ANIMAL CELL;
ANIMAL EXPERIMENT;
ANIMAL MODEL;
ANTIMALARIAL ACTIVITY;
ANTIPROTOZOAL ACTIVITY;
ARTICLE;
CHEMICAL MODIFICATION;
CONTROLLED STUDY;
DRUG CYTOTOXICITY;
DRUG EFFICACY;
DRUG POTENCY;
DRUG RESEARCH;
DRUG SCREENING;
DRUG SELECTIVITY;
DRUG STRUCTURE;
DRUG SYNTHESIS;
FEMALE;
IC 50;
IN VITRO STUDY;
IN VIVO STUDY;
LEISHMANIA DONOVANI;
LIPOPHILICITY;
MOUSE;
NONHUMAN;
OXIDATION;
PLASMODIUM BERGHEI INFECTION;
PLASMODIUM FALCIPARUM;
STRUCTURE ACTIVITY RELATION;
SURVIVAL TIME;
TRYPANOSOMA BRUCEI;
TRYPANOSOMA CRUZI;
TRYPANOSOMA RHODESIENSE;
How can natural products serve as a viable source of lead compounds for the development of new/novel anti-malarials?
Guantai, E.; Chibale, K. How can natural products serve as a viable source of lead compounds for the development of new/novel anti-malarials? Malar. J. 2011, 10 (Suppl. 1), S2.
Artemisinin resistance: Current status and scenarios for containment
Dondorp, A.M.; Yeung, S.; White, L.; Nguon, C; Day, N.P.J.; Socheat, D.; von Seidlein, L. Artemisinin resistance: Current status and scenarios for containment. Nat. Rev. Microbiol. 2010, 8, 272-280.
Inhibitory activity of marine sponge-derived natural products against parasitic protozoa
Orhan, I.; Şener, B.; Kaiser, M.; Brun, R.; Tasdemir, D. Inhibitory activity of marine sponge-derived natural products against parasitic protozoa. Mar. Drugs 2010, 8, 47-58.
The structural diversity and promise of antiparasitic invertebrate-derived small molecules
Watts, K.R.; Tenney, K.; Crews, P. The structural diversity and promise of antiparasitic invertebrate-derived small molecules. Curr. Opin. Biotechnol. 2010, 21, 808-818.
Synthesis and antimalarial and antituberculosis activities of a series of natural and unnatural 4-methoxy-6-styryl-pyran-2-ones, dihydro analogues and photo-dimers
McCracken, S.T.; Kaiser, M.; Boshoff, H.I.; Boyd, P.D.W.; Copp, B.R. Synthesis and antimalarial and antituberculosis activities of a series of natural and unnatural 4-methoxy-6-styryl-pyran-2-ones, Dihydro analogues and photo-dimers. Bioorg. Med. Chem. 2012, 20, 1482-1493.
Antimalarial β-carbolines from the New Zealand ascidian pseudodistoma opacum
Chan, S.T.S.; Pearce, A.N.; Page, M.J.; Kaiser, M.; Copp, B.R. Antimalarial β-carbolines from the New Zealand ascidian Pseudodistoma opacum. J. Nat. Prod. 2011, 74, 1972-1979.
Chemical and biological explorations of the electrophilic reactivity of the bioactive marine natural product halenaquinone with biomimetic nucleophiles
Wang, J.; Bourguet-Kondracki, M.-L.; Longeon, A.; Dubois, J.; Valentin, A.; Copp, B.R. Chemical and biological explorations of the electrophilic reactivity of the bioactive marine natural product halenaquinone with biomimetic nucleophiles. Bioorg. Med. Chem. Lett. 2011, 21, 1261-1264.
Orthidines A-E, tubastrine, 3,4-dimethoxyphenethyl-β-guanidine, and 1,14-sperminedihomovanillamide: Potential anti-inflammatory alkaloids isolated from the New Zealand ascidian aplidium orthium that act as inhibitors of neutrophil respiratory burst
Pearce, A.N.; Chia, E.W.; Berridge, M.V.; Maas, E.W.; Page, M.J.; Harper, J.L.; Webb, V.L.; Copp, B.R. Orthidines A-E, tubastrine, 3,4- dimethoxyphenethyl-β-guanidine, and 1,14-sperminedihomovanillamide: potential anti-inflammatory alkaloids isolated from the New Zealand ascidian Aplidium orthium that act as inhibitors of neutrophil respiratory burst. Tetrahedron 2008, 64, 5748-5755.
Discovery and preliminary structure-activity relationship analysis of 1,14-sperminediphenylacetamides as potent and selective antimalarial lead compounds
Liew, L.P.P.; Kaiser, M.; Copp, B.R. Discovery and preliminary structure-activity relationship analysis of 1,14-sperminediphenylacetamides as potent and selective antimalarial lead compounds. Bioorg. Med. Chem. Lett. 2013, 23, 452-454.
Synthesis and in vitro and in vivo evaluation of antimalarial polyamines
Liew, L.P.P.; Pearce, A.N.; Kaiser, M.; Copp, B.R. Synthesis and in vitro and in vivo evaluation of antimalarial polyamines. Eur. J. Med. Chem. 2013, 69, 22-31.
Anti-inflammatory thiazine alkaloids isolated from the New Zealand ascidian aplidium sp.: Inhibitors of the neutrophils respiratory burst in a model of gouty arthritis
Pearce, A.N.; Chia, E.W.; Berridge, M.V.; Clark, G.R.; Harper, J.L.; Larsen, L.; Maas, E.W.; Page, M.J.; Perry, N.B.; Webb, V.L.; et al. Anti-inflammatory thiazine alkaloids isolated from the New Zealand ascidian Aplidium sp.: Inhibitors of the neutrophils respiratory burst in a model of gouty arthritis. J. Nat. Prod. 2007, 70, 936-940.
Biomimetic synthesis of the apoptosis-inducing thiazinoquinone thiaplidiaquinone A
Carbone, A.; Lucas, C.L.; Moody, C.J. Biomimetic synthesis of the apoptosis-inducing thiazinoquinone thiaplidiaquinone A. J. Org. Chem. 2012, 77, 9179-9189.
A plasmodium berghei reference line that constitutively expresses GFP at a high level throughout the complete life cycle
Franke-Fayard, B.; Trueman, H.; Ramesar, J.; Mendoza, J.; van der Keur, M.; van der Linden, R.; Sinden, R.E.; Waters, A.P.; Janse, C.J. A Plasmodium berghei reference line that constitutively expresses GFP at a high level throughout the complete life cycle. Mol. Biochem. Parasitol. 2004, 137, 23-33.