Heinisch Lothar, Wittmann Steffen, Stoiber Thomas, Berg Albrecht, Ankel-Fuchs Dorothe, Möllmann Ute
Hans Knöll-Institute for Natural Products Research, Jena, Germany.
J Med Chem. 2002 Jul 4;45(14):3032-40. doi: 10.1021/jm010546b.
New acylated bis-catecholates and 1,3-benzoxazine-2,4-dione derivatives based on secondary diamino acids (N-(aminoalkyl)glycines, N-aminopropyl-alanine, and N-aminopropyl-4-aminovaleric acid), on N-(aminoalkyl)aminomethyl benzoic acids, on N-(aminoalkyl)aminomethyl phenoxyacetic acids, or on 3,5-diaminobenzoic acid were synthesized as artificial siderophores. The corresponding diamino acids were obtained from the diamines and oxocarboxylic acids by catalytic hydrogenation. The acylated bis-catecholates and 1,3-benzoxazine-2,4-diones were coupled with ampicillin or amoxicillin to new siderophore aminoacylpenicillin conjugates. These conjugates exhibited very strong antibacterial activity in vitro against Gram-negative bacterial pathogens including Pseudomonas aeruginosa, Stenotrophomonas maltophilia, Escherichia coli, Klebsiella pneumoniae, and Serratia marcescens. The ampicillin derivative 7b (HKI 9924154) and the corresponding amoxicillin derivative 8 (HKI 9924155) represent the most active compounds. The conjugates can use bacterial iron siderophore uptake routes to penetrate the Gram-negative outer membrane permeability barrier. This was demonstrated by assays with mutants deficient in components of the iron transport systems. New siderophore penicillin V conjugates with the siderophore component attached to the phenyl ring of penicillin V are inactive against these Gram-negative bacteria.
基于仲二氨基酸(N-(氨基烷基)甘氨酸、N-氨基丙基丙氨酸和N-氨基丙基-4-氨基戊酸)、N-(氨基烷基)氨基甲基苯甲酸、N-(氨基烷基)氨基甲基苯氧基乙酸或3,5-二氨基苯甲酸合成了新型酰化双儿茶酚酯和1,3-苯并恶嗪-2,4-二酮衍生物作为人工铁载体。相应的二氨基酸通过催化氢化由二胺和氧代羧酸制得。将酰化双儿茶酚酯和1,3-苯并恶嗪-2,4-二酮与氨苄青霉素或阿莫西林偶联,得到新型铁载体氨基酰基青霉素缀合物。这些缀合物在体外对革兰氏阴性细菌病原体表现出非常强的抗菌活性,包括铜绿假单胞菌、嗜麦芽窄食单胞菌、大肠杆菌、肺炎克雷伯菌和粘质沙雷氏菌。氨苄青霉素衍生物7b(HKI 9924154)和相应的阿莫西林衍生物8(HKI 9924155)是活性最强的化合物。这些缀合物可以利用细菌铁载体摄取途径穿透革兰氏阴性菌外膜通透性屏障。这通过对铁转运系统成分缺陷的突变体进行的试验得到了证明。铁载体成分连接在青霉素V苯环上的新型铁载体青霉素V缀合物对这些革兰氏阴性菌无活性。