Rose U
Institute for Pharmacy, Johannes Gutenberg University of Mainz, FRG.
Pharm Acta Helv. 1990;65(7):178-85. doi: 10.1002/chin.199052195.
The vinylogous, anellated and non-anellated dihydropyridines 4 and their coupled analogues 5 are accessible through Hantzsch-type cyclization reactions. IR, 1H-NMR, and mass spectral data are in agreement with the postulated structures. Pharmacological investigations on electrically-stimulated left atria of guinea pigs with some of the compounds gave rise to positive inotropic activities whereas BaCl2-induced contractions of the ileum were inhibited in a dose-dependent manner by some of the products.
乙烯型、环化和非环化的二氢吡啶4及其偶联类似物5可通过汉茨施型环化反应制得。红外光谱、¹H-核磁共振光谱和质谱数据与推测的结构相符。用其中一些化合物对豚鼠电刺激的左心房进行的药理学研究产生了正性肌力活性,而一些产物对氯化钡诱导的回肠收缩具有剂量依赖性抑制作用。