The present invention relates to novel N-substituted azaheterocyclic compounds of the general formula wherein X, Y, Z, R.sup.1, R.sup.2 and r are as defined in the detailed part of the present description, or salts thereof, to methods for their preparation, to compositions containing them, and to their use for the clinical treatment of painful, hyperalgesic and/or inflammatory conditions in which C-fibers play a pathophysiological role by eliciting neurogenic pain or inflammation as well as their use for treatment of indications caused by or related to the secretion and circulation of insulin antagonizing peptides, e.g. non-insulin-dependent diabetes mellitus (NIDDM) and ageing-associated obesity.
本发明涉及新型N-取代的杂氮
杂环化合物的一般式,其中X、Y、Z、R.sup.1、R.sup.2和r在本说明书的详细部分中定义,或其盐,以及它们的制备方法、含有它们的组合物以及它们用于治疗C纤维在病理生理学作用中通过引发神经源性疼痛或炎症的疼痛、高痛觉和/或炎症状况的临床治疗,以及它们用于治疗由
胰岛素拮抗肽分泌和循环引起或相关的指示,例如非
胰岛素依赖性糖尿病(NID
DM)和与衰老相关的肥胖症。