PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
35453603-2	2022	To this end, the cytotoxic potential of raloxifene and the synthetic curcumin derivative 2,6-bis (pyridin-4-ylmethylene)-cyclohexanone (RL91) was examined in AR-(PC3 and DU145) cells and AR+ (LnCaP) CRPC cells.	Raloxifene Hydrochloride	40-50	androgen receptor	Homo sapiens	158-160	
35453603-2	2022	To this end, the cytotoxic potential of raloxifene and the synthetic curcumin derivative 2,6-bis (pyridin-4-ylmethylene)-cyclohexanone (RL91) was examined in AR-(PC3 and DU145) cells and AR+ (LnCaP) CRPC cells.	Raloxifene Hydrochloride	40-50	androgen receptor	Homo sapiens	187-189	
16604181-3	2003	The discovery of raloxifene and other selective estrogen receptor modulators (SERMs) has raised the possibility of generating selective compounds for other pathways, including androgens (that is, selective androgen receptor modulators, or SARMs).	Raloxifene Hydrochloride	17-27	androgen receptor	Homo sapiens	206-223	
3402389-4	1988	Mediation of the action of E2 by the androgen receptor is indicated by the absence of interference of E2 action by the antiestrogen LY156758 while the antiandrogen hydroxyflutamide (3 microM) caused a 50% inhibition of E2 action.	Raloxifene Hydrochloride	132-140	androgen receptor	Homo sapiens	37-54