메뉴 건너뛰기




Volumn 19, Issue 8, 2009, Pages 2360-2363

Synthesis and in vitro activity of new tetrahydronaphtho[1,2-b]azepine derivatives against Trypanosoma cruzi and Leishmania chagasi parasites

Author keywords

1,4 Epoxytetrahydronaphtho 1,2 b azepines; Anti parasitic agents; Chagas' disease; Drug discovery; Leishmania chagasi; Tetrahydronaphtho 1,2 b azepines; Trypanosoma cruzi

Indexed keywords

1,4 EPOXY 2,3,4,5 TETRAHYDRONAPHTHO[1,2 B]AZEPINE DERIVATIVE; 2 (4' BROMOPHENYL) 4 HYDROXYTETRAHYDRONAPHTHO[1,2 B]AZEPINE; 3' BROMOPHENYL 1,4 EPOXYTETRAHYDRONAPHTHO[1,2 B]AZEPINE; 4 HYDROXY 2,3,4,5 TETRAHYDRONAPHTHO[1,2 B]AZEPINE DERIVATIVE; 4' CHLOROPHENYL 1,4 EPOXYTETRAHYDRONAPHTHO[1,2 B]AZEPINE; ANTIPARASITIC AGENT; TETRAHYDRONAPHTHO[1,2 B]AZEPINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 63349106395     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2008.05.013     Document Type: Article
Times cited : (46)

References (27)
  • 27
    • 0036150927 scopus 로고    scopus 로고
    • note
    • 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 percentage 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 analyzed following 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.