PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
23330926-8	2013	3) For isoflavones, the microsomal hydroxylation is observed at the C-3"-, C-6 and C-8- position when there is a single or no hydroxy group on the B-ring.	Isoflavones	7-18	complement C3	Homo sapiens	68-71	
31621310-7	2019	These results coupled with simulation studies modeling flavonoid interaction within the AhR binding pocket demonstrate that the orientation of the substituted phenyl ring at C-2 (flavones) or C-3 (isoflavones) on the common 4-H-chromen-4-one ring strongly influences the activities of isoflavones and flavones as AhR agonists.	Isoflavones	197-208	complement C3	Homo sapiens	192-195	
31621310-7	2019	These results coupled with simulation studies modeling flavonoid interaction within the AhR binding pocket demonstrate that the orientation of the substituted phenyl ring at C-2 (flavones) or C-3 (isoflavones) on the common 4-H-chromen-4-one ring strongly influences the activities of isoflavones and flavones as AhR agonists.	Isoflavones	285-296	complement C3	Homo sapiens	192-195	
22292767-4	2012	The hydroxylation on A-ring of flavones and isoflavones, especially at C-5 and C-7, significantly enhanced the inhibitory activities against digestive enzymes and the hydroxylation on positions C-3" and C-4" of B-ring of flavonoids remarkably improved the inhibition.	Isoflavones	44-55	complement C3	Homo sapiens	194-197