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Tiapamil

National Institutes of Health

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Tiapamil Hydrochloride

Papers overview

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1994
1994
Identification of a multidrug resistance modulator with clinical potential by analysis of synergistic activity in vitro, toxicity in vivo and growth delay in a solid human tumour xenograft.
Highly Cited
1991
Highly Cited
1991
Agents which reverse multidrug-resistance are inhibitors of [3H]vinblastine transport by isolated vesicles.
Review
1988
Review
1988
Pharmacokinetics of Calcium Antagonists Under Development
SummaryCalcium antagonist drugs under clinical development are of the Type I (verapamil, diltiazem-like) and Type II (nifedipine… 
1986
1986
Comparative Acute Effects of the Calcium Channel Blockers Tiapamil, Nisoldipine, and Nifedipine on Blood Pressure and Some Regulatory Factors in Normal and Hypertensive Subjects
Summary: To clarify the pharmacological profile of the two new calcium channel blockers tiapamil and nisoldipine in humans, their… 
1985
1985
Promotion of daunorubicin uptake and toxicity by the calcium antagonist tiapamil and its analogs.
Studies were performed with the anthracycline-responsive P388 murine leukemia cell line, and with P388/ADR, a subline selected… 
1985
1985
Tiapamil, a new calcium antagonist: hemodynamic effects in patients with acute myocardial infarction.
The afterload reduction and myocardial oxygen sparing that results after administration of calcium antagonists suggests a… 
Highly Cited
1983
Highly Cited
1983
Temperature‐dependent regulation of d‐cis‐[3H]diltiazem binding to Ca2+ channels by 1,4‐dihydropyridine channel agonists and antagonists
1983
1983
Interaction between digoxin and the calcium antagonists nicardipine and tiapamil.
The investigation was designed to test whether nicardipine and tiapamil interact with digoxin, resulting in increased plasma… 
Highly Cited
1982
Highly Cited
1982
Characterization of [3H]nifedipine binding sites in rabbit myocardium.
1982
1982
Pharmacokinetics and metabolism of tiapamil.
The main pathways of biotransformation of tiapamil and basic pharmacokinetic information on the drug are presented and compared… 
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