Antihypertensive activity of substituted 2,3,8,8a-tetrahydro-7H-oxazolo[3,2-a]pyridinedicarboxylate enantiomers

Bioorg Med Chem Lett. 2000 Feb 21;10(4):319-22. doi: 10.1016/s0960-894x(99)00691-5.

Abstract

The synthesis and antihypertensive activity of racemates and enantiomers of substituted 2,3,8,8a-tetrahydro-7H-oxazolo[3,2-a]pyridinedicarboxylates have been reported.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antihypertensive Agents / chemistry*
  • Antihypertensive Agents / pharmacokinetics
  • Antihypertensive Agents / therapeutic use*
  • Blood Pressure / drug effects
  • Drug Evaluation
  • Heart Rate / drug effects
  • Male
  • Nifedipine / pharmacokinetics
  • Nifedipine / therapeutic use
  • Oxazoles / chemistry*
  • Oxazoles / pharmacokinetics
  • Oxazoles / therapeutic use*
  • Pyridines / chemistry*
  • Pyridines / pharmacokinetics
  • Pyridines / therapeutic use*
  • Rats
  • Rats, Inbred SHR
  • Stereoisomerism
  • Structure-Activity Relationship
  • Time Factors

Substances

  • Antihypertensive Agents
  • Oxazoles
  • Pyridines
  • Nifedipine