All Stories

  1. Cell permeable affinity- and activity-based probes
  2. Rational Targeting of Active-Site Tyrosine Residues Using Sulfonyl Fluoride Probes
  3. Sulfonyl fluorides as privileged warheads in chemical biology
  4. TAK1 selective inhibition: state of the art and future opportunities
  5. Chemical biology & drug discovery
  6. Biotherapeutics: Recent Developments using Chemical and Molecular Biology. Edited by Lyn H. Jones, Andrew J. McKnight
  7. Rare diseases
  8. Synthetic Phosphorylation of p38α Recapitulates Protein Kinase Activity
  9. Target validation using in-cell small molecule clickable imaging probes
  10. Understanding and applying tyrosine biochemical diversity
  11. Aryloxymaleimides for cysteine modification, disulfide bridging and the dual functionalization of disulfide bonds
  12. TAK1 Inhibition in the DFG-Out Conformation
  13. Selection of a Novel Anti-Nicotine Vaccine: Influence of Antigen Design on Antibody Function in Mice
  14. A mild synthesis of N-functionalised bromomaleimides, thiomaleimides and bromopyridazinediones
  15. Target validation using chemical probes
  16. Developing Irreversible Inhibitors of the Protein Kinase Cysteinome
  17. Biotherapeutics
  18. Chemical motifs that redox cycle and their associated toxicity
  19. Chemistry and Biology of Biomolecule Nitration
  20. ChemInform Abstract: Molecular Scaffolds Using Multiple Orthogonal Conjugations: Applications in Chemical Biology and Drug Discovery
  21. Mehrfache orthogonale Konjugationen mit Molekülgerüsten: Anwendung in der chemischen Biologie und Wirkstoff-Forschung
  22. Molecular Scaffolds Using Multiple Orthogonal Conjugations: Applications in Chemical Biology and Drug Discovery
  23. Welcome to Pharmaceutical Patent Analyst
  24. Quantitative affinity-based chemical proteomics of TrkA inhibitors
  25. Click-enabled heterotrifunctional template for sequential bioconjugations
  26. Uptake, Efficacy, and Systemic Distribution of Naked, Inhaled Short Interfering RNA (siRNA) and Locked Nucleic Acid (LNA) Antisense
  27. Efficient Conversion of a Nonselective Norepinephrin Reuptake Inhibitor into a Dual Muscarinic Antagonist−β 2 -Agonist for the Treatment of Chronic Obstructive Pulmonary Disease
  28. Inhalation by design
  29. Dual-pharmacology muscarinic antagonist and β2agonist molecules for the treatment of chronic obstructive pulmonary disease
  30. ChemInform Abstract: Squaramides: Physical Properties, Synthesis and Applications
  31. Inhalation by design: Dual pharmacology β-2 agonists/M3 antagonists for the treatment of COPD
  32. ChemInform Abstract: Aromatic Chloride to Nitrile Transformation: Medicinal and Synthetic Chemistry
  33. Comparison of the Non-Nucleoside Reverse Transcriptase Inhibitor Lersivirine with its Pyrazole and Imidazole Isomers
  34. Squaramides: physical properties, synthesis and applications
  35. Optimized glucuronidation of dual pharmacology β-2 agonists/M3 antagonists for the treatment of COPD
  36. In-cell click labelling of small molecules to determine subcellular localisation
  37. Aromatic chloride to nitrile transformation: medicinal and synthetic chemistry
  38. Chapter 6. Chemologics
  39. Thermodynamic Optimisation in Drug Discovery: A Case Study using Carbonic Anhydrase Inhibitors
  40. Pyrazole NNRTIs 3: Optimisation of physicochemical properties
  41. ChemInform Abstract: Relaying Stereochemistry Through Aromatic Ureas: 1,9 and 1,15 Remote Stereocontrol.
  42. Physicochemical drug properties associated within vivotoxicological outcomes: a review
  43. Novel Indazole Non-Nucleoside Reverse Transcriptase Inhibitors Using Molecular Hybridization Based on Crystallographic Overlays †
  44. Relaying stereochemistry through aromatic ureas: 1,9 and 1,15 remote stereocontrol
  45. Optimization of 5-Aryloxyimidazole Non-Nucleoside Reverse Transcriptase Inhibitors
  46. Helix Persistence and Breakdown in Oligoureas of Metaphenylenediamine: Apparent Diastereotopicity as a Spectroscopic Marker of Helix Length in Solution
  47. ChemInform Abstract: Synthetic Chemistry-Led Creation of a Difluorinated Biaryl Ether Non-Nucleoside Reverse Transcriptase Inhibitor.
  48. Conformation and stereodynamics of 2,2′-disubstituted N,N′-diaryl ureas
  49. Design and synthesis of a fluorescent muscarinic antagonist
  50. Synthetic chemistry-led creation of a difluorinated biaryl ether non-nucleoside reverse transcriptase inhibitor
  51. Novel selective inhibitors of neutral endopeptidase for the treatment of female sexual arousal disorder
  52. A Concise Synthesis of Trifluoromethyl-Substituted 4-Aryloxy Pyrazoles
  53. A Concise and Selective Synthesis of Novel 5-Aryloxyimidazole NNRTIs
  54. Oxaziridine-Mediated Amination of Primary Amines: Scope and Application to a One-Pot Pyrazole Synthesis.
  55. Oxaziridine-Mediated Amination of Primary Amines: Scope and Application to a One-Pot Pyrazole Synthesis
  56. Active Immunization with a Glycolipid Transition State Analogue Protects against Endotoxic Shock
  57. Antibody Catalysis of the Oxidation of Water
  58. The Therapeutic Potential for Catalytic Antibodies From a Concept to a Promise
  59. Conversion of Enediynes into Quinones by Antibody Catalysis and in Aqueous Buffers:  Implications for an Alternative Enediyne Therapeutic Mechanism
  60. ChemInform Abstract: Total Synthesis of (+)-Zaragozic Acid C.
  61. Total Synthesis of (+)-Zaragozic Acid C
  62. Antibodies have the intrinsic capacity to destroy antigens
  63. Cleavage of the cyclohexyl-subunit of rapamycin results in loss of immunosuppressive activity
  64. Total synthesis of (+)-zaragozic acid C