Malabarba A, Berti M, De Paoli A, Cavalleri B
Farmaco Sci. 1979 Feb;34(2):105-18.
The synthesis of 7-[[(1-methyl-2-nitro-1H-imidazol-5-yl)methylene]amino] and 7-[[(2-amino-1-methyl-1H-imidazol-5-yl)methyle-ne]amino]cephalosporanic acids and of some derivatives is described. Their physico-chemical characteristics are reported. The compounds show no appreciable antibacterial activity in vitro. They show no synergy with cephaloridine against Enterobacter cloacae 214 (producer of class I beta-lactamase) and therefore have no anti-beta-lactamase activity.
描述了7-[[(1-甲基-2-硝基-1H-咪唑-5-基)亚甲基]氨基]和7-[[(2-氨基-1-甲基-1H-咪唑-5-基)亚甲基]氨基]头孢烷酸及其一些衍生物的合成。报道了它们的物理化学特性。这些化合物在体外没有明显的抗菌活性。它们与头孢噻啶对阴沟肠杆菌214(I类β-内酰胺酶产生菌)没有协同作用,因此没有抗β-内酰胺酶活性。