The present invention provides an azole compound represented by the formula (I):
, wherein Ar is an optionally-substituted phenyl group; R¹ and R² are, the same or different, a hydrogen atom or a lower alkyl group, or R¹ and R² may combine together to form a lower alkylene group; R³ is a hydrogen atom or an acyl group; Y is a nitrogen atom or a methine group; and A is an optionally-substituted saturated cyclic amide group bonded through a first nitrogen atom, or a salt thereof, which is useful for prevention and therapy of fungal infections of mammals as antifungal agent.
本发明提供了一种由式(I)表示的
唑类化合物:
其中,Ar 是任选取代的
苯基;R¹ 和 R² 是相同或不同的
氢原子或低级烷基,或 R¹ 和 R² 可结合在一起形成低级亚烷基;R³ 是
氢原子或酰基;Y 是
氮原子或
甲基;A 是通过第一个
氮原子键合的任选取代的饱和环状
酰胺基团,或其盐,可作为抗真菌剂用于预防和治疗哺乳动物的真菌感染。