PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
29232839-6	2017	However, the sedative-hypnotic effects were blocked by the type A GABA (GABAA) receptor antagonists bicuculline and flumazenil.	Flumazenil	116-126	gamma-aminobutyric acid (GABA) A receptor, subunit gamma 1	Mus musculus	72-77	
2554616-5	1989	Systemic flumazepil administration contributed to the memory trace reproduction against the background of GABA-A receptors activation by muscimol in the dose of 0.5 mg/kg.	Flumazenil	9-19	gamma-aminobutyric acid (GABA) A receptor, subunit gamma 1	Mus musculus	106-112	
33143464-4	2021	The effect of selective receptor antagonist GABAA on anticonvulsant activity was investigated with flumazenil.	Flumazenil	99-109	gamma-aminobutyric acid (GABA) A receptor, subunit gamma 1	Mus musculus	44-49	
28551554-7	2017	Ketanserin (6mug), a 5-HT2A/C receptor antagonist, and flumazenil (6mug), a GABAA receptor antagonist, abolished the antihyperalgesic effect of mexicanolide 1 (3mug).	Flumazenil	55-65	gamma-aminobutyric acid (GABA) A receptor, subunit gamma 1	Mus musculus	76-81	
23806621-10	2013	The GABAA inverse agonist, FG-7142, reduced sociability and this was reversed by the GABAA antagonist, flumazenil and dcycloserine, but not by clozapine, or the GABAA benzodiazepine anxiolytic, alprazolam.	Flumazenil	103-113	gamma-aminobutyric acid (GABA) A receptor, subunit gamma 1	Mus musculus	4-9	
28111292-4	2017	Midazolam-induced p-MEK1/2 upregulation was prevented by pretreatment (30min) with flumazenil (10mg/kg), indicating the involvement of GABAA receptors.	Flumazenil	83-93	gamma-aminobutyric acid (GABA) A receptor, subunit gamma 1	Mus musculus	135-140	
27573669-9	2016	These effects of (-)-alpha-pinene on sleep and inhibitory synaptic response were mimicked by zolpidem, acting as a modulator for GABAA-BZD receptors, and fully antagonized by flumazenil, an antagonist for GABAA-BZD receptor.	Flumazenil	175-185	gamma-aminobutyric acid (GABA) A receptor, subunit gamma 1	Mus musculus	205-210	
21518336-6	2011	The anti-epileptic effect of magnolol was reversed by the GABA(A)/benzodiazepine receptor antagonist flumazenil.	Flumazenil	101-111	gamma-aminobutyric acid (GABA) A receptor, subunit gamma 1	Mus musculus	58-89	
11669460-6	2001	TJ-24-induced SI behavior was significantly blocked by the GABA(A)/BZP receptor inverse agonist Ro 15-4513 and the GABA(A)/BZP receptor antagonist flumazenil.	Flumazenil	147-157	gamma-aminobutyric acid (GABA) A receptor, subunit gamma 1	Mus musculus	115-135	
17570441-8	2007	In addition, the anxiolytic-like properties of sinapic acid examined in the EPM test were blocked by flumazenil or bicuculline, which are GABA(A) antagonists.	Flumazenil	101-111	gamma-aminobutyric acid (GABA) A receptor, subunit gamma 1	Mus musculus	138-145	
21945440-5	2011	The hypnotic activity of ILTG was fully inhibited by flumazenil (FLU), a specific gamma-aminobutyric acid type A (GABA(A))-benzodiazepine (BZD) receptor antagonist.	Flumazenil	53-63	gamma-aminobutyric acid (GABA) A receptor, subunit gamma 1	Mus musculus	114-152	
21945440-5	2011	The hypnotic activity of ILTG was fully inhibited by flumazenil (FLU), a specific gamma-aminobutyric acid type A (GABA(A))-benzodiazepine (BZD) receptor antagonist.	Flumazenil	65-68	gamma-aminobutyric acid (GABA) A receptor, subunit gamma 1	Mus musculus	114-152	
15582681-13	2004	The inhibition of U50 tolerance by melatonin was reversed by the chronic treatment with flumazenil (0.1 mg/kg), a benzodiazepine receptor antagonist and picrotoxin (1 mg/kg), a GABAA-gated chloride channel blocker.	Flumazenil	88-98	gamma-aminobutyric acid (GABA) A receptor, subunit gamma 1	Mus musculus	177-182	
8972548-4	1996	In contrast, progesterone (1 mg/kg, for 9 days) produced a significant antistress effect, which was blocked by GABA-A antagonists picrotoxin (1 mg/kg) and bicuculline (1 mg/kg), but not by flumazenil (2 mg/kg), a specific benzodiazepine (BZD) antagonist.	Flumazenil	189-199	gamma-aminobutyric acid (GABA) A receptor, subunit gamma 1	Mus musculus	111-117