All Stories

  1. Design, Synthesis and Antiplasmodial Activities of a Library of Fluorine-Based 3-Benzylmenadiones
  2. Synthesis of 1,2,3‐Triazole‐Methyl‐Menadione Derivatives: Evaluation of Electrochemical and Antiparasitic Properties against two Blood‐Dwelling Parasites
  3. Click Coupling of Flavylium Dyes with Plasmodione Analogues: Towards New Redox‐Sensitive Pro‐Fluorophores
  4. Regioselective Synthesis of Potential Non-Quinonoid Prodrugs of Plasmodione: Antiparasitic Properties Against Two Hemoglobin-Feeding Parasites and Drug Metabolism Studies
  5. Chemoselective Synthesis and Anti-Kinetoplastidal Properties of 2,6-Diaryl-4H-tetrahydro-thiopyran-4-one S-Oxides: Their Interplay in a Cascade of Redox Reactions from Diarylideneacetones
  6. Synthesis and Photochemical Properties of Fluorescent Metabolites Generated from Fluorinated Benzoylmenadiones in Living Cells
  7. Evaluation of ferrocenyl-containing γ-hydroxy-γ-lactam-derived tetramates as potential antiplasmodials
  8. Efficient Multigram-Scale Synthesis of 7-Substituted 3-Methyltetral-1-ones and 6-Fluoromenadione
  9. The parasitophorous vacuole nutrient channel is critical for drug access in malaria parasites and modulates the artemisinin resistance fitness cost
  10. Bioinspired Photoredox Benzylation of Quinones
  11. Direct C−H Radical Alkylation of 1,4‐Quinones
  12. Magnesium Complexes of Ladanein: A Beneficial Strategy for Stabilizing Polyphenolic Antivirals
  13. A Class of Valuable (Pro-)Activity-Based Protein Profiling Probes: Application to the Redox-Active Antiplasmodial Agent, Plasmodione
  14. Plasmodium falciparum Ferredoxin-NADP+ Reductase-Catalyzed Redox Cycling of Plasmodione Generates Both Predicted Key Drug Metabolites: Implication for Antimalarial Drug Development
  15. Repurposing Auranofin and Evaluation of a New Gold(I) Compound for the Search of Treatment of Human and Cattle Parasitic Diseases: From Protozoa to Helminth Infections
  16. A role for the succinate dehydrogenase in the mode of action of the redox-active antimalarial drug, plasmodione
  17. A Mild and Versatile Friedel–Crafts Methodology for the Diversity‐Oriented Synthesis of Redox‐Active 3‐Benzoylmenadiones with Tuneable Redox Potentials
  18. A Mild and Versatile Friedel–Crafts Methodology for the Diversity‐Oriented Synthesis of Redox‐Active 3‐Benzoylmenadiones with Tunable Redox Potentials
  19. Antiplasmodial Activity of Nitroaromatic Compounds: Correlation with Their Reduction Potential and Inhibitory Action on Plasmodium falciparum Glutathione Reductase
  20. Investigating the mode of action of the redox-active antimalarial drug plasmodione using the yeast model
  21. Selenium Status in Elderly People: Longevity and Age-Related Diseases
  22. Author Correction: Arylmethylamino steroids as antiparasitic agents
  23. Physicochemical Properties Govern the Activity of Potent Antiviral Flavones
  24. AntiMalarial Mode of Action (AMMA) Database: Data Selection, Verification and Chemical Space Analysis
  25. Synthesis of plasmodione metabolites and13C-enriched plasmodione as chemical tools for drug metabolism investigation
  26. Iron(iii) coordination properties of ladanein, a flavone lead with a broad-spectrum antiviral activity
  27. QSAR modeling and chemical space analysis of antimalarial compounds
  28. A high susceptibility to redox imbalance of the transmissible stages of Plasmodium falciparum revealed with a luciferase‐based mature gametocyte assay
  29. Arylmethylamino steroids as antiparasitic agents
  30. Pharmacomodulation of the Antimalarial Plasmodione: Synthesis of Biaryl- and N-Arylalkylamine Analogues, Antimalarial Activities and Physicochemical Properties
  31. A Redox-Active Fluorescent pH Indicator for Detecting Plasmodium falciparum Strains with Reduced Responsiveness to Quinoline Antimalarial Drugs
  32. ChemInform Abstract: A Platform of Regioselective Methodologies to Access Polysubstituted 2-Methyl-1,4-naphthoquinone Derivatives: Scope and Limitations.
