Drug Discovery Chemistry

The discovery of candidate drug targets is exhausting and challenging, requiring the rapid development of techniques to identify the difference genomic profiling in disease and normal conditions, which will help in  understanding of the mechanism of diseases and the development of potential drugs can be processed for treatment of the disease. Medicinal chemistry has increasingly involved microarrays to identify both key target genes and gene networks that can regulate the effectiveness of drugs. As compared with all the other phases in drug discovery, this stage is complex by the fact that the identified drug target must mollify a variety of standards to permit development to the next step.  Example, the target should be selectively present in the pathogen, i.e. medicinal chemistry along with the  coding genes of drug design target that are present across different pathogens and have no human homolog connection and therefore they represent striking target candidates for new broad-spectrum drugs. These important topics will be covered in this current multi international gathering to get a proper insight from the renounced people belonging to this field.

  • Fragment-Based Drug Discovery
  • Macrocyclics & Constrained Peptides
  • Biophysical Approaches for Drug Discovery
  • Small Molecules for Cancer Immunotherapy
  • Inflammation Inhibitors
  • Protein-Protein Interactions
  • GPCR-Targeted Drug Design
  • Blood-Brain Penetrate Inhibitors
  • Kinase Inhibitor Chemistry

 




 


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