PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
20932608-1	2010	In this work, we report the synthesis and the antitubercular evaluation of 16 new mefloquine derivatives, formed from reactions between mefloquine and benzaldehydes, with the activity expressed as the minimum inhibitory concentration (MIC) in muM.	Mefloquine	82-92	latexin	Homo sapiens	243-246	
28068604-5	2017	We found that quinoline derivatives 3a and 4 were the most potent compounds within this series, both with mean EC50 values of 0.8 muM, which represents a potency 5 times that of mefloquine.	Mefloquine	178-188	latexin	Homo sapiens	130-133