Prothioconazole 是具有抗真菌作用的含环丙烷的三唑化合物。Prothioconazole被描述为是脱甲基酶抑制剂，被发现是底物与atM的竞争性抑制剂。CYP51，将其作用与其他吡咯化合物的非竞争性抑制相分离。 Prothioconazole is a cyclopropane-containing triazole compound with antifungal effects. Prothioconazole is described to be a demethylase inhibitor and was found to be a competitive inhibitor of substrate binding at|M. graminicola|CYP51, separating its action from the noncompetitive inhibition of other azole compounds.