Journal of Natural Products · 2008 · 73 citations · 18 references
Four new meroterpenes, alisiaquinones A-C (1-3) and alisiaquinol (4), were isolated from a New Caledonian deep water sponge. Their structures and relative stereochemistry were elucidated by spectroscopic data analysis. They are related to xestoquinone, but showed unusual substitution on a tetrahydrofuran junction. They displayed micromolar range activity on two enzymatic targets of importance for the control of malaria, the plasmodial kinase Pfnek-1 and a protein farnesyl transferase, as well as on different chloroquine-sensitive and -resistant strains of Plasmodium falciparum. Alisiaquinone C displayed a submicromolar activity on P. falciparum and a competitive selectivity index on the different plasmodial strains.
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Human Malaria Parasites in Continuous Culture
William Trager, James B. Jensen · Science · 1976 · 7.9K citations
Quantitative assessment of antimalarial activity in vitro by a semiautomated microdilution technique
R. E. Desjardins, Craig J. Canfield, J. David Haynes et al. · Antimicrobial Agents and Chemotherapy · 1979 · 2.5K citations · Full text
Medicinal Chemistry, Drug Analysis, Cross-resistance Potential +15
Claudio Cassino, Giorgio Cavigiolio, Donato Colangelo et al. · Journal of Medicinal Chemistry · 2002 · 181 citations