PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
2436829-14	1987	Distinct receptors for verapamil and diltiazem are poorly defined, but appear to be allosterically related to the dihydropyridine receptor.	Diltiazem	37-46	calcium voltage-gated channel subunit alpha1 S	Homo sapiens	114-138	
9514900-3	1998	In both cardiac SLM and SR, the felodipine fluorescence was sensitive to conformational changes of the DHPR, as diltiazem that binds to DHPR at a separate site altered the values of both the Kd and the Hill coefficient characteristic for felodipine binding.	Diltiazem	112-121	calcium voltage-gated channel subunit alpha1 S	Homo sapiens	103-107	
9514900-3	1998	In both cardiac SLM and SR, the felodipine fluorescence was sensitive to conformational changes of the DHPR, as diltiazem that binds to DHPR at a separate site altered the values of both the Kd and the Hill coefficient characteristic for felodipine binding.	Diltiazem	112-121	calcium voltage-gated channel subunit alpha1 S	Homo sapiens	136-140	
12037132-13	2002	We confirmed that Ca(2+) enters the cells through the dihydropyridine receptor (DHPR, also known as the L-channel) by demonstrating inhibition by diltiazem.	Diltiazem	146-155	calcium voltage-gated channel subunit alpha1 S	Homo sapiens	54-78	
31150622-2	2019	Here, we report the cryoelectron microscopy (cryo-EM) structures of Cav1.1 in complex with archetypal antagonistic drugs, nifedipine, diltiazem, and verapamil, at resolutions of 2.9 A, 3.0 A, and 2.7 A, respectively, and with a DHP agonist Bay K 8644 at 2.8 A.	Diltiazem	134-143	calcium voltage-gated channel subunit alpha1 S	Homo sapiens	68-74