Cohort 4 (2022-2026) | MoSMed CDT

Natalie Roper

Institution: Newcastle University

Project Summary: Introducing a bulky ortho-substituent to sp²- rich amides or biaryls gives rise to two enantiomers, which can show drastically different pharmacokinetic and pharmacodynamic properties. Typically, a large tert-butyl group is required to prevent racemisation of these 3D compounds, however the high lipophilicity of this group limits its applications in drug discovery. This project focuses on replacing this group with more medicinally relevant locking groups.