Antimicrobial quinolone thioureas

作者: Ronald Eugene White , Thomas Prosser Demuth

DOI:

关键词:

摘要: Antimicrobial quinolone thiourea compounds of general formula (I), wherein (1) A?1, A2, A3, R1, R3, R4, and R6? form any a variety related heterocyclic structures similar to those known in the art have antimicrobial activity; (2) R1 is X, R3 or both R?1 R3? are X; X -R?15-N(R16)(R17) -R15-R18-N(R19)(R17?), where (a) R15 nil, alkyl, carbocyclic ring, ring; R16 hydrogen; alkyl; alkenyl; (3) when R?15-N(R16)(R17), R15? may together comprise ring including nitrogen atom which R?15 R16? bonded; (b) R17 C(=S)-NR20R21; R20 hydrogen, alkenyl, R?21 N(R20)(R20); R21?, with they bonded, (c) R18) R19 R?18 R19? pharmaceutically-acceptable salts biohydrolyzable esters thereof, hydrates thereof.

参考文章(45)
Hans-Joachim Zeiler, Karl G. Metzger, Klaus Grohe, 6-fluoro-7-chloro-1-cyclopropyl-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid ,(1985)
Michiyuki Sendai, Mitsumi Tomimoto, Matsuo Taisuke, Shoji Kishimoto, Ochiai Michihiko, 1-sulfo-2-oxoazetidine derivatives, their production and use ,(1981)
S Mobashery, M Johnston, Reactions of Escherichia coli TEM beta-lactamase with cephalothin and with C10-dipeptidyl cephalosporin esters. Journal of Biological Chemistry. ,vol. 261, pp. 7879- 7887 ,(1986) , 10.1016/S0021-9258(19)57485-3
Ronald Eugene White, Thomas Prosser Demuth, Antimicrobial quinolonyl lactams ,(1991)
J S Wolfson, D C Hooper, The fluoroquinolones: structures, mechanisms of action and resistance, and spectra of activity in vitro. Antimicrobial Agents and Chemotherapy. ,vol. 28, pp. 581- 586 ,(1985) , 10.1128/AAC.28.4.581
Shahriar. Mobashery, Stephen A. Lerner, Michael. Johnston, Conscripting β-Lactamase for Use in Drug Delivery. Synthesis and Biological Activity of a Cephalosporin C10-Ester of an Antibiotic Dipeptide. Journal of the American Chemical Society. ,vol. 108, pp. 1685- 1686 ,(1986) , 10.1021/JA00267A045
J G Christenson, K K Chan, R Cleeland, B Dix-Holzknecht, H H Farrish, I H Patel, A Specian, Pharmacokinetics of Ro 23-9424, a dual-action cephalosporin, in animals Antimicrobial Agents and Chemotherapy. ,vol. 34, pp. 1895- 1900 ,(1990) , 10.1128/AAC.34.10.1895
Hiroshi Egawa, Teruyuki Miyamoto, Akira Minamida, Yoshiro Nishimura, Hidetsugu Okada, Hitoshi Uno, Junichi Matsumoto, Pyridonecarboxylic acids as antibacterial agents. 4. Synthesis and antibacterial activity of 7-(3-amino-1-pyrrolidinyl)-1-ethyl-6-fluoro-1,4 -dihydro-4-oxo-1,8-naphthyridine-3-carboxylic acid and its analogues. Journal of Medicinal Chemistry. ,vol. 27, pp. 1543- 1548 ,(1984) , 10.1021/JM00378A004
C. H. O'Callaghan, R. B. Sykes, S. E. Staniforth, A new cephalosporin with a dual mode of action. Antimicrobial Agents and Chemotherapy. ,vol. 10, pp. 245- 248 ,(1976) , 10.1128/AAC.10.2.245