PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
22794275-1	2012	Tetrahydroquinolines (THQs), a new class of nonsteroidal selective androgen receptor (AR) modulators, have two indispensable functional groups, that is, a hydroxyl group for AR binding and a nitro group for agonistic activity.	nitro	191-196	androgen receptor	Homo sapiens	86-88	
31267866-3	2019	Pharmacophore-based studies revealed that the nitro- or cyano-substituted anilide groups have influenced the activity profiles of non-steroidal AR antagonists, followed by the molecular docking studies with five AR receptors.	nitro	46-51	androgen receptor	Homo sapiens	144-146	
24900588-3	2013	Structure-activity relationship studies confirmed that the pharmacophore of these novel AR antagonists is distinct from the nitro- or cyano-substituted anilide substructure of other nonsteroidal AR antagonists.	nitro	124-129	androgen receptor	Homo sapiens	88-90	
19022677-5	2009	The results suggest that this heterocyclic functionality is potential bioisoster of the nitro and cyano groups forming the polar pharmacophores of known non-steroidal AR ligands.	nitro	88-93	androgen receptor	Homo sapiens	167-169