메뉴 건너뛰기




Volumn 10, Issue 1, 2004, Pages 19-24

A convenient route to 1,4-dihydro-3-cyano-10-methyl-pyrido[3,2-g]-quinoline derivatives as key-intermediates for the synthesis of novel MDR reversal agents

Author keywords

[No Author keywords available]

Indexed keywords

1,4 DIHYDRO 3 CYANO 10 METHYLPYRIDO[3,2 G]QUINOLIN 4 ONE; 1,4 DIHYDRO 3 CYANO 10 METHYLPYRIDO[3,2 G]QUINOLIN 4 THIONE; 4 CHLORO 3 CYANO 10 METHYLPYRIDO[3,2 G]QUINOLIN 4 THIONE; ETHYL(ETHOXYMETHYLENE)CYANOACETATE; QUINOLINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 3042793169     PISSN: 07930283     EISSN: None     Source Type: Journal    
DOI: 10.1515/HC.2004.10.1.19     Document Type: Article
Times cited : (2)

References (8)
  • 1
    • 0029971845 scopus 로고    scopus 로고
    • Multidrug resistance in enteric and other Gram- negative bacteria
    • George, A.M. Multidrug resistance in enteric and other Gram- negative bacteria. FEMS Microbiol. Lett. 1996, 139, 1-10.
    • (1996) FEMS Microbiol. Lett. , vol.139 , pp. 1-10
    • George, A.M.1
  • 2
    • 0029845913 scopus 로고    scopus 로고
    • Multidrug efflux pumps of Gram-negative bacteria
    • Nikhaido, H. Multidrug efflux pumps of Gram-negative bacteria. J. Bacteriol. 1996, 178, 5853-5859.
    • (1996) J. Bacteriol. , vol.178 , pp. 5853-5859
    • Nikhaido, H.1
  • 3
    • 0029783935 scopus 로고    scopus 로고
    • Epidemiological study of an outbreak due to multidrug resistant Enterobacter aerogenes in a medical intensive care unit
    • Arpin, C.; Coze, C.; Rogues, A.M.; Gachie, J.P.; Bebear, C.; Quentin, C. Epidemiological study of an outbreak due to multidrug resistant Enterobacter aerogenes in a medical intensive care unit. J. Clin. Microbiol. 1996, 34, 2163-2169.
    • (1996) J. Clin. Microbiol. , vol.34 , pp. 2163-2169
    • Arpin, C.1    Coze, C.2    Rogues, A.M.3    Gachie, J.P.4    Bebear, C.5    Quentin, C.6
  • 4
    • 84986516337 scopus 로고
    • The synthesis of pyridoquinolines with di-alkylaminopropylamine side chains
    • Molock F., Boykin D.W. The synthesis of pyridoquinolines with di-alkylaminopropylamine side chains. J. Heterocycl. Chem. 1983, 20, 681-686.
    • (1983) J. Heterocycl. Chem. , vol.20 , pp. 681-686
    • Molock, F.1    Boykin, D.W.2
  • 5
    • 0001128013 scopus 로고    scopus 로고
    • Synthesis and antimalarial activity of new 4,6-dialkoxy and 4,6-bis(alkylthio)pyrido[3,2-g]quinoline derivatives
    • Matias C., Mahamoud A., Barbe J., Pradines B., Doury J.C. Synthesis and antimalarial activity of new 4,6-dialkoxy and 4,6-bis(alkylthio)pyrido[3,2-g] quinoline derivatives. Heterocycles 1996, 43, 1621-1632.
    • (1996) Heterocycles , vol.43 , pp. 1621-1632
    • Matias, C.1    Mahamoud, A.2    Barbe, J.3    Pradines, B.4    Doury, J.C.5
  • 6
    • 0035829416 scopus 로고    scopus 로고
    • New pyridoquinoline derivatives as potential inhibitors of the fluoroquinolone efflux pump in resistant Enterobacter aerogenes strains
    • Chevalier J., Atifi S., Eyraud A., Mahamoud A., Barbe J., Pages J.M. New pyridoquinoline derivatives as potential inhibitors of the fluoroquinolone efflux pump in resistant Enterobacter aerogenes strains. J. Med. Chem. 2001, 44, 4023-4026.
    • (2001) J. Med. Chem. , vol.44 , pp. 4023-4026
    • Chevalier, J.1    Atifi, S.2    Eyraud, A.3    Mahamoud, A.4    Barbe, J.5    Pages, J.M.6
  • 7
    • 3042840475 scopus 로고
    • Über derivate der toluylendiamincarbonsäure; m-amino-o-methylchinolin
    • Marckwald W. Über derivate der toluylendiamincarbonsäure; m-amino-o-methylchinolin. Ann. Chem. 1893, 274, 360.
    • (1893) Ann. Chem. , vol.274 , pp. 360
    • Marckwald, W.1
  • 8
    • 0010253712 scopus 로고
    • Synthesen neuer chinolon-chemotherapeutika. 1. Mitt.: Pyridochinoline und pyridophenanthroline als "lin-benzo-nalidixinsäure"-derivate
    • Jordis U., Sauter F., Rudolf M., Cai G., Synthesen neuer chinolon-chemotherapeutika. 1. Mitt.: Pyridochinoline und pyridophenanthroline als "lin-benzo-nalidixinsäure"-derivate. Monatsch. Chem. 1988, 119, 761-780.
    • (1988) Monatsch. Chem. , vol.119 , pp. 761-780
    • Jordis, U.1    Sauter, F.2    Rudolf, M.3    Cai, G.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.