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Dexverapamil

Known as: R verapamil, R-Verapamil 
The R-enantiomer of the calcium channel blocker verapamil. Dexverapamil competitively inhibits the multidrug resistance efflux pump P-glycoprotein… 
National Institutes of Health

Papers overview

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2006
2006
In order to evaluate dexverapamil as a resistance modifier in acute myeloid leukaemia, we have added dexverapamil (4×300 mg/d… 
2006
2006
Resistance to cytotoxic chemotherapy is a major problem in the management of patients with metastatic breast cancer. Various data… 
1999
1999
AbstractObjective: To determine the effect of the coadministration of the multidrug resistance (MDR) modulators cyclosporin A… 
1999
1999
Background: To study the effect of the resistance-modifying agent (RMA) dexverapamil on the pharmacokinetics and metabolism of… 
1997
1997
The concepts of stereochemistry and chirality are introduced, and the ability to distinguish among the different receptors caused… 
1996
1996
Injectable and infusion formulations of dexverapamil are evaluated for their potential to produce phlebitis. The evaluation… 
1996
1996
Reversal of drug resistance offers the hope of increasing the efficacy of conventional chemotherapy. We tested dexverapamil as a… 
1996
1996
A series of different human MDR (multidrug-resistant) cell lines including a HeLa-MDR1 transfectant which exhibit high… 
1995
1995
The pKa and intrinsic solubility of monomeric dexverapamil were determined from its pH-solubility profile to be 8.90 and 6.6 x 10…