Stefancich G, Corelli F, Massa S, Silvestri R, Panico S, Artico M, Simonetti N
Istituto di Chimica Farmaceutica e Tossicologica, Facolta di Farmacia, Università degli Studi di Roma La Sapienza.
Farmaco Sci. 1987 Jan;42(1):3-16.
Some (1-pyrryl)methyl derivatives of 1-ethyl-1,4-dihydro-4-oxoquinoline-3-carboxylic acid were synthetized by the standard procedure involving Gould-Jacobs and Lappin reactions. The above derivatives were tested microbiologically as nalidixic acid analogs and compared with some clinically useful 4-oxopyridine-3-carboxylic acids (nalidixic acid, pipemidic acid, norfloxacin, enoxacin and ciprofloxacin). Their antibacterial activities were very weak.
通过涉及古尔德-雅各布斯反应和拉平反应的标准程序合成了1-乙基-1,4-二氢-4-氧代喹啉-3-羧酸的一些(1-吡咯基)甲基衍生物。上述衍生物作为萘啶酸类似物进行了微生物学测试,并与一些临床上有用的4-氧代吡啶-3-羧酸(萘啶酸、吡哌酸、诺氟沙星、依诺沙星和环丙沙星)进行了比较。它们的抗菌活性非常弱。