  33. In Silico Mining for Antimalarial Structure-Activity Knowledge and Discovery of Novel Antimalarial Curcuminoids
  34. The Redox Cycler Plasmodione Is a Fast-Acting Antimalarial Lead Compound with Pronounced Activity against Sexual and Early Asexual Blood-Stage Parasites
  35. A Platform of Regioselective Methodologies to Access Polysubstituted 2-Methyl-1,4-naphthoquinone Derivatives: Scope and Limitations
  36. Redox Polypharmacology as an Emerging Strategy to Combat Malarial Parasites
  37. Synthesis and evaluation of 1,4-naphthoquinone ether derivatives asSmTGR inhibitors and new anti-schistosomal drugs
  38. ChemInform Abstract: Diastereoselective Synthesis of 2,6-Diaryltetrahydrothiopyran-4-ones by Phase-Transfer Catalysis.
  39. Antimalarial NADPH-Consuming Redox-Cyclers As Superior Glucose-6-Phosphate Dehydrogenase Deficiency Copycats
  40. Diastereoselective Synthesis of 2,6-Diaryltetrahydrothiopyran-4-ones by Phase-Transfer Catalysis
  41. Electrochemical Properties of Substituted 2-Methyl-1,4-Naphthoquinones: Redox Behavior Predictions
  42. Antiglioma activity of GoPI-sugar, a novel gold(I)–phosphole inhibitor: Chemical synthesis, mechanistic studies, and effectiveness in vivo
  43. A Practical and Economical High-Yielding, Six-Step Sequence Synthesis of a Flavone: Application to the Multigram-Scale Synthesis of Ladanein
  44. Versatile Synthesis of Dissymmetric Diarylideneacetones via a Palladium-Catalyzed­ Coupling-Isomerization Reaction
  45. ChemInform Abstract: Versatile Synthesis of Dissymmetric Diarylideneacetones via a Palladium-Catalyzed Coupling-Isomerization Reaction.
  46. Redox-Active Agents in Reactions Involving the Trypanothione/Trypanothione Reductase-based System to Fight Kinetoplastidal Parasites
  47. 1,4-Naphthoquinones and Other NADPH-Dependent Glutathione Reductase- Catalyzed Redox Cyclers as Antimalarial Agents
  48. The Antimalarial Activities of Methylene Blue and the 1,4-Naphthoquinone 3-[4-(Trifluoromethyl)Benzyl]-Menadione Are Not Due to Inhibition of the Mitochondrial Electron Transport Chain
  49. Drug Discovery in Infectious Diseases, Volume 3: Parasitic Helminths: Targets, Screens, Drugs and Vaccines. Edited by Conor R. Caffrey
  50. Versatile Synthesis of Dissymmetric Diarylideneacetones via a Palladium-Catalyzed­ Coupling–Isomerization Reaction
  51. Interactions of the Antimalarial Drug Methylene Blue with Methemoglobin and Heme Targets inPlasmodium falciparum: A Physico-Biochemical Study
  52. A Plant-Derived Flavonoid Inhibits Entry of All HCV Genotypes Into Human Hepatocytes
  53. Synthesis and biological evaluation of 1,4-naphthoquinones and quinoline-5,8-diones as antimalarial and schistosomicidal agents
  54. Exploring the trifluoromenadione core as a template to design antimalarial redox-active agents interacting with glutathione reductase
  55. Glutathione Reductase-Catalyzed Cascade of Redox Reactions To Bioactivate Potent Antimalarial 1,4-Naphthoquinones – A New Strategy to Combat Malarial Parasites
  56. Subversive Substrates of Glutathione Reductases from Plasmodium falciparum-Infected Red Blood Cells as Antimalarial Agents
  57. ChemInform Abstract: New Steroidal Diazo Ketones as Potential Photoaffinity Labeling Reagents for the Mineralocorticoid Receptor: Synthesis and Biological Activities.
  58. ChemInform Abstract: New Potent Inhibitors of Trypanothione Reductase from Trypanosoma cruzi in the 2-Aminodiphenylsulfide Series.
  59. ChemInform Abstract: Structure-Activity Relationships in 2-Aminodiphenylsulfides Against Trypanothione Reductase from Trypanosoma cruzi.
