Frank Scheffler will be attending the 33rd Medicinal Chemistry in Eastern England meeting in Hatfield on Thursday 28th April 2022.
Known colloquially as the “Hatfield MedChem” meeting, this is a long-standing, one-day meeting which runs annually.
The scientific program comprises presentations showcasing medicinal chemistry case studies from tools to candidates, across a range of modalities, therapeutic areas and target classes, as well as covering more general topics from the forefront of drug discovery of relevance to medicinal chemist.
Programme
9:00 Registration/Coffee
MORNING SESSION Chair: Alison Jones (Charles River)
09:30 Welcome and Introduction
09:35 The discovery of novel GPR52 agonists: HTL0041178, a potential therapy for schizoaffective and related psychiatric disorders
Steve Watson (Heptares)
10:10 Discovery and development of first-in-class USP19 inhibitors for the treatment of metabolic and muscle-wasting disease
Shane Rountree (Almac)
10:45 Refreshments
11:10 Development and characterisation of 2-imino-hexahydropyrimidin-4-one derived Plasmepsin X inhibitors with in vivo anti-malarial activity
Teresa de Haro (UCB)
11:45 The Development of MNK Protacs
Martin Ambler (LifeArc)
12:10 Discovery and optimisation of allosteric inhibitors of Glutaminase 1 (GLS1)
Mark Charles (Cancer Research UK)
12:35 Lunch
AFTERNOON SESSION Chair: Simon Ward (Medicines Discovery Institute, Cardiff University)
13:30 Capps Green Zomaya Award Lecture
Jeremy Besnard (Exscientia)
14:05 Development of MAP4K4 Inhibitors for the Suppression of Cardiac Muscle Cell Death
Nick Martin (Domainex)
14:40 Accelerating decision making through parallel med chem
Neal Fazakerley (GSK)
15:05 Refreshments
15:30 Next generation estrogen receptor degraders (SERDs): A decade of discovery at AstraZeneca
Samantha Hughes (Astra Zeneca)
16:05 Discovery of novel LasB inhibitors as an inhaled antivirulence therapy for the treatment of Pseudomonas aeruginosa infections in patients with chronic respiratory disease
David Davies (Antabio)
16:30 Discovery and first disclosure of DDU209 a potent and selective inhibitor of Lysyl tRNA synthetase for Tuberculosis
Laura Cleghorn (Dundee Drug Discovery Unit, Univ Dundee)
16:55 Concluding Remarks
17:00 Meeting close