Wick W E, Preston D A, White W A, Gordee R S
Antimicrob Agents Chemother. 1973 Oct;4(4):415-20. doi: 10.1128/AAC.4.4.415.
Compound 64716, 1-ethyl-4 (1H)-oxo-[1,3]dioxolo[4,5-g]cinnoline-3-carboxylic acid, is a new synthetic antibacterial agent. The antibacterial spectrum of this compound includes gram-negative bacteria that are most frequently isolated from urinary tract infections. Minimal inhibitory concentration values of 64716 for isolates of Escherichia coli and Proteus sp. ranged from 2 to 4 and 2 to 8 mug/ml, respectively, and the compound was bactericidal at concentrations close to the minimal inhibitory concentration values. In vivo, doses required for successful therapy of experimental mouse infections were comparable to those for nalidixic acid. After oral administration of 40 mg/kg, peak concentrations of this compound in mouse blood reached 19.2 mug/ml. Within 30 min after doses of 20 mg/kg, bacteriologically active drug concentrations of 64716, nalidixic acid, and oxolinic acid in mouse urine were >1,000, 170, and <1.5 mug/ml, respectively. Resistant bacteria were not selected when bacteria were exposed to 500 mug/ml of 64716. Compound 64716 was less bound by human serum proteins than was nalidixic acid. Equivalent antibacterial activity along with superior pharmacological properties of 64716 when compared with nalidixic acid lead to the conclusion that this new compound is a promising antibacterial agent.
化合物64716,即1-乙基-4(1H)-氧代-[1,3]二氧杂环戊烯并[4,5-g]噌啉-3-羧酸,是一种新型合成抗菌剂。该化合物的抗菌谱包括最常从尿路感染中分离出的革兰氏阴性菌。化合物64716对大肠杆菌和变形杆菌属菌株的最低抑菌浓度值分别为2至4微克/毫升和2至8微克/毫升,且该化合物在接近最低抑菌浓度值的浓度下具有杀菌作用。在体内,成功治疗实验性小鼠感染所需的剂量与萘啶酸相当。口服40毫克/千克后,该化合物在小鼠血液中的峰值浓度达到19.2微克/毫升。在给予20毫克/千克剂量后的30分钟内,小鼠尿液中64716、萘啶酸和恶喹酸的具有细菌活性的药物浓度分别>1000、170和<1.5微克/毫升。当细菌暴露于500微克/毫升的64716时,未筛选出耐药菌。与萘啶酸相比,化合物64716与人类血清蛋白的结合较少。64716与萘啶酸相比具有同等的抗菌活性以及更优异的药理学特性,由此得出结论,这种新化合物是一种有前景的抗菌剂。