i) = 8.7 muM, competitive inhibition), mono-N-demethylation (K(i) = 16.0 muM, non-competitive inhibition) and di-N-demethylation (K(i) = 13.5 muM mixed inhibition).	Imipramine	0-10	latexin	Homo sapiens	152-155