Brufani M, Cellai L, Cerrini S, Fedeli W, Segre A, Vaciago A
Mol Pharmacol. 1982 Mar;21(2):394-9.
The X-ray and NMR structural study of 3-carbomethoxy rifamycin S5 was undertaken in order to determine whether its low antimicrobial activity was related to a conformation of the molecule which was unfavorable for interaction with bacterial DNA-dependent RNA polymerase. However, the molecule assumes a conformation similar to that of the active rifamycins. Indeed the compound was found to be active on the isolated enzyme, so that its low activity on whole bacteria has to be attributed to factors affecting its penetration through the bacterial cell wall.
对3-甲氧羰基利福霉素S5进行了X射线和核磁共振结构研究,以确定其低抗菌活性是否与分子构象有关,这种构象不利于与细菌DNA依赖性RNA聚合酶相互作用。然而,该分子呈现出与活性利福霉素相似的构象。实际上,该化合物在分离出的酶上具有活性,因此其对完整细菌的低活性必定归因于影响其穿透细菌细胞壁的因素。