  60. ChemInform Abstract: A General Approach to the Synthesis of Polyamine Linked-Monoindolylmaleimides, a New Series of Trypanothione Reductase Inhibitors.
  61. ChemInform Abstract: Automated Parallel Synthesis of a Tetrahydroisoquinolin-Based Library: Potential Prolyl Endopeptidase Inhibitors.
  62. Antimalarial versus Cytotoxic Properties of Dual Drugs Derived From 4-Aminoquinolines and Mannich Bases: Interaction with DNA
  63. 752 INHIBITION OF HEPATITS C VIRUS ENTRY BY A PLANT-DERIVED FLAVONE
  64. Antimalarial activities of ferroquine conjugates with either glutathione reductase inhibitors or glutathione depletors via a hydrolyzable amide linker
  65. Unsaturated Mannich Bases Active Against Multidrug-ResistantTrypanosoma brucei bruceiStrains
  66. A Sugar-Modified Phosphole Gold Complex with Antiproliferative Properties Acting as a Thioredoxin Reductase Inhibitor in MCF-7 Cells
  67. Antimalarial Dual Drugs Based on Potent Inhibitors of Glutathione Reductase fromPlasmodium falciparum
  68. The aza-analogues of 1,4-naphthoquinones are potent substrates and inhibitors of plasmodial thioredoxin and glutathione reductases and of human erythrocyte glutathione reductase
  69. Correction: Thioredoxin Glutathione Reductase from Schistosoma mansoni: An Essential Parasite Enzyme and a Key Drug Target
  70. Thioredoxin Glutathione Reductase from Schistosoma mansoni: An Essential Parasite Enzyme and a Key Drug Target
  71. Crystal Structure of human Glutathione Reductase complexed with a Fluoro-Analogue of the Menadione Derivative M5
  72. A Fluoro Analogue of the Menadione Derivative 6-[2‘-(3‘-Methyl)-1‘,4‘-naphthoquinolyl]hexanoic Acid Is a Suicide Substrate of Glutathione Reductase. Crystal Structure of the Alkylated Human Enzyme†
  73. Specific Inhibitors of Plasmodium falciparum Thioredoxin Reductase as Potential Antimalarial Agents.
  74. Crystal Structure Analysis of the human Glutahione Reductase, complexed with GoPI
  75. Specific inhibitors of Plasmodium falciparum thioredoxin reductase as potential antimalarial agents
  76. Gold(I)-Phosphinkomplexe für die irreversible Hemmung von humanen Disulfid-Reduktasen
  77. Undressing of Phosphine Gold(I) Complexes as Irreversible Inhibitors of Human Disulfide Reductases
  78. Irreversible Inactivation of Trypanothione Reductase by Unsaturated Mannich Bases:  A Divinyl Ketone as Key Intermediate
  79. Synthesis of 5-Nitro-2-furancarbohydrazides and Theircis-Diamminedichloroplatinum Complexes as Bitopic and Irreversible Human Thioredoxin Reductase Inhibitors
  80. Mechanistic Studies on a Novel, Highly Potent Gold-Phosphole Inhibitor of Human Glutathione Reductase
  81. 5-Substituted Tetrazoles as Bioisosteres of Carboxylic Acids. Bioisosterism and Mechanistic Studies on Glutathione Reductase Inhibitors as Antimalarials
  82. Screening of Plasmodium falciparum iron superoxide dismutase inhibitors and accuracy of the SOD-assays
  83. Mechanism-Based Inactivation of Thioredoxin Reductase fromPlasmodium falciparumby Mannich Bases. Implication for Cytotoxicity†
