112795-97-8Relevant articles and documents
Synthesis and reactions of Biginelli-compounds. Part 23: Chemoenzymatic syntheses of enantiomerically pure 4-aryl-3,4-dihydropyrimidin-2(1H)-ones
Schnell, Barbara,Krenn, Wolfram,Faber, Kurt,Kappe, C. Oliver
, p. 4382 - 4389 (2007/10/03)
Enantiomerically pure dihydropyrimidones (DHPMs) were prepared by lipase-catalyzed enzymatic resolution of two types of activated DHPM esters. In the first model series, pivaloyloxymethyl-activated DHPM C5-esters 10a-c were resolved on an analytical scale
Dihydropyrimidine calcium channel blockers. 3. 3-carbamoyl-4-aryl-1,2,3,4-tetrahydro-6-methyl-5-pyrimidinecarboxylic acid esters as orally effective antihypertensive agents
Atwal,Swanson,Unger,Floyd,Moreland,Hedberg,O'Reilly
, p. 806 - 811 (2007/10/02)
In order to explain the potent antihypertensive activity of the modestly active (IC50 = 3.2 μM) dihydropyrimidine calcium channel blocker 5, we carried out drug metabolism studies in the rat and found 5 is metabolized to compounds 6-10. Two of