Cousse H, Mouzin G, Bonnaud B, Tarayre J P, Couzinier J P
Arzneimittelforschung. 1986 Sep;36(9):1391-3.
25 arylthiazole oxamate derivatives were synthesized and examined for antiallergic activity in the rat passive cutaneous anaphylaxis assay. These compounds were prepared by treatment of the appropriate bromoacetophenone with thioureas to give arylaminothiazoles. Further condensation with alkyloxalyl chloride gave the arylthiazolyl oxamates. Several derivatives showed a 70% inhibition at 5 mg/kg p.o. p-Alkoxy substitution on the phenyl ring resulted in enhanced activity while N-alkyl substitution on the nitrogen amide function inhibited the activity. Ethyl-N-(4-p-methoxyphenyl)-2-thiazolyl oxamate (tioxamast, F-1865) was selected for clinical studies.
合成了25种芳基噻唑草氨酸酯衍生物,并在大鼠被动皮肤过敏试验中检测其抗过敏活性。这些化合物是通过用硫脲处理适当的溴代苯乙酮得到芳基氨基噻唑来制备的。再与烷基草酰氯缩合得到芳基噻唑基草氨酸酯。几种衍生物在口服5mg/kg时显示出70%的抑制率。苯环上的对烷氧基取代导致活性增强,而氮酰胺官能团上的N-烷基取代则抑制活性。选择N-(4-对甲氧基苯基)-2-噻唑基乙草氨酸酯(替奥司特,F-1865)进行临床研究。