Fardeau Sylvain, Dassonville-Klimpt Alexandra, Audic Nicolas, Sasaki André, Pillon Marine, Baudrin Emmanuel, Mullié Catherine, Sonnet Pascal
Laboratoire de Glycochimie, des Antimicrobiens, et des Agroressources, CNRS FRE 3517, UFR de Pharmacie, Université de Picardie Jules Verne, F-80037 Amiens, France.
Pharmamens, 9 avenue Théophile Gautier, 75016 Paris, France.
Bioorg Med Chem. 2014 Aug 1;22(15):4049-60. doi: 10.1016/j.bmc.2014.05.067. Epub 2014 Jun 12.
The development of an efficient route to obtain artificial siderophore-antibiotic conjugates active against Gram-negative bacteria is crucial. Herein, a practical access to triscatecholate enterobactin analogues linked to the ciprofloxacin along with their antibacterial evaluation are described. Two series of conjugates were obtained with and without a piperazine linker which is known to improve the pharmacokinetics profile of a drug. A monocatecholate-ciprofloxacin conjugate was also synthesized and evaluated. The antibacterial activities against Pseudomonas aeruginosa for some conjugates are related to the iron concentration in the culture medium and seem to depend on the bacterial iron uptake systems.
开发一种有效的途径来获得对革兰氏阴性菌有效的人工铁载体-抗生素缀合物至关重要。本文描述了一种与环丙沙星相连的三儿茶酚酸肠杆菌素类似物的实用合成方法及其抗菌评估。通过有无哌嗪连接基获得了两个系列的缀合物,已知哌嗪连接基可改善药物的药代动力学特征。还合成并评估了单儿茶酚酸-环丙沙星缀合物。一些缀合物对铜绿假单胞菌的抗菌活性与培养基中的铁浓度有关,似乎取决于细菌的铁摄取系统。