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。