Webinar
From Phenotypic Hit to an Orally Active Zika Antiviral
This webinar is designed for medicinal chemists, virologists, structural and molecular biologists, DMPK and pharmacology scientists, drug-discovery project leaders and R&D decision makers interested in antiviral research. It will be particularly relevant to teams seeking to translate phenotypic hits into differentiated leads by identifying their molecular targets, elucidating their mechanisms of action, and integrating structure-guided design with multidisciplinary lead optimization.
Attendees Will Gain Insights Into:
- How phenotypic screening identified IRBM-Z-1 as a starting point for Zika antiviral discovery
- How resistance selection, enzymology, and structural biology uncovered a novel allosteric site on the ZIKV NS2B-NS3 protease and elucidated its mechanism of inhibition
- How medicinal chemistry advanced IRBM-Z-1 to the orally active compound IRBM-Z-2
- How virology, medicinal chemistry, DMPK, and in vivo pharmacology were integrated to improve potency, selectivity, and pharmacokinetic properties and achieve efficacy in mouse models
How this allosteric inhibition strategy could open new opportunities for drug discovery against other clinically relevant flaviviruses