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Journal Abstract Search

163 related items for PubMed ID: 8582014

  • 1. Imidazo- and triazoloquinolones as antibacterial agents. Synthesis and structure-activity relationships.
    Fujita M, Egawa H, Kataoka M, Miyamoto T, Nakano J, Matsumoto J.
    Chem Pharm Bull (Tokyo); 1995 Dec; 43(12):2123-32. PubMed ID: 8582014
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  • 2. Fluorocyclopropyl quinolones. 1. Synthesis and structure-activity relationships of 1-(2-fluorocyclopropyl)-3-pyridonecarboxylic acid antibacterial agents.
    Atarashi S, Imamura M, Kimura Y, Yoshida A, Hayakawa I.
    J Med Chem; 1993 Oct 29; 36(22):3444-8. PubMed ID: 8230135
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  • 3. 1,2,3-triazolo[4,5-h]quinolines. III. Preparation and antimicrobial evaluation of 4-ethyl-4,7-dihydro-1(2)-R-1(2)H triazolo[4,5-h]quinolin-7-one-6-carboxylic acids as anti-infectives of the urinary tract.
    Sanna P, Carta A, Paglietti G, Zanetti S, Fadda G.
    Farmaco; 1992 Oct 29; 47(7-8):1001-19. PubMed ID: 1332728
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  • 4. The synthesis and antibacterial activities of quinolones containing five- and six-membered heterocyclic substituents at the 7-position.
    Cooper CS, Klock PL, Chu DT, Fernandes PB.
    J Med Chem; 1990 Apr 29; 33(4):1246-52. PubMed ID: 2319566
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  • 5. Studies on quinolone antibacterials. IV. Structure-activity relationships of antibacterial activity and side effects for 5- or 8-substituted and 5,8-disubstituted-7-(3-amino-1-pyrrolidinyl)-1-cyclopropyl-1, 4-dihydro-4-oxoquinoline-3-carboxylic acids.
    Yoshida T, Yamamoto Y, Orita H, Kakiuchi M, Takahashi Y, Itakura M, Kado N, Mitani K, Yasuda S, Kato H, Itoh Y.
    Chem Pharm Bull (Tokyo); 1996 May 29; 44(5):1074-85. PubMed ID: 8689718
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  • 7. Synthesis and antibacterial activity of new tetracyclic quinolone antibacterials.
    Taguchi M, Kondo H, Inoue Y, Kawahata Y, Jinbo Y, Sakamoto F, Tsukamoto G.
    J Med Chem; 1992 Jan 29; 35(1):94-9. PubMed ID: 1310116
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  • 9. 1,2,3-triazolo[4,5-f]quinolines. II. Preparation and antimicrobial evaluation of 6-ethyl-6,9-dihydro-1(2)(3)-R-1(2) (3)H-triazolo [4,5-f]quinolin-9-one-8-carboxylic acids as anti-infectives of the urinary tract (1).
    Nuvole A, Sanna P, Paglietti G, Juliano C, Zanetti S, Cappuccinelli P.
    Farmaco; 1989 Jun 29; 44(6):619-32. PubMed ID: 2553038
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  • 10. Synthesis and biological activity of 5-alkyl-1,7,8-trisubstituted-6-fluoroquinoline-3-carboxylic acids.
    Hagen SE, Domagala JM, Heifetz CL, Johnson J.
    J Med Chem; 1991 Mar 29; 34(3):1155-61. PubMed ID: 2002456
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  • 12. Synthesis and evaluation of antibacterial activity of 7-alkyloxy-4,5-dihydro-imidazo[1,2-a]quinoline derivatives.
    Sun XY, Wu R, Wen X, Guo L, Zhou CP, Li J, Quan ZS, Bao J.
    Eur J Med Chem; 2013 Feb 29; 60():451-5. PubMed ID: 23321259
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  • 15. [Studies on pyridonecarboxylic acids as antibacterial agents. XIV. Synthesis and structure-activity relationships of 7,8-disubstituted-1-cyclopropyl-6-methyl-1,4-dihydro-4-oxo-3-quinoline carboxylic acids].
    Wang H, Qi J, Sun L, Yu L, Guo H.
    Yao Xue Xue Bao; 1998 Sep 29; 33(9):675-81. PubMed ID: 12016871
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  • 16. Synthesis and antibacterial activity of novel 6-fluoro-1-[(1R,2S)-2-fluorocyclopropan-1-yl]-4-oxoquinoline-3-carboxylic acids bearing cyclopropane-fused 2-amino-8-azabicyclo[4.3.0]nonan-8-yl substituents at the C-7 position.
    Inagaki H, Takahashi H, Takemura M.
    Bioorg Med Chem Lett; 2004 Oct 18; 14(20):5193-8. PubMed ID: 15380226
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  • 17. 6-Aminoquinolones: a new class of quinolone antibacterials?
    Cecchetti V, Clementi S, Cruciani G, Fravolini A, Pagella PG, Savino A, Tabarrini O.
    J Med Chem; 1995 Mar 17; 38(6):973-82. PubMed ID: 7699714
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  • 18. Synthesis and structure elucidation of some 4-substituted benzylidene amino-5-[3(5)-methyl-5(3)-phenyl-1H-1-pyrazolyl]-2,4-dihydro-3H-1,2,4- triazole-3-thione derivatives with their antimicrobial activities.
    Doğan HN, Büyüktimkin S, Rollas S, Yemni E, Cevikbaş A.
    Farmaco; 1997 Mar 17; 52(8-9):565-8. PubMed ID: 9507666
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  • 20. Fluoronaphthyridines as antibacterial agents. 6. Synthesis and structure-activity relationships of new chiral 7-(1-, 3-, 4-, and 6-methyl-2,5-diazabicyclo[2.2.1]heptan-2-yl)naphthyridine analogues of 7-[(1R,4R)-2,5- diazabicyclo[2.2.1]heptan-2-yl]-1-(1,1-dimethylethyl)-6-fluoro-1,4-dihy dro-4-oxo-1,8-naphthyridine-3-carboxylic acid. Influence of the configuration on blood pressure in dogs. A quinolone-class effect.
    Remuzon P, Bouzard D, Guiol C, Jacquet JP.
    J Med Chem; 1992 Jul 24; 35(15):2898-909. PubMed ID: 1322990
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