PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
29955703-13	2017	GEN and flavone antagonists of AhR may be useful for reactivation of BRCA1 and ERalpha via CpG demethylation in ERalpha-negative breast cancer cells harboring constitutively active AhR.	flavone	8-15	estrogen receptor 1	Homo sapiens	79-86	
29955703-13	2017	GEN and flavone antagonists of AhR may be useful for reactivation of BRCA1 and ERalpha via CpG demethylation in ERalpha-negative breast cancer cells harboring constitutively active AhR.	flavone	8-15	estrogen receptor 1	Homo sapiens	112-119	
22634477-5	2012	In MCF-7 breast carcinoma cells chalcone and flavone suppress ERalpha activity through stimulation of the stress-activated members of the mitogen-activated protein kinase (MAPK) family: c-Jun N-terminal kinase (JNK)1 and JNK2.	flavone	45-52	estrogen receptor 1	Homo sapiens	62-69	
17379515-0	2007	Synthesis, characterization, and estrogen receptor binding affinity of flavone-, indole-, and furan-estradiol conjugates.	flavone	71-78	estrogen receptor 1	Homo sapiens	33-50	
17379515-3	2007	In vitro competitive binding assays for the estrogen receptor (alpha-ER), using [(3)H]estradiol (RBA=100) as a competitor, revealed that a two-carbon alkyl linker combined with a flavone conjugate provided the highest binding affinity (RBA approximately 9), warranting further studies on their potential use as selective estrogen-receptor modulators (SERMs) for hormone-replacement therapies.	flavone	179-186	estrogen receptor 1	Homo sapiens	44-61