Provides the concepts and tools for developing drug-like small molecules that selectively target RNA rather than proteins, including the first successful examples from the development pipeline of big pharma.
Provides the concepts and tools for developing drug-like small molecules that selectively target RNA rather than proteins, including the first successful examples from the development pipeline of big pharma.
John Schneekloth received his undergraduate degree from Dartmouth College in 2001 where he worked with Prof. Gordon Gribble. He then moved to Yale University and obtained a Ph.D. from the chemistry department with Prof. Craig Crews in 2006. As a graduate student he studied natural product total synthesis and developed the first cell-permeable PROTAC molecules. He then pursued an NIH postdoctoral fellowship with Prof. Erik Sorensen at Princeton University where he worked on the development of a new multicomponent reaction and the application of this reaction to the synthesis of analgesic natural products. He returned to Yale in 2009 where he worked as a medicinal chemist at the Yale Small Molecule Discovery Center. In 2011, Dr. Schneekloth joined NCI where his research involves using synthetic chemistry and high throughput chemical biology approaches to develop chemical probes of RNA, with a particular emphasis on targeting RNA with druglike small molecules. Martin Pettersson is a medicinal chemistry / drug discovery leader with 18+ years of industrial experience. He received his undergraduate degree from Indiana University in 1998, working with David R. Williams. After four years working for Pfizer, he then joined the University of Texas at Austin for a Ph.D. in Organic Chemistry with Stephen F. Martin. He continued to work for Pfizer, where he delivered multiple compounds into clinical development. He co-led Pfizer's COVID-19 oral protease inhibitor program from project inception until August 2020, during which time the clinical candidate PF-07321332 (Paxlovid) was designed and synthesized. In 2020, he became senior director Neuroscience/Pain at Grünenthal Group, where he is also a member of the Research Board. His publication record includes more than 70 publications, patents/patent applications, and presentations.
Inhaltsangabe
1. Introduction 2. RNA Structure Probing, Dynamics, and Folding 3. High Resolution Structures of RNA 4. Screening and Lead Generation Techniques for RNA Binders 5. Chemical Matter that Binds RNA 6. MicroRNAs as Targets for Small Molecule Binders 7. Pre-mRNA Splicing Modulation 8. Prospects for Riboswitches in Drug Development 9. Small Molecules That Degrade RNA 10. Approaches to the Identification of Molecules Altering Programmed Ribosomal Frameshifting in Viruses 11. RNA-Protein Interactions: A New Approach for Drugging RNA Biology 12. Drugging the Epitranscriptome 13. Outlook. A Perspective on RNA: The Next Frontier for Small Molecule Therapeutics
1. Introduction 2. RNA Structure Probing, Dynamics, and Folding 3. High Resolution Structures of RNA 4. Screening and Lead Generation Techniques for RNA Binders 5. Chemical Matter that Binds RNA 6. MicroRNAs as Targets for Small Molecule Binders 7. Pre-mRNA Splicing Modulation 8. Prospects for Riboswitches in Drug Development 9. Small Molecules That Degrade RNA 10. Approaches to the Identification of Molecules Altering Programmed Ribosomal Frameshifting in Viruses 11. RNA-Protein Interactions: A New Approach for Drugging RNA Biology 12. Drugging the Epitranscriptome 13. Outlook. A Perspective on RNA: The Next Frontier for Small Molecule Therapeutics
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