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Volumn 19, Issue 7, 2009, Pages 2033-2037

Antitumour and antimalarial activity of artemisinin-acridine hybrids

Author keywords

Acridine; Anticancer; Antimalarial; Apoptosis; Artemisinin; Confocal microscopy; DNA

Indexed keywords

ACRIDINE; ARTEMETHER; ARTEMISININ; ARTEMISININ ACRIDINE; CHLOROQUINE; DIHYDROARTEMISININ; UNCLASSIFIED DRUG;

EID: 62149130062     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2009.02.028     Document Type: Article
Times cited : (62)

References (31)
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    • note
    • 6: C, 64.96; H, 6.61; N, 6.89. Found: C, 65.00; H, 6.78; N, 6.93.
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    • note
    • 50 values were calculated from individual inhibition curves plotted by Grafit software. The same method was used to determine cytotoxicity against HT29-AK and MDA-MB-231 cells at drug concentrations up to 750 μM.
  • 22
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    • For in vitro antimalarial assessment versus the 3D7 strain of Plasmodium falciparum the following protocol was employed. Parasites were maintained in continuous culture using the method of Jensen and Trager:
    • For in vitro antimalarial assessment versus the 3D7 strain of Plasmodium falciparum the following protocol was employed. Parasites were maintained in continuous culture using the method of Jensen and Trager:. Trager W., and Jensen J.B. Science 193 (1976) 673-675
    • (1976) Science , vol.193 , pp. 673-675
    • Trager, W.1    Jensen, J.B.2
  • 23
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    • Antimalarial activity was assessed with an adaption of the 48 hr sensitivity assay of Desjardins et al. using [3H]-hypoxanthine incorporation as an assessment of parasite growth:
    • Antimalarial activity was assessed with an adaption of the 48 hr sensitivity assay of Desjardins et al. using [3H]-hypoxanthine incorporation as an assessment of parasite growth:. Desjardins R.E., Canfield C.J., Haynes J.D., Chulay J.D. Antimicrob. Agents Chemother. 16 (1979) 710-718
    • (1979) Antimicrob. Agents Chemother. , vol.16 , pp. 710-718
    • Desjardins, R.E.1    Canfield, C.J.2    Haynes, J.D.3    Chulay, J.D.4
  • 24
    • 62149093250 scopus 로고    scopus 로고
    • note
    • 5 cells) were washed in HBSS and the resultant cell pellet was resuspended in 500 μL of TMRE solution (50 nM in HBSS) and incubated for 10 min at 37 °C. A minimum of 500 cells were measured by flow cytometry on fluorescence channel FL-2 (Coulter Epics, XL Software). The data was analysed using WinMDI, v2.8 software (Scripps Institute, California, USA).
  • 25
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    • note
    • 6) were washed twice in HBSS, fixed in 1 mL of ice-cold 70% ethanol, and frozen at -20 °C. After 2 h the 70% ethanol was removed and the cell pellet was resuspended in 1 mL of PI stock solution (phosphate-buffered saline containing 40 μg/mL PI, 0.1 mg/mL RNase, and 3.8 mM sodium citrate)) and incubated at 37 °C (30 min). A minimum of 5000 cells were analysed by flow cytometry. PI fluorescence was measured on fluorescence channel FL-2. The proportion of cells in each stage of the cell cycle was calculated from the DNA content of the cell using WinMDI, v2.8 software.
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    • note
    • 29
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    • In Drug-Nuc
    • Chaires, J.B, Waring, M.J, Eds, Academic Press: London
    • Eriksson, M.; Norden, B. In Drug-Nuc. Acid Int.; Chaires, J.B., Waring, M.J., Eds.; Academic Press: London, 2001; Vol. 340, p 68.
    • (2001) Acid Int , vol.340 , pp. 68
    • Eriksson, M.1    Norden, B.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.