All Stories

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