Stereoselective binding of tertatolol and of 4-hydroxytertatolol to human plasma proteins

Eur J Drug Metab Pharmacokinet. 1992 Jul-Sep;17(3):233-6. doi: 10.1007/BF03190151.

Abstract

The binding of racemic tertatolol and 4-hydroxytertatolol and of their enantiomers was compared in alpha 1-acid glycoprotein and albumin solutions. The binding rate of S(-)tertatolol to alpha 1-acid glycoprotein was much greater than that of R(+)tertatolol, the binding of the racemate being intermediate. It was the reverse for the binding to albumin, although the differences were slight. The binding of 4-hydroxytertatolol racemate and enantiomers was very low as compared to the binding of tertatolol, and there were no statistically significant differences in the binding of the 4-hydroxytertatolol enantiomers to either alpha 1-acid glycoprotein or albumin.

Publication types

  • Comparative Study

MeSH terms

  • Adrenergic beta-Antagonists / blood*
  • Binding Sites
  • Blood Proteins / metabolism*
  • Humans
  • Kinetics
  • Orosomucoid / metabolism
  • Propanolamines / blood*
  • Serum Albumin / metabolism
  • Stereoisomerism
  • Thiophenes*

Substances

  • Adrenergic beta-Antagonists
  • Blood Proteins
  • Orosomucoid
  • Propanolamines
  • Serum Albumin
  • Thiophenes
  • 4-hydroxytertatolol
  • tertatolol