All Stories

  1. Design, Synthesis and Antiproliferative Evaluation of Glucose 6ʺ-OH Modified Open-Chain Analogues of Ipomoeassin F
  2. A common mechanism of Sec61 translocon inhibition by small molecules
  3. A common mechanism of Sec61 translocon inhibition by small molecules
  4. Synthesis, Biological Evaluation and Docking Studies of Ring-Opened Analogues of Ipomoeassin F
  5. Co-translational biogenesis of lipid droplet integral membrane proteins
  6. Co-translational biogenesis of lipid droplet integral membrane proteins
  7. An alternative pathway for membrane protein biogenesis at the endoplasmic reticulum
  8. Ipomoeassin-F disrupts multiple aspects of secretory protein biogenesis
  9. A potentially new broad-spectrum antiviral: a SARS-CoV-2 in vitro study
  10. Ring Expansion Leads to a More Potent Analogue of Ipomoeassin F
  11. Ipomoeassin-F inhibits the in vitro biogenesis of the SARS-CoV-2 spike protein and its host cell membrane receptor
  12. Posttranslational insertion of small membrane proteins by the bacterial signal recognition particle
  13. Design and Synthesis of Tetrazole- and Pyridine-Containing Itraconazole Analogs as Potent Angiogenesis Inhibitors
  14. Ipomoeassin F Binds Sec61α to Inhibit Protein Translocation
  15. Ipomoeassin F Binds Sec61α to Inhibit Protein Translocation
  16. Canvass: A Crowd-Sourced, Natural-Product Screening Library for Exploring Biological Space
  17. Novel Tetrazole-Containing Analogues of Itraconazole as Potent Antiangiogenic Agents with Reduced Cytochrome P450 3A4 Inhibition
  18. Structure-activity relationship study of itraconazole, a broad-range inhibitor of picornavirus replication that targets oxysterol-binding protein (OSBP)
  19. New insights into structure–activity relationship of ipomoeassin F from its bioisosteric 5-oxa/aza analogues
  20. Design, synthesis and biological evaluation of fucose-truncated monosaccharide analogues of ipomoeassin F
  21. Synergistic Contribution of Tiglate and Cinnamate to Cytotoxicity of Ipomoeassin F
  22. Simultaneous Targeting of NPC1 and VDAC1 by Itraconazole Leads to Synergistic Inhibition of mTOR Signaling and Angiogenesis
  23. Divergence of Antiangiogenic Activity and Hepatotoxicity of Different Stereoisomers of Itraconazole
  24. Revealing the Pharmacophore of Ipomoeassin F through Molecular Editing
  25. Antifungal drug itraconazole targets VDAC1 to modulate the AMPK/mTOR signaling axis in endothelial cells
  26. Total Synthesis and Biological Evaluation of Ipomoeassin F and Its Unnatural 11R-Epimer
  27. Stereospecific Metabolism of Itraconazole by CYP3A4: Dioxolane Ring Scission of Azole Antifungals
  28. Itraconazole Side Chain Analogues: Structure–Activity Relationship Studies for Inhibition of Endothelial Cell Proliferation, Vascular Endothelial Growth Factor Receptor 2 (VEGFR2) Glycosylation, and Hedgehog Signaling
  29. Reprint of “Effect of carbohydrate amino group modifications on the cytotoxicity of glycosylated 2-phenyl-benzo[b]thiophenes and 2-phenyl-benzo[b]furans” [Bioorg. Med. Chem. Lett. 21 (2011) 2591–2596]
  30. Structure–activity relationships in glycosylated 2-phenyl-indoles, 2-phenyl-benzo[b]thiophenes and 2-phenyl-benzo[b]furans as DNA binding and potential antitumor agents
  31. Cytotoxicity and topoisomerase I/II inhibition of glycosylated 2-phenyl-indoles, 2-phenyl-benzo[b]thiophenes and 2-phenyl-benzo[b]furans
  32. Impact of Absolute Stereochemistry on the Antiangiogenic and Antifungal Activities of Itraconazole
  33. Determination of the absolute configurations of synthetic daunorubicin analogues using vibrational circular dichroism spectroscopy and density functional theory
  34. Synthesis and antibacterial activity of aminosugar-functionalized intercalating agents
  35. Synthesis and DNA-binding affinity studies of glycosylated intercalators designed as functional mimics of the anthracycline antibiotics
  36. Synthesis of Daunorubicin Analogues Containing Truncated Aromatic Cores and Unnatural Monosaccharide Residues
  37. Chemical and chemoenzymatic synthesis of a trisaccharide fragment of Tsukamurella paurometabola lipoarabinomannan
  38. A Divergent Synthesis of Triyne Natural Products and Glycosylated Analogues Using a Carbenoid Rearrangement