d 888 has been researched along with gallopamil in 9 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 2 (22.22) | 18.7374 |
1990's | 3 (33.33) | 18.2507 |
2000's | 4 (44.44) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Dietel, M; Höllt, V; Kouba, M; Vogt, G | 1 |
Van Dyke, K; Ye, ZG | 1 |
van Amsterdam, FT; Zaagsma, J | 1 |
Nawrath, H; Wegener, JW | 2 |
Dierkes, PW; Hochstrate, P; Schlue, WR; Wende, V | 1 |
Hoda, JC; Huber, IG; Sinnegger-Brauns, MJ; Striessnig, J; Walter-Bastl, D; Wappl-Kornherr, E | 1 |
Awasthi, A; Yadav, A | 1 |
Cheng, RCK; Tikhonov, DB; Zhorov, BS | 1 |
9 other study(ies) available for d 888 and gallopamil
Article | Year |
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Stereoisomers of calcium antagonists which differ markedly in their potencies as calcium blockers are equally effective in modulating drug transport by P-glycoprotein.
Topics: Animals; ATP Binding Cassette Transporter, Subfamily B, Member 1; Binding, Competitive; Biological Transport; Calcium Channel Blockers; Cell Line; Dihydropyridines; Drug Resistance; Haplorhini; Immunoblotting; Membrane Glycoproteins; Mice; RNA, Messenger; Stereoisomerism; Verapamil; Vinblastine | 1992 |
Reversal of chloroquine resistance in falciparum malaria independent of calcium channels.
Topics: Animals; Calcium; Chloroquine; Drug Interactions; Drug Resistance; Gallopamil; Ion Channels; Malaria; Plasmodium falciparum; Verapamil | 1988 |
Stereoisomers of calcium antagonists discriminate between coronary vascular and myocardial sites.
Topics: Animals; Bepridil; Calcium Channel Blockers; Coronary Vessels; Gallopamil; Heart; In Vitro Techniques; Male; Pyrrolidines; Rats; Stereoisomerism; Verapamil | 1988 |
Extracellular site of action of phenylalkylamines on L-type calcium current in rat ventricular myocytes.
Topics: Animals; Binding Sites; Calcium Channel Blockers; Calcium Channels; Cell Membrane; Gallopamil; Heart Ventricles; Patch-Clamp Techniques; Rats; Rats, Sprague-Dawley; Verapamil | 1995 |
Action of tertiary phenylalkylamines on cardiac transient outward current from outside the cell membrane.
Topics: Animals; Gallopamil; Heart; Hydrogen-Ion Concentration; Rats; Rats, Sprague-Dawley; Verapamil | 1996 |
L-type Ca2+ channel antagonists block voltage-dependent Ca2+ channels in identified leech neurons.
Topics: Animals; Caffeine; Calcium Channel Blockers; Calcium Channels, L-Type; Diltiazem; Gallopamil; Leeches; Membrane Potentials; Neurons; Nifedipine; Phosphodiesterase Inhibitors; Verapamil | 2004 |
Opposite effects of a single IIIS5 mutation on phenylalkylamine and dihydropyridine interaction with L-type Ca2+ channels.
Topics: Animals; Brain; Calcium; Calcium Channels; Calcium Channels, L-Type; Carrier Proteins; Cell Membrane; Dihydropyridines; DNA, Complementary; Dose-Response Relationship, Drug; Electrophysiology; Gallopamil; Homozygote; In Situ Hybridization; Isradipine; Kinetics; Mice; Mice, Transgenic; Microsomes; Models, Biological; Mutation; Oocytes; Protein Binding; Protein Structure, Tertiary; Recombinant Proteins; RNA, Complementary; Steroid Isomerases; Tyrosine; Verapamil; Xenopus laevis | 2004 |
Pharmacophoric features and Ca2+ ion holding capacity of verapamil.
Topics: Calcium; Calcium Channel Blockers; Gallopamil; Hydrogen Bonding; Models, Molecular; Molecular Conformation; Verapamil | 2005 |
Structural model for phenylalkylamine binding to L-type calcium channels.
Topics: Amino Acid Sequence; Binding Sites; Calcium Channel Blockers; Calcium Channels, L-Type; Computer Simulation; Dihydropyridines; Gallopamil; Models, Molecular; Molecular Sequence Data; Molecular Structure; Monte Carlo Method; Protein Structure, Tertiary; Sequence Alignment; Structure-Activity Relationship; Verapamil | 2009 |