No Pharmacokinetic or Pharmacodynamic Interaction Between Theophylline and the Leukotriene Biosynthesis Inhibitor BAY x 1005

Author:

Groen Henk,Moesker Harm L.,Leeuwenkamp Oscar R.,Sollie Frans A. E.,Jonkman Jan H. G.

Publisher

Wiley

Subject

Pharmacology (medical),Pharmacology

Reference17 articles.

1. Mode of action of the new selective leukotriene synthesis inhibitor BAY × 1005 {(R)-2-[4-quinolin-2-yl-me-thoxy)phenyl]-2-cyclopentyl acetic acid} and structurally related compounds;Hatzelmann;Biochem Pharmacol,1993

2. BAY × 1005, a new inhibitor of leukotriene synthesis: in vivo inflammation pharmacology and pharmacokinetics;Müller-Peddinghaus;J Pharmacol Exp Ther,1993

3. In vitro pharmacology of BAY × 1005, a new inhibitor of leukotriene synthesis;Fruchtmann;Agents Actions,1993

4. Leukotrienes and other products of the 5-lipoxygenase pathway: biochemistry and relation to pathobiology in human diseases;Lewis;N Engl J Med,1990

5. Arachidonic acid metabolism: role in inflammation;Samuelsson;Z Rheumatol,1991

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