PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
31509959-7	2019	Calcium release from HEK293T cells stably expressing the T2R4 human bitter taste receptor was significantly (p < 0.05) attenuated by BPAH-AGEs (up to 96%) and BPCH-AGEs (up to 92%) when compared to the BPAH (62%) and BPCH (3%) or quinine (0%).	Quinine	230-237	taste 2 receptor member 4	Homo sapiens	57-61	
21303656-11	2011	The functional assays showed an increase in intracellular calcium levels after the application of exogenous ligands for T2R4, denatonium benzoate and quinine to these cultured cells, suggesting that endogenous T2R4 expressed in these cells is functional.	Quinine	150-157	taste 2 receptor member 4	Homo sapiens	210-214	
32413538-3	2020	For examples, amino acid derivatives such as gamma-aminobutyric acid (GABA) and Nalpha,Nalpha-bis(carboxymethyl)-L-Lysine (BCML) blocked responses to quinine mediated by human TAS2R4.	Quinine	150-157	taste 2 receptor member 4	Homo sapiens	176-182	
27288892-9	2016	Interestingly, cholesterol sensitivity of T2R4 was observed at quinine concentrations in the lower mM range.	Quinine	63-70	taste 2 receptor member 4	Homo sapiens	42-46	
25036266-7	2014	Chloroquine, denatonium, dextromethorphan, noscapine and quinine, agonists for TAS2R3, TAS2R4, TAS2R10 and TAS2R14, induced strong endothelium-independent relaxations (responses between 82-96% of maximal relaxations) in phenylephrine pre-contracted guinea-pig aorta that persisted in the presence of L-type Ca2+ and KCa1.1-channel blockers.	Quinine	57-64	taste 2 receptor member 4	Homo sapiens	87-93	
22794107-5	2012	Although the feeding preference varied considerably among different strains and individuals, statistical analysis using large numbers of transformants indicated that transformants expressing T2R4 showed a small but significant increase in the preference for denatonium and quinine, the T2R4 ligands, as compared to the control flies, whereas transformants expressing T2R38 did not.	Quinine	273-280	taste 2 receptor member 4	Homo sapiens	191-195