PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
10598624-8	1999	The expression of c-Fos induced by potassium chloride was also suppressed by dibucaine, tetracaine (concentrations that inhibited 50% of the activity of positive control [IC50s] were 16.2+/-0.2 and 73.2+/-0.7 microM, respectively), and PD 98059, a mitogen-activated/extracellular receptor-regulated kinase inhibitor.	Tetracaine	88-98	Fos proto-oncogene, AP-1 transcription factor subunit	Rattus norvegicus	18-23	
10598624-11	1999	CONCLUSIONS: Dibucaine and tetracaine at clinical concentrations were found to inhibit the activation of MAP kinase and the expression of c-Fos mediated by L-type Ca2+ channels in PC12 cells.	Tetracaine	27-37	Fos proto-oncogene, AP-1 transcription factor subunit	Rattus norvegicus	138-143