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1st MC4DD Workshop: 15-25 September 2025
TU Darmstadt Darmstadt Germany |
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We are bringing together world-leading experts to explore the frontiers of macrocycles in modern drug discovery!
Join us online 1st Thursday every month at 17:00 (Berlin time, unless otherwise noted) join us via Zoom Link: https://tu-darmstadt.zoom-x.de/j/64384397721?pwd=0bWgCcqVS4PDAQckDQVER9wzcAsZu4.1 Upcoming Lectures 06 November 2025: (Thursday) 17:00 Giulia Caron (Univeristy of Torino, IT): Property-Based Drug Design: Principles and Adapting Ro5 Strategies to Macrocycles 17:45 Sereina Riniker (ETH Zurich, CH): In Silico Exploration of Cyclic Peptides – Structure-Permeability Relationships 04 December 2025: (Thursday) 17:00 Adrian Whitty (Boston University, US): What does a 'druglike macrocycle' look like 17:45 Andrei Yudin (University of Toronto, CA): Strategic replacement of amino acid residues in macrocycles: Enabling iterative construction of novel scaffolds for drug discovery 05 Feburary 2026 17:00 Felix Hausch (Technical University Darmstadt, DE): Cyclic linkerology – the art of closing ends 17:45 Nele-Johanna Hempel-Højgaard (NovoNordisk, DK): Peptidic macrocycles – an upcoming modality 05 March 2026 17:00 Hiroaki Suga (University of Tokyo, JP): Pseudonatural macrocycles 17:45 Frauke Pohlki (AbbVie, DE): Macrocyclic MCL-1 Inhibitors 02 April 2026 13:00 Weibo Yang (Shanghai Institute of Materia Medica, Chinese Academy of Science, CN) 13:45 Ryuji Hayashi (Chugai, JP) Orally Bioavailable Cyclic Peptide Drug Discovery Platform Targeting an Intracellular Protein 28 May 2026 17:00 Pierre-Luc Boudreault (University of Sherbrooke, CA): Macrocycles as Next-Generation Non-Opioid Analgesics Targeting NTS2 17:45 tbd ------------------------------------------------------------------ Past Lectures 09 October 2025: (Thursday) 17:00 Scott Lokey (UC Santa Cruz, US): Investigating Structure-permeability relationships in cyclic peptide scaffolds using mass-encoded libraries 17:45 Jan Kihlberg (Uppsala University, SE): Macrocycles in Drug Discovery - Reaching intracellular difficult-to-drug targets
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