PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
1655490-3	1991	The potency of most antagonists to inhibit [3H]nitrendipine binding was correlated with their calmodulin inhibitory potency.	[3h]nitrendipine	43-59	calmodulin 1	Rattus norvegicus	94-104
9596559-2	1998	Following exposure to the maximum concentration of PLP (100 mM), [3H]nitrendipine binding was inhibited by up to 96.5%.	[3h]nitrendipine	65-81	myelin proteolipid protein	Oryctolagus cuniculus	51-54
9596559-3	1998	Scatchard analysis of the binding data indicated that treatment with PLP resulted in a loss of [3H]nitrendipine binding sites with no effect on binding affinity.	[3h]nitrendipine	95-111	myelin proteolipid protein	Oryctolagus cuniculus	69-72
8709127-6	1996	Specifically, in rat cortex homogenate, our prototypic PBR ligand 7-acetoxy-6-(p-methoxyphenyl)pyrrolo[2,1-d][1,5]benzothiazepine (3) showed an IC50 equal to 0.13 nM for inhibition of [3H]nitrendipine binding.	[3h]nitrendipine	184-200	translocator protein	Rattus norvegicus	55-58
3449204-7	1987	In vivo administration of o-NCS-DHP (5-25 mg/kg) produced a persistent reduction of [3H]nitrendipine binding in rat brain, gut, and heart characterized as Bmax, but not KD, changes.	[3h]nitrendipine	84-100	dihydropyrimidinase	Rattus norvegicus	32-35
2468847-0	1988	Interaction of calmodulin and calcium antagonists with [3H]diltiazem and [3H]nitrendipine binding sites.	[3h]nitrendipine	73-89	calmodulin 1	Homo sapiens	15-25
6433001-5	1984	The effects of cations and calmodulin antagonists on [3H]nitrendipine binding in smooth and cardiac muscle have been studied further.	[3h]nitrendipine	53-69	calmodulin	Oryctolagus cuniculus	27-37
2939463-6	1986	The enantiomers of SKF 10047 (n-allylormetazocine), dextrorphan, levorphanol and the ion channel toxins histrionicotoxin and pumiliotoxin-B also increased the apparent affinity of [3H]nitrendipine, while several local anesthetics and mu-opiate receptor ligands were without effect.	[3h]nitrendipine	180-196	opioid related nociceptin receptor 1	Rattus norvegicus	234-252
6518370-2	1984	On this line, the present study shows that lead alters the characteristics of [3H]nitrendipine ([ 3H]NDP) binding to rat striatal membranes.	[3h]nitrendipine	78-94	norrin cystine knot growth factor NDP	Rattus norvegicus	101-104
6433001-10	1984	However, calmodulin antagonists were found to inhibit [3H]nitrendipine binding with the order of potency: pimozide greater than less than calmidazolium (R 24571) greater than trifluoperazine greater than chlorpromazine greater than promethazine greater than chlorpromazine sulfoxide, that correlates quite well with the potency of these drugs as inhibitors of calmodulin-dependent processes.	[3h]nitrendipine	54-70	calmodulin	Oryctolagus cuniculus	9-19
6433001-10	1984	However, calmodulin antagonists were found to inhibit [3H]nitrendipine binding with the order of potency: pimozide greater than less than calmidazolium (R 24571) greater than trifluoperazine greater than chlorpromazine greater than promethazine greater than chlorpromazine sulfoxide, that correlates quite well with the potency of these drugs as inhibitors of calmodulin-dependent processes.	[3h]nitrendipine	54-70	calmodulin	Oryctolagus cuniculus	360-370
6433001-11	1984	The results suggest that calmodulin antagonists bind to a protein associated with the [3H]nitrendipine binding site that has a hydrophobic domain similar to that exposed on calmodulin by Ca++, but that this protein is not calmodulin itself.	[3h]nitrendipine	86-102	calmodulin	Oryctolagus cuniculus	25-35
6433001-11	1984	The results suggest that calmodulin antagonists bind to a protein associated with the [3H]nitrendipine binding site that has a hydrophobic domain similar to that exposed on calmodulin by Ca++, but that this protein is not calmodulin itself.	[3h]nitrendipine	86-102	calmodulin	Oryctolagus cuniculus	173-183
6433001-11	1984	The results suggest that calmodulin antagonists bind to a protein associated with the [3H]nitrendipine binding site that has a hydrophobic domain similar to that exposed on calmodulin by Ca++, but that this protein is not calmodulin itself.	[3h]nitrendipine	86-102	calmodulin	Oryctolagus cuniculus	173-183
6865927-1	1983	The calmodulin inhibitors R24571 and trifluoperazine were found to inhibit competitively the binding of [3H]nitrendipine to a 48,000 X g particulate fraction of rat brain with IC50 values of 1.0 and 18.8 microM, respectively.	[3h]nitrendipine	104-120	calmodulin 1	Rattus norvegicus	4-14