Cardiovascular hybrid drugs: new benzazepinone derivatives as bradycardic agents endowed with selective β 1 -Non-competitive antagonism
摘要:
The synthesis and pharmacological profile of some hybrid compounds bearing both the benzazepinone moiety present in Zatebradine and typical P-blocker aryloxypropanolamine groups are described. The new compounds proved to be endowed with negative chronotropic and inotropic activity and are weak vasorelaxant agents. The cardiodepressant action is probably due to selective beta(1)-noncompetitive reversible antagonism. Both enantiomers of the most active compound 5c were synthesized and they showed a different cardiovascular profile, that is (+)-(R)-enantiomer displays affinity for cardiac beta(1)-adrenoceptors, while (-)-(S)-enantiomer shows specificity for vessel smooth muscle. (C) 2003 Elsevier Science Ltd. All rights reserved.
Absolute configuration of glycerol derivatives. 3. Synthesis and Cupra A circular dichroism spectra of some chiral 3-aryloxy-1,2-propanediols and 3-aryloxy-1-amino-2-propanols
作者:Wendel L. Nelson、John E. Wennerstrom、S. Raman Sankar
DOI:10.1021/jo00426a016
日期:1977.3
Cardiovascular hybrid drugs: new benzazepinone derivatives as bradycardic agents endowed with selective β 1 -Non-competitive antagonism
The synthesis and pharmacological profile of some hybrid compounds bearing both the benzazepinone moiety present in Zatebradine and typical P-blocker aryloxypropanolamine groups are described. The new compounds proved to be endowed with negative chronotropic and inotropic activity and are weak vasorelaxant agents. The cardiodepressant action is probably due to selective beta(1)-noncompetitive reversible antagonism. Both enantiomers of the most active compound 5c were synthesized and they showed a different cardiovascular profile, that is (+)-(R)-enantiomer displays affinity for cardiac beta(1)-adrenoceptors, while (-)-(S)-enantiomer shows specificity for vessel smooth muscle. (C) 2003 Elsevier Science Ltd. All rights reserved.
Absolute configuration of 3-aryloxypropane-1,2-diols and derivatives: mephenesin isomers
作者:Wendel L. Nelson、Carl E. Wood
DOI:10.1039/c39730000896
日期:——
The optical isomers of mephenesin (3-o-tolylpropane-1,2-diol) were prepared from 2R- and 2S-3-tosyloxypropane-1,2-diol acetonide by reaction with o-cresol(NaOH) and the configurations confirmed on the basis of c.d. spectra in Cupra A Solution.
由2 R-和2 S -3-甲苯磺酰氧基丙烷-1,2-二醇丙酮化物与邻甲酚(NaOH)反应制得美芬素(3-邻甲苯基丙烷-1,2-二醇)的旋光异构体根据Cupra A解决方案中的cd光谱确定。