  84. Double-drug development against antioxidant enzymes fromPlasmodium falciparum
  85. Antitrypanosomal Activities and Cytotoxicity of 5-Nitro-2-furancarbohydrazides.
  86. A novel mechanism for inhibition of HIV-1 reverse transcriptase
  87. Antitrypanosomal activities and cytotoxicity of 5-nitro-2-furancarbohydrazides
  88. Comparison of the Inhibition of Human and Trypanosoma cruzi Prolyl Endopeptidases
  89. A Prodrug Form of aPlasmodium falciparumGlutathione Reductase Inhibitor Conjugated with a 4-Anilinoquinoline
  90. Trypanosoma cruzi Prolyl Oligopeptidase Tc80 Is Involved in Nonphagocytic Mammalian Cell Invasion by Trypomastigotes
  91. Bromination Studies of the 2,3-Dimethylnaphthazarin Core Allowing Easy Access to Naphthazarin Derivatives
  92. Antiplasmodial Activity and Cytotoxicity of Bis-, Tris-, and Tetraquinolines with Linear or Cyclic Amino Linkers
  93. Potent and specific inhibitors of trypanothione reductase from Trypanosoma cruzi
  94. 2- and 3-Substituted 1,4-Naphthoquinone Derivatives as Subversive Substrates of Trypanothione Reductase and Lipoamide Dehydrogenase fromTrypanosomacruzi:  Synthesis and Correlation between Redox Cycling Activities and in Vitro Cytotoxicity
  95. The conserved redox-sensitive cysteine residue of the DNA-binding region in the c-Rel protein is involved in the regulation of the phosphorylation of the protein
  96. The conserved redox-sensitive cysteine residue of the DNA-binding region in the c-Rel protein is involved in the regulation of the phosphorylation of the protein
  97. Antimalarial, Antitrypanosomal, and Antileishmanial Activities and Cytotoxicity of Bis(9-amino-6-chloro-2-methoxyacridines):  Influence of the Linker#
  98. Parallel synthesis of a library of 1,4-naphthoquinones and automated screening of potential inhibitors of trypanothione reductase from Trypanosoma cruzi
  99. Trypanothione reductase inhibition/trypanocidal activity relationships in a 1,4-bis(3-aminopropyl)piperazine series
  100. Synthesis of polyamine derivatives for the preparation of affinity chromatography columns for the search of new Trypanosoma cruzi targets
  101. Synthesis of 5,5′-Dithiobis(2-nitrobenzamides)as Alternative Substrates for Trypanothione Reductase and Thioredoxin Reductase: A Microtiter Colorimetric Assay for Inhibitor Screening
  102. Automated parallel synthesis of a tetrahydroisoquinolin-based library: Potential prolyl endopeptidase inhibitors
  103. Evidence for the co-existence of glutathione reductase and trypanothione reductase in the non-trypanosomatid Euglenozoa: Euglena gracilis Z
  104. 18-Vinyldeoxycorticosterone: a potent inhibitor of the bovine cytochrome P-45011β
  105. Photoaffinity labelling of the human mineralocorticoid receptor with steroids having a reactive group at position 3, 18 or 21
  106. Structure-activity relationships in 2-aminodiphenylsulfides against trypanothione reductase from Trypanosoma cruzi
  107. A General Approach to the Synthesis of Polyamine Linked-Monoindolylmaleimides, a New Series of Trypanothione Reductase Inhibitors.
  108. New spermine and spermidine derivatives as potent inhibitors of Trypanosoma cruzi Trypanothione Reductase
  109. Glutathione-dependent activities of Trypanosoma cruzi p52 makes it a new member of the thiol:disulphide oxidoreductase family
  110. New potent inhibitors of trypanothione reductase from Trypanosoma cruzi in the 2-aminodiphenylsulfide series
  111. New Steroidal Diazo Ketones as Potential Photoaffinity Labeling Reagents for the Mineralocorticoid Receptor:  Synthesis and Biological Activities
  112. The mineralocorticoid activity of progesterone derivatives depends on the nature of the C18 substituent.
  113. The mineralocorticoid activity of progesterone derivatives depends on the nature of the C18 substituent
  114. Synthesis of potential cytochrome P45011β-generated intermediates
  115. Purification of Microsomal Native Cytochrome b5 fromPotato Tubers (Solanum tuberosum L.)
  116. An improved synthesis of 18-norandrost-4-ene-3,17-dione
  117. High Sensitivity to Auxin is a Common Feature of Hairy Root
  118. Iridoid Glucosides and Phenylpropanoid Glycosides fromDeplanchea speciosa
  119. Epiallo-yohimbine derivatives isolated from in vitro hairy-root cultures of Catharanthus trichophyllus
  120. Production of indole alkaloids by in vitro root cultures from Catharanthus trichophyllus
  121. Iridoids ofRandia ruiziana
  122. Structure and Synthesis of Cucumopine, a New Crown Gall and Hairy-root Opine
  123. Cucumopine—a new T-DNA-encoded opine in hairy root and crown gall
  124. Iridoids of Guyanese Species of Stigmaphyllon