作者:R. Jaques、A. Rossi、E. Urech、H. J. Bein、K. Hoffmann
DOI:10.1002/hlca.19590420422
日期:——
The synthesis and pharmacological activity of basically substituted dibenzothiazepines are described. They possess interesting antihistamine and antiserotonine activity. By varying the substituents in the benzene nuclei, and by a suitable choice the basic side chains, the specifity and activity of some derivatives could be increased considerably, especially with the dibenzothiazepinones.
描述了基本取代的二苯并硫氮杂s的合成和药理活性。它们具有有趣的抗组胺药和抗血清素活性。通过改变在苯核的替代物,并且通过合适的选择的碱性侧链,一些衍生物的特异性和活性,可以显着地增加,特别是与dibenzothiazepinones。