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Volumn 4, Issue 4, 2007, Pages 293-296

Target-oriented synthesis of antiparasitic 2-hetaryl substituted quinolines based on imino Diels-Alder reactions

Author keywords

2 hetarylquinolines; Antiparasitic activities; Drug discovery; Leishmania chagasi; Target oriented synthesis; Trypanosoma cruzi

Indexed keywords

2 (BETA PYRIDINYL)QUINOLINE; 2 PHENYLQUINOLINE; 4 METHYL 2 ISOPROPYL (4 PYRIDINYL)QUINOLINE; 4 METHYL 8 ISOPROPYL 2 (3 PYRIDINYL)QUINOLINE; AMPHOTERICIN B; ANTIPARASITIC AGENT; NIFURTIMOX; QUINOLINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 34248172806     PISSN: 15701808     EISSN: None     Source Type: Journal    
DOI: 10.2174/157018007784620031     Document Type: Article
Times cited : (35)

References (18)
  • 7
    • 14744267865 scopus 로고    scopus 로고
    • Tempone, A.G.; Melo Pompeu da Silva, A.C.; Brandt, C.A.; Scalzaretto Martinez, F.; Treiger Borborema, S.E.; Baratada da Silveira, M.A.; Andrade Jr, H.F. Antimicrob. Agents. Chemother., 2005, 49, 1076;
    • (e) Tempone, A.G.; Melo Pompeu da Silva, A.C.; Brandt, C.A.; Scalzaretto Martinez, F.; Treiger Borborema, S.E.; Baratada da Silveira, M.A.; Andrade Jr, H.F. Antimicrob. Agents. Chemother., 2005, 49, 1076;
  • 17
    • 0036150927 scopus 로고    scopus 로고
    • For Leishmania assays, see: Escobar P.; Matu S.; Marques C.; Croft S.L. Acta Trop., 2002, 81, 151.
    • For Leishmania assays, see: Escobar P.; Matu S.; Marques C.; Croft S.L. Acta Trop., 2002, 81, 151.
  • 18
    • 0021061819 scopus 로고    scopus 로고
    • 2-95% air mixture at 37°C. After 24 h infected cultures were incubated with the compounds in a 3-fold dilution series in triplicate at each concentration for 72 h. Drug activity was determined from the % of infected cells in treated and untreated cultures in methanol fixed and Giemsa stained preparations. For mammalian cell toxicity: Vero cells or transformed THP-1 cells were incubated with the compound as above and the cell toxicity was analysed followed the MTT [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide] reduction assay described by Mosmann, T. J. Immunol. Methods, 1983, 65, 55.
    • 2-95% air mixture at 37°C. After 24 h infected cultures were incubated with the compounds in a 3-fold dilution series in triplicate at each concentration for 72 h. Drug activity was determined from the % of infected cells in treated and untreated cultures in methanol fixed and Giemsa stained preparations. For mammalian cell toxicity: Vero cells or transformed THP-1 cells were incubated with the compound as above and the cell toxicity was analysed followed the MTT [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide] reduction assay described by Mosmann, T. J. Immunol. Methods, 1983, 65, 55.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.