about
Artemisinin and a Series of Novel Endoperoxide Antimalarials Exert Early Effects on Digestive Vacuole MorphologyIdentification of an antimalarial synthetic trioxolane drug development candidateRedox-directed cancer therapeutics: molecular mechanisms and opportunitiesEndoperoxide antimalarials: development, structural diversity and pharmacodynamic aspects with reference to 1,2,4-trioxane-based structural scaffoldParallel synthesis of 9-aminoacridines and their evaluation against chloroquine-resistant Plasmodium falciparumSynthesis and antimalarial activity of metal complexes of cross-bridged tetraazamacrocyclic ligands.Nox4-dependent ROS modulation by amino endoperoxides to induce apoptosis in cancer cellsSynthetic ozonide drug candidate OZ439 offers new hope for a single-dose cure of uncomplicated malaria.Mycangimycin, a polyene peroxide from a mutualist Streptomyces spThe therapeutic potential of semi-synthetic artemisinin and synthetic endoperoxide antimalarial agents.Monoclonal Antibodies That Recognize the Alkylation Signature of Antimalarial Ozonides OZ277 (Arterolane) and OZ439 (Artefenomel).The antimalarial trioxaquine DU1301 alkylates heme in malaria-infected mice.Preparation of bicyclic 1,2,4-trioxanes from gamma,delta-unsaturated ketonesIn vitro activity of anti-malarial ozonides against an artemisinin-resistant isolate.Tetraoxanes: synthetic and medicinal chemistry perspective.Bacterial symbionts in agricultural systems provide a strategic source for antibiotic discovery.Synthesis of five- and six-membered cyclic organic peroxides: Key transformations into peroxide ring-retaining products.A single, low, oral dose of a 5-carbon-linked trioxane dimer orthoester plus mefloquine cures malaria-infected mice.Antimalarial Preclinical Drug Development: A Single Oral Dose of A 5-Carbon-linked Trioxane Dimer Plus Mefloquine Cures Malaria-Infected Mice.Malaria-Infected Mice Are Cured by a Single Low Dose of a New Silylamide Trioxane Plus Mefloquine.Navigating the Chiral Pool in the Total Synthesis of Complex Terpene Natural Products.Use of Integrated Computational Approaches in the Search for New Therapeutic Agents.Probing the antimalarial mechanism of artemisinin and OZ277 (arterolane) with nonperoxidic isosteres and nitroxyl radicals.Peroxide bond-dependent antiplasmodial specificity of artemisinin and OZ277 (RBx11160).An asymmetric synthesis of 1,2,4-trioxane anticancer agents via desymmetrization of peroxyquinols through a Brønsted acid catalysis cascade.Evidence for a common non-heme chelatable-iron-dependent activation mechanism for semisynthetic and synthetic endoperoxide antimalarial drugs.Probing the Peroxycarbenium [3+2] Cycloaddition Reactions with 1,2-Disubstituted Ethylenes: Results and Insights.Synthesis and antimalarial activity of 3,3-spiroanellated 5,6-disubstituted 1,2,4-trioxanes.Malaria-infected mice are cured by a single oral dose of new dimeric trioxane sulfones which are also selectively and powerfully cytotoxic to cancer cells.Comparison of the Exposure Time Dependence of the Activities of Synthetic Ozonide Antimalarials and Dihydroartemisinin against K13 Wild-Type and Mutant Plasmodium falciparum Strains.Relationship between antimalarial activity and heme alkylation for spiro- and dispiro-1,2,4-trioxolane antimalarials.Potent antimalarial 1,2,4-trioxanes through perhydrolysis of epoxides.Simple analogues of qinghaosu (artemisinin).Comparative antimalarial activities of six pairs of 1,2,4,5-tetraoxanes (peroxide dimers) and 1,2,4,5,7,8-hexaoxonanes (peroxide trimers).5-Bromo-spiro-[1,2-dioxane-4,4'-tricyclo-[4.3.1.1]undeca-ne]-3'-ol.Four-step synthesis of the antimalarial cardamom peroxide via an oxygen stitching strategy.[3+2] Photooxygenation of aryl cylopropanes via visible light photocatalysis.Synthesis of spiroannulated and 3-arylated 1,2,4-trioxanes from mesitylol and methyl 4-hydroxytiglate by photooxygenation and peroxyacetalizationEndoperoxide synthesis by photocatalytic aerobic [2 + 2 + 2] cycloadditions3-Alkoxy-1,2-Dioxolanes: Synthesis and Evaluation as Potential Antimalarial Agents.
P2860
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P2860
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
2004年论文
@zh
2004年论文
@zh-cn
name
Synthetic peroxides as antimalarials.
@ast
Synthetic peroxides as antimalarials.
@en
type
label
Synthetic peroxides as antimalarials.
@ast
Synthetic peroxides as antimalarials.
@en
prefLabel
Synthetic peroxides as antimalarials.
@ast
Synthetic peroxides as antimalarials.
@en
P2093
P356
P1476
Synthetic peroxides as antimalarials.
@en
P2093
Jonathan L Vennerstrom
Yuanqing Tang
Yuxiang Dong
P304
P356
10.1002/MED.10066
P577
2004-07-01T00:00:00Z