All Stories

  1. Synthetic Kavalactone Analogues with Increased Potency and Selective Anthelmintic Activity against Larvae of Haemonchus contortus In Vitro
  2. Screening the Medicines for Malaria Venture Pathogen Box for invasion and egress inhibitors of the blood stage of Plasmodium falciparum reveals several inhibitory compounds
  3. Screening the Medicines for Malaria Venture Pathogen Box for invasion and egress inhibitors of the blood stage of Plasmodium falciparum reveals several inhibitory compounds
  4. The Development Process for Discovery and Clinical Advancement of Modern Antimalarials
  5. An appraisal of natural products active against parasitic nematodes of animals
  6. Identification of 5-Substituted 2-Acylaminothiazoles That Activate Tat-Mediated Transcription in HIV-1 Latency Models
  7. Evaluation of 4-Amino 2-Anilinoquinazolines against Plasmodium and Other Apicomplexan Parasites In Vitro and in a P. falciparum Humanized NOD-scid IL2Rγnull Mouse Model of Malaria
  8. Enhanced antimalarial activity of plasmepsin V inhibitors by modification of the P 2 position of PEXEL peptidomimetics
  9. Conversion of Bim-BH3 from Activator to Inhibitor of Bak through Structure-Based Design
  10. Screening the Medicines for Malaria Venture Pathogen Box across Multiple Pathogens Reclassifies Starting Points for Open-Source Drug Discovery
  11. Mefloquine targets the Plasmodium falciparum 80S ribosome to inhibit protein synthesis
  12. Optimization of 2-Anilino 4-Amino Substituted Quinazolines into Potent Antimalarial Agents with Oral in Vivo Activity
  13. Analysis of Ca2 + mediated signaling regulating Toxoplasma infectivity reveals complex relationships between key molecules
  14. Exploration of the P 3 region of PEXEL peptidomimetics leads to a potent inhibitor of the Plasmodium protease, plasmepsin V
  15. Synthesis of amino heterocycle aspartyl protease inhibitors
  16. Reversible and formaldehyde-mediated covalent binding of a bis-amino mitoxantrone analogue to DNA
  17. Isolation and structural analysis of the covalent adduct formed between a bis-amino mitoxantrone analogue and DNA: a pathway to major–minor groove cross-linked adducts
  18. An aspartyl protease defines a novel pathway for export of Toxoplasma proteins into the host cell
  19. HIV-1 and Human PEG10 Frameshift Elements Are Functionally Distinct and Distinguished by Novel Small Molecule Modulators
  20. Mitoxantrone, More than Just Another Topoisomerase II Poison
  21. Structural basis for plasmepsin V inhibition that blocks export of malaria proteins to human erythrocytes
  22. Macrolides rapidly inhibit red blood cell invasion by the human malaria parasite, Plasmodium falciparum
  23. The effect of N-methylation on transition state mimetic inhibitors of the Plasmodium protease, plasmepsin V
  24. Macrocyclic N-Methylated Cyclic Peptides and Depsipeptides
  25. Discovery of a Potent and Selective BCL-X L Inhibitor with in Vivo Activity
  26. Transition State Mimetics of the Plasmodium Export Element Are Potent Inhibitors of Plasmepsin V from P. falciparum and P. vivax
  27. Inhibition of Plasmepsin V Activity Demonstrates Its Essential Role in Protein Export, PfEMP1 Display, and Survival of Malaria Parasites
  28. Structure-Guided Rescaffolding of Selective Antagonists of BCL-X L
  29. Stereoselective Synthesis and Application of β-Amino Ketones
  30. Discovery of Potent and Selective Benzothiazole Hydrazone Inhibitors of Bcl-X L
  31. Diastereoselective synthesis of cyclic β2,3-amino acids utilizing 4-substituted-1,3-oxazinan-6-ones
  32. Structure-guided design of a selective BCL-XL inhibitor
  33. Synthesis of N-Cbz-Substituted β3-Amino Ketones Utilizing 4-Substituted 1,3-Oxazinan-6-ones
  34. A Mild Multistep Conversion of N-Protected α-Amino Acids into N-Protected β3-Amino Acids Utilizing the Nef Reaction
  35. Role of Plasmepsin V in Export of Diverse Protein Families from the Plasmodium falciparum Exportome
  36. Corrigendum to “Diastereoselective synthesis of highly functionalized β2,2,3-substituted amino acids from 4-substituted-1,3-oxazinan-6-ones” [Tetrahedron 68 (2012) 4745–4756]
  37. Diastereoselective synthesis of highly functionalized β2,2,3-substituted amino acids from 4-substituted-1,3-oxazinan-6-ones
  38. Corrigendum to “Identification of 5,6-substituted 4-aminothieno[2,3-d]pyrimidines as LIMK1 inhibitors” [Bioorg. Med. Chem. Lett. 21 (2011) 5992–5994]
  39. M2, a novel anthracenedione, elicits a potent DNA damage response that can be subverted through checkpoint kinase inhibition to generate mitotic catastrophe
  40. Identification of 5,6-substituted 4-aminothieno[2,3-d]pyrimidines as LIMK1 inhibitors
  41. Quinazoline Sulfonamides as Dual Binders of the Proteins B-Cell Lymphoma 2 and B-Cell Lymphoma Extra Long with Potent Proapoptotic Cell-Based Activity
  42. Identification of 3-aminothieno[2,3-b]pyridine-2-carboxamides and 4-aminobenzothieno[3,2-d]pyrimidines as LIMK1 inhibitors
  43. Development of substituted 7-phenyl-4-aminobenzothieno[3,2-d] pyrimidines as potent LIMK1 inhibitors
  44. New Anthracenedione Derivatives with Improved Biological Activity by Virtue of Stable Drug−DNA Adduct Formation
  45. De Novo Synthesis of a Potent LIMK1 Inhibitor
  46. Recent Advances in Stereoselective Synthesis and Application of β-Amino Acids
  47. Conformational Changes in Bcl-2 Pro-survival Proteins Determine Their Capacity to Bind Ligands
  48. Studies of 2-Substituted 1,3-Oxazolidin-5-ones and 1,3-Oxazinan-6-ones as Precursors for the Synthesis ofN-Alkyl-β-Amino Acids
  49. Exploitation of the Arndt-Eistert Homologation of N-Methyl-�-Amino Acids for Concomitant Ester and N-Methyl Peptide Formation
  50. Diastereoselective Synthesis of α-Methyl and α-Hydroxy-β-Amino Acids via 4-Substituted-1,3-Oxazinan-6-ones
  51. Effective Methods for the Synthesis ofN-Methylβ-Amino Acids from All Twenty Commonα-Amino Acids Using 1,3-Oxazolidin-5-ones and 1,3-Oxazinan-6-ones
  52. Synthesis of New β-Amino Acids via 5-Oxazolidinones and the Arndt–Eistert Procedure