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Desacetyl-Diltiazem Displays Severalfold Higher Affinity to CYP2D6 Compared with CYP3A4

Espen Molden, Anders Åsberg and Hege Christensen
Drug Metabolism and Disposition January 2002, 30 (1) 1-3; DOI: https://doi.org/10.1124/dmd.30.1.1

Article Information

vol. 30 no. 1 1-3
DOI 
https://doi.org/10.1124/dmd.30.1.1
PubMed 
11744603
Published By 
American Society for Pharmacology and Experimental Therapeutics
Print ISSN 
0090-9556
Online ISSN 
1521-009X
History 
  • Received June 13, 2001
  • Accepted September 20, 2001
  • Published online January 1, 2002.
Copyright & Usage 
The American Society for Pharmacology and Experimental Therapeutics

Author Information

  1. Espen Molden1,
  2. Anders Åsberg2 and
  3. Hege Christensen1
  1. 1Department of Pharmacology, School of Pharmacy, University of Oslo, Oslo, Norway (E.M., H.C.); 2Laboratory for Renal Physiology, Section of Nephrology, Medical Department, National Hospital, University of Oslo, Oslo, Norway (A. Å.)
  1. Espen Molden, Department of Pharmacology, School of Pharmacy, University of Oslo, P.O. Box 1068 Blindern, N-0316 Oslo, Norway. E-mail: espen.molden{at}farmasi.uio.no
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Rapid CommunicationShort Communication

Desacetyl-Diltiazem Displays Severalfold Higher Affinity to CYP2D6 Compared with CYP3A4

Espen Molden, Anders Åsberg and Hege Christensen
Drug Metabolism and Disposition January 1, 2002, 30 (1) 1-3; DOI: https://doi.org/10.1124/dmd.30.1.1
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