All Stories

  1. Toward Small-Molecule Inhibition of Protein–Protein Interactions: General Aspects and Recent Progress in Targeting Costimulatory and Coinhibitory (Immune Checkpoint) Interactions
  2. Fully Automated Islet Cell Counter (ICC) for the Assessment of Islet Mass, Purity, and Size Distribution by Digital Image Analysis
  3. TNF Superfamily Protein-Protein Interactions: Feasibility of Small- Molecule Modulation
  4. Small‐molecule modulators of the OX40–OX40 ligand co‐stimulatory protein–protein interaction
  5. Effects of representative glucocorticoids on TNFα- and CD40L-induced NF-κB activation in sensor cells
  6. Bilinear Model for the Size‐Dependency of the CYP3A4 Inhibitory Activity of Structurally Diverse Compounds
  7. The promiscuous protein binding ability of erythrosine B studied by metachromasy (metachromasia)
  8. Retrometabolic Drug Design and Targeting
  9. Retrometabolism‐Based Drug Design and Targeting
  10. Glucocorticoid receptor binding: A biphasic dependence on molecular size as revealed by the bilinear LinBiExp model
  11. Retrometabolic drug design: Principles and recent developments
  12. Computer-aided retrometabolic drug design: soft drugs
  13. A general bilinear model to describe growth or decline time profiles
  14. Targeting of Neuropharmaceuticals by Chemical Delivery Systems
  15. General Linearized Biexponential Model for QSAR Data Showing Bilinear-Type Distribution
  16. Designing Safer (Soft) Drugs by Avoiding the Formation of Toxic and Oxidative Metabolites
  17. Retrometabolism‐Based Drug Design and Targeting
  18. Brain-Targeted Drug Delivery
  19. Barriers to remember: brain-targeting chemical delivery systems and Alzheimer's disease
  20. Structure-Metabolism Relationships Steric Effects and the Enzymatic Hydrolysis of Carboxylic Esters
  21. ChemInform Abstract: Soft Drug Design: General Principles and Recent Applications
  22. Soft drug design: General principles and recent applications
  23. Soft drug design: General principles and recent applications
  24. Drug targeting via retrometabolic approaches
  25. Designing Safer (Soft) Drugs by Avoiding the Formation of Toxic and Oxidative Metabolites