Abstract
Thirteen 3-acetyl-4-aryl-5-oxo-2,7,7-trimethyl-1,4,5,6,7,8- hexahydroquinoline derivatives (5a-m), one of which was synthesized before, have been prepared. The structures of the products 5b-m were characterized by IR,1H-NMR and elemental analysis. The calcium antagonistic activity of these compounds was studied in rabbit taenia coli precontracted with 1 mmol/l Ca+2.
MeSH terms
-
Animals
-
Calcium Channel Blockers / chemical synthesis*
-
Calcium Channel Blockers / chemistry
-
Calcium Channel Blockers / pharmacology
-
Female
-
Guinea Pigs
-
In Vitro Techniques
-
Magnetic Resonance Spectroscopy
-
Male
-
Molecular Weight
-
Muscle Contraction / drug effects
-
Muscle, Smooth / drug effects
-
Nicardipine / pharmacology
-
Quinolines / chemical synthesis*
-
Quinolines / chemistry
-
Quinolines / pharmacology
-
Rabbits
Substances
-
Calcium Channel Blockers
-
Quinolines
-
Nicardipine