The present invention relates to fused pyrrole compounds of the formula 1.
1
in which at least one of the radicals R1, R2, R3 is 4-sulphur-substituted phenyl.
These compounds are in particular pyrrolizines, indolizines and heteroanalogues having selective inhibitory action on isoenzyme-2 of prostaglandin H synthase (COX-2). The invention also relates to pharmaceutical compositions which contain these compounds; and the use of these compounds for the treatment of disorders of the rheumatic type.
本发明涉及式1.1的融合
吡咯化合物,其中至少一个基团R1、R2、R3是4-
硫代取代
苯基。这些化合物特别是
吡咯啉、
吲哚啉和杂环类似物,具有对
前列腺素H
合成酶同工酶2的选择性抑制作用。本发明还涉及含有这些化合物的药物组合物;以及使用这些化合物治疗风湿性疾病的方法。