Nakamura S, Minami A, Nakata K, Kurobe N, Kouno K, Sakaguchi Y, Kashimoto S, Yoshida H, Kojima T, Ohue T
Research Laboratories, Dainippon Pharmaceutical Co., Ltd., Osaka, Japan.
Antimicrob Agents Chemother. 1989 Aug;33(8):1167-73. doi: 10.1128/AAC.33.8.1167.
AT-4140, 5-amino-1-cyclopropyl-6,8-difluoro-1,4-dihydro-7-(cis-3,5- dimethyl-1-piperazinyl)-4-oxoquinoline-3-carboxylic acid, showed broad and potent antibacterial activity. Its MICs for 90% of the strains tested were 0.1 to 0.78 micrograms/ml against gram-positive organisms, such as members of the genera Staphylococcus, Streptococcus, and Enterococcus, and 0.0125 to 1.56 micrograms/ml against gram-negative organisms, such as members of the family Enterobacteriaceae and the genera Pseudomonas, Branhamella, Campylobacter, Haemophilus, and Neisseria. Its MICs were 0.025 to 0.78 micrograms/ml against glucose nonfermenters, such as members of the genera Xanthomonas, Acinetobacter, Alcaligenes, Moraxella, Flavobacterium, and Brucella; 0.2 to 0.78 micrograms/ml against anaerobes, such as Clostridium perfringens and Bacteroides fragilis; 0.0125 to 0.05 micrograms/ml against Legionella spp.; 0.0125 to 0.2 micrograms/ml against Mycoplasma spp.; 0.031 to 0.063 micrograms/ml against Chlamydia spp.; and 0.1 to 0.3 micrograms/ml against Mycobacterium spp. The potencies of AT-4140 against gram-negative organisms were comparable to those of ciprofloxacin and higher than those of ofloxacin, enoxacin, and norfloxacin. The potencies of AT-4140 against gram-positive organisms, glucose nonfermenters, anaerobes, Mycoplasma spp., Chlamydia spp., and Mycobacterium spp. were generally higher than those of the quinolones with which AT-4140 was compared. AT-4140 showed good oral efficacy against systemic infections with Staphylococcus aureus, Streptococcus pyogenes, Streptococcus pneumoniae, Escherichia coli, and Pseudomonas aeruginosa in mice. Its efficacy was better when a daily dose was given once than when it was given in two doses. Good efficacies of the orally administered drug were also observed in pulmonary, dermal, and urinary tract infection models in mice. The in vivo efficacies of AT-4140 were equal to or better than those of ciprofloxacin, ofloxacin, enoxacin, and norfloxacin.
AT-4140,即5-氨基-1-环丙基-6,8-二氟-1,4-二氢-7-(顺式-3,5-二甲基-1-哌嗪基)-4-氧代喹啉-3-羧酸,显示出广泛且强效的抗菌活性。对于90%的受试菌株,其针对革兰氏阳性菌(如葡萄球菌属、链球菌属和肠球菌属的成员)的最低抑菌浓度(MIC)为0.1至0.78微克/毫升,针对革兰氏阴性菌(如肠杆菌科的成员以及假单胞菌属、布兰汉菌属、弯曲杆菌属、嗜血杆菌属和奈瑟菌属的成员)的MIC为0.0125至1.56微克/毫升。其针对葡萄糖非发酵菌(如黄单胞菌属、不动杆菌属、产碱杆菌属、莫拉菌属、黄杆菌属和布鲁菌属的成员)的MIC为0.025至0.78微克/毫升;针对厌氧菌(如产气荚膜梭菌和脆弱拟杆菌)的MIC为0.2至0.78微克/毫升;针对军团菌属的MIC为0.0125至0.05微克/毫升;针对支原体属的MIC为0.0125至0.2微克/毫升;针对衣原体属的MIC为0.031至0.063微克/毫升;针对分枝杆菌属的MIC为0.1至0.3微克/毫升。AT-4140对革兰氏阴性菌的效力与环丙沙星相当,且高于氧氟沙星、依诺沙星和诺氟沙星。AT-4140对革兰氏阳性菌、葡萄糖非发酵菌、厌氧菌、支原体属、衣原体属和分枝杆菌属的效力通常高于与之比较的喹诺酮类药物。AT-4140对小鼠体内由金黄色葡萄球菌、化脓性链球菌、肺炎链球菌、大肠杆菌和铜绿假单胞菌引起的全身感染显示出良好的口服疗效。每日剂量单次给药时的疗效优于分两次给药时的疗效。在小鼠的肺部、皮肤和尿路感染模型中也观察到口服该药具有良好疗效。AT-4140的体内疗效等于或优于环丙沙星、氧氟沙星、依诺沙星和诺氟沙星。