Dihydropyrimidine calcium channel blockers. 2. 3-substituted-4-aryl-1,4-dihydro-6-methyl-5-pyrimidinecarboxylic acid esters as potent mimics of dihydropyridines. 1990

K S Atwal, and G C Rovnyak, and S D Kimball, and D M Floyd, and S Moreland, and B N Swanson, and J Z Gougoutas, and J Schwartz, and K M Smillie, and M F Malley
Squibb Institute for Medical Research, Princeton, New Jersey 08543-4000.

To enhance the intrinsic potency of dihydropyrimidine calcium channel blockers, we have modified the structure of previously described 2-heteroalkyl-1,4-dihydropyrimidines 2 to 3-substituted 1,4-dihydropyrimidines 3. Structure-activity studies using potassium-depolarized rabbit aorta show that ortho, meta-disubstituted aryl derivatives are more potent than either ortho- or meta-monosubstituted compounds. While vasorelaxant activity was critically dependent on the size of the C5 ester group, isopropyl ester being the best, a variety of substituents (carbamate, acyl, sulfonyl, alkyl) were tolerated at N3. Our results show dihydropyrimidines 3 are significantly more potent than corresponding 2-heteroalkyl-1,4-dihydropyrimidines 2 and only slightly less potent than similarly substituted 2-heteroalkyl-1,4-dihydropyridines 4 and 5. Whereas dihydropyridine enantiomers usually show 10-15-fold difference in activity, the enantiomers of dihydropyrimidine 3j show more than a 1000-fold difference in activity. These results strengthen the requirement of an enamino ester for binding to the dihydropyridine receptor and indicate a nonspecific role for the N3-substituent.

UI MeSH Term Description Entries
D008297 Male Males
D009131 Muscle, Smooth, Vascular The nonstriated involuntary muscle tissue of blood vessels. Vascular Smooth Muscle,Muscle, Vascular Smooth,Muscles, Vascular Smooth,Smooth Muscle, Vascular,Smooth Muscles, Vascular,Vascular Smooth Muscles
D011743 Pyrimidines A family of 6-membered heterocyclic compounds occurring in nature in a wide variety of forms. They include several nucleic acid constituents (CYTOSINE; THYMINE; and URACIL) and form the basic structure of the barbiturates.
D011817 Rabbits A burrowing plant-eating mammal with hind limbs that are longer than its fore limbs. It belongs to the family Leporidae of the order Lagomorpha, and in contrast to hares, possesses 22 instead of 24 pairs of chromosomes. Belgian Hare,New Zealand Rabbit,New Zealand Rabbits,New Zealand White Rabbit,Rabbit,Rabbit, Domestic,Chinchilla Rabbits,NZW Rabbits,New Zealand White Rabbits,Oryctolagus cuniculus,Chinchilla Rabbit,Domestic Rabbit,Domestic Rabbits,Hare, Belgian,NZW Rabbit,Rabbit, Chinchilla,Rabbit, NZW,Rabbit, New Zealand,Rabbits, Chinchilla,Rabbits, Domestic,Rabbits, NZW,Rabbits, New Zealand,Zealand Rabbit, New,Zealand Rabbits, New,cuniculus, Oryctolagus
D011919 Rats, Inbred Strains Genetically identical individuals developed from brother and sister matings which have been carried out for twenty or more generations or by parent x offspring matings carried out with certain restrictions. This also includes animals with a long history of closed colony breeding. August Rats,Inbred Rat Strains,Inbred Strain of Rat,Inbred Strain of Rats,Inbred Strains of Rats,Rat, Inbred Strain,August Rat,Inbred Rat Strain,Inbred Strain Rat,Inbred Strain Rats,Inbred Strains Rat,Inbred Strains Rats,Rat Inbred Strain,Rat Inbred Strains,Rat Strain, Inbred,Rat Strains, Inbred,Rat, August,Rat, Inbred Strains,Rats Inbred Strain,Rats Inbred Strains,Rats, August,Rats, Inbred Strain,Strain Rat, Inbred,Strain Rats, Inbred,Strain, Inbred Rat,Strains, Inbred Rat
D002121 Calcium Channel Blockers A class of drugs that act by selective inhibition of calcium influx through cellular membranes. Calcium Antagonists, Exogenous,Calcium Blockaders, Exogenous,Calcium Channel Antagonist,Calcium Channel Blocker,Calcium Channel Blocking Drug,Calcium Inhibitors, Exogenous,Channel Blockers, Calcium,Exogenous Calcium Blockader,Exogenous Calcium Inhibitor,Calcium Channel Antagonists,Calcium Channel Blocking Drugs,Exogenous Calcium Antagonists,Exogenous Calcium Blockaders,Exogenous Calcium Inhibitors,Antagonist, Calcium Channel,Antagonists, Calcium Channel,Antagonists, Exogenous Calcium,Blockader, Exogenous Calcium,Blocker, Calcium Channel,Blockers, Calcium Channel,Calcium Blockader, Exogenous,Calcium Inhibitor, Exogenous,Channel Antagonist, Calcium,Channel Blocker, Calcium,Inhibitor, Exogenous Calcium
D002621 Chemistry A basic science concerned with the composition, structure, and properties of matter; and the reactions that occur between substances and the associated energy exchange.
D004095 Dihydropyridines Pyridine moieties which are partially saturated by the addition of two hydrogen atoms in any position.
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D013329 Structure-Activity Relationship The relationship between the chemical structure of a compound and its biological or pharmacological activity. Compounds are often classed together because they have structural characteristics in common including shape, size, stereochemical arrangement, and distribution of functional groups. Relationship, Structure-Activity,Relationships, Structure-Activity,Structure Activity Relationship,Structure-Activity Relationships

