Compounds > fpl 64176

fpl 64176 and isradipine

fpl 64176 has been researched along with isradipine in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's4 (80.00)18.2507
2000's1 (20.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Lacerda, AE; Rampe, D1
Rampe, D; Triggle, DJ; Zheng, W1
Dooley, DJ; Feuerstein, TJ; Ginap, T1
Glossmann, H; Grabner, M; Hering, S; Striessnig, J; Wang, Z1
Adachi-Akahane, S; Ichijo, H; Nagao, T; Yamaguchi, S; Yoshioka, K; Zhorov, BS1

Other Studies

5 other study(ies) available for fpl 64176 and isradipine

ArticleYear
A new site for the activation of cardiac calcium channels defined by the nondihydropyridine FPL 64176.
    The Journal of pharmacology and experimental therapeutics, 1991, Volume: 259, Issue:3

    Topics: Animals; Barium; Calcium; Calcium Channel Blockers; Calcium Channels; Cells, Cultured; Dihydropyridines; Electrophysiology; Heart; Heart Ventricles; Isradipine; Myocardium; Potassium; Pyrroles; Rats; Ventricular Function

1991
Pharmacological, radioligand binding, and electrophysiological characteristics of FPL 64176, a novel nondihydropyridine Ca2+ channel activator, in cardiac and vascular preparations.
    Molecular pharmacology, 1991, Volume: 40, Issue:5

    Topics: 3-Pyridinecarboxylic acid, 1,4-dihydro-2,6-dimethyl-5-nitro-4-(2-(trifluoromethyl)phenyl)-, Methyl ester; Animals; Calcium Channel Blockers; Calcium Channels; Dihydropyridines; Diltiazem; Dose-Response Relationship, Drug; Heart; In Vitro Techniques; Isradipine; Male; Myocardium; Potassium; Pyrroles; Radioligand Assay; Rats; Vasoconstriction; Verapamil

1991
The non-dihydropyridine L-type voltage-sensitive calcium channel activator FPL 64176 enhances K(+)-evoked efflux of [3H]norepinephrine from rat neocortical slices.
    Neuroscience letters, 1993, Jun-25, Volume: 156, Issue:1-2

    Topics: 3-Pyridinecarboxylic acid, 1,4-dihydro-2,6-dimethyl-5-nitro-4-(2-(trifluoromethyl)phenyl)-, Methyl ester; Animals; Binding, Competitive; Calcium Channels; Cell Membrane; Cerebral Cortex; Dose-Response Relationship, Drug; In Vitro Techniques; Isradipine; Kinetics; Male; Norepinephrine; Potassium; Pyrroles; Rats; Rats, Sprague-Dawley; Tritium

1993
Transfer of 1,4-dihydropyridine sensitivity from L-type to class A (BI) calcium channels.
    Neuron, 1996, Volume: 16, Issue:1

    Topics: Amino Acid Sequence; Animals; Binding Sites; Calcium; Calcium Channel Agonists; Calcium Channel Blockers; Calcium Channels; Calcium Channels, L-Type; Carps; Dihydropyridines; Ion Channel Gating; Isradipine; Molecular Sequence Data; omega-Agatoxin IVA; omega-Conotoxins; Peptide Fragments; Peptides; Protein Structure, Tertiary; Pyrroles; Rabbits; Recombinant Fusion Proteins; Sequence Alignment; Sequence Homology, Amino Acid; Spider Venoms

1996
Key roles of Phe1112 and Ser1115 in the pore-forming IIIS5-S6 linker of L-type Ca2+ channel alpha1C subunit (CaV 1.2) in binding of dihydropyridines and action of Ca2+ channel agonists.
    Molecular pharmacology, 2003, Volume: 64, Issue:2

    Topics: Alanine; Animals; Calcium Channel Agonists; Calcium Channel Blockers; Calcium Channels, L-Type; Dihydropyridines; Isradipine; Phenylalanine; Point Mutation; Protein Subunits; Pyrroles; Rats; Repetitive Sequences, Nucleic Acid; Serine

2003