The invention relates to a group of new substituted 1,7-annelated 1H-indazole derivatives being strong and selective antagonists of "neuronal" 5-hydroxytryptamine (5-HT) receptors. The compounds can be represented by general formula 1: ##STR1##
该发明涉及一组新的取代的1,7-环化1H-
吲唑衍
生物,它们是"神经元"5-羟
色胺(5-HT)受体的强烈和选择性拮抗剂。这些化合物可以用一般式1表示:##STR1##