Related Publications

K S Atwal, and G C Rovnyak, and S D Kimball, and D M Floyd, and S Moreland, and B N Swanson, and J Z Gougoutas, and J Schwartz, and K M Smillie, and M F Malley
February 1991, Journal of medicinal chemistry,
K S Atwal, and G C Rovnyak, and S D Kimball, and D M Floyd, and S Moreland, and B N Swanson, and J Z Gougoutas, and J Schwartz, and K M Smillie, and M F Malley
April 1987, Journal of medicinal chemistry,
K S Atwal, and G C Rovnyak, and S D Kimball, and D M Floyd, and S Moreland, and B N Swanson, and J Z Gougoutas, and J Schwartz, and K M Smillie, and M F Malley
August 2008, Acta crystallographica. Section E, Structure reports online,
K S Atwal, and G C Rovnyak, and S D Kimball, and D M Floyd, and S Moreland, and B N Swanson, and J Z Gougoutas, and J Schwartz, and K M Smillie, and M F Malley
February 1983, FEBS letters,
K S Atwal, and G C Rovnyak, and S D Kimball, and D M Floyd, and S Moreland, and B N Swanson, and J Z Gougoutas, and J Schwartz, and K M Smillie, and M F Malley
August 2013, Iranian journal of basic medical sciences,
K S Atwal, and G C Rovnyak, and S D Kimball, and D M Floyd, and S Moreland, and B N Swanson, and J Z Gougoutas, and J Schwartz, and K M Smillie, and M F Malley
February 2012, Archiv der Pharmazie,
K S Atwal, and G C Rovnyak, and S D Kimball, and D M Floyd, and S Moreland, and B N Swanson, and J Z Gougoutas, and J Schwartz, and K M Smillie, and M F Malley
July 1991, Journal of medicinal chemistry,
K S Atwal, and G C Rovnyak, and S D Kimball, and D M Floyd, and S Moreland, and B N Swanson, and J Z Gougoutas, and J Schwartz, and K M Smillie, and M F Malley
February 2002, Farmaco (Societa chimica italiana : 1989),
K S Atwal, and G C Rovnyak, and S D Kimball, and D M Floyd, and S Moreland, and B N Swanson, and J Z Gougoutas, and J Schwartz, and K M Smillie, and M F Malley
May 1998, Journal of medicinal chemistry,
K S Atwal, and G C Rovnyak, and S D Kimball, and D M Floyd, and S Moreland, and B N Swanson, and J Z Gougoutas, and J Schwartz, and K M Smillie, and M F Malley
December 2005, European journal of medicinal chemistry,
Copied contents to your clipboard!