申请人:Parcor
公开号:US04104390A1
公开(公告)日:1978-08-01
This invention relates to pyridine derivatives of the formulae: ##STR1## in which R.sup.1 is hydrogen, lower alkyl, aralkyl optionally substituted on the aromatic nucleus with at least a halogen atom or a hydroxy, nitro, amino, cyano, carboxy, alkoxycarbonyl, lower alkyl, lower alkoxy or trifluoromethyl group; R.sup.2 is hydrogen or lower alkyl; and R.sup.3 is hydrogen or at least a substituent selected from a halogen atom, a hydroxy, lower alkyl and lower alkoxy group, and their pharmaceutically acceptable inorganic or organic acid addition salts. Said compounds have particularly an anti-inflammatory and blood-platelet aggregation inhibiting activity.
本发明涉及公式为:##STR1##的吡啶衍生物,其中R.sup.1为氢、较低的烷基、芳基烷基,其在芳香核上至少用卤原子或羟基、硝基、氨基、氰基、羧基、烷氧基羰基、较低的烷基、较低的烷氧基或三氟甲基基团进行取代;R.sup.2为氢或较低的烷基;R.sup.3为氢或至少从卤原子、羟基、较低的烷基和较低的烷氧基中选择的取代基,以及其在药学上可接受的无机或有机酸盐。该化合物特别具有抗炎和抑制血小板聚集的活性。