
- CB1 Allosteric Enhancers
- CB1 Allosteric Inhibitors
- GPR55 Antagonists
- A Novel Target for Diastolic Heart Failure
- Novel Fungal Diagnostics and Therapeutics
- CB1 Receptor PET Ligands
- Rheumatoid Arthritis
- Antifungal Agents: chitin synthase inhibitors
- A Novel Treatment for Hypertension
- PET Tracers for Alzheimer's Disease
- Insulin Gene Therapy
- HIV Entry Inhibitors
- A Novel Target for Prostate Cancer
- A Novel Anthelmintic Target
- Neuroprotective Agents
- Hypothalamic Receptors for Metabolic Health
- SBF: Delivery of drugs across the BBB using shark VNAR biotools
- 18F-FDR as a New Powerful Radiolabelling Agent for PET
- PET Tracers for Hypoxia
- Angiogenesis Tracers
- Development of PET Tracers for Membrane Transporters
- A Novel Retinoid Pathway
Kosterlitz Projects
The Kosterlitz oversees a number of current projects which focus on target validation and drug discovery; the team works alongside Research & Innovation and the lead biologist for each project. These projects have generally started with biological innovation, e.g. relating to the discovery of a new receptor or pathway and involvement in a disease state. The Kosterlitz team are then ideally placed to add value to the discovery by: identification of relevant funding streams and assistance in preparation of grant applications, access as required to pharmacology, synthetic organic and medicinal chemistry for mechanism of action studies and generation of selective ligands for proof of principle and target validation.

Further development of the project may involve access to SULSA compound libraries and high-throughput screening, followed by an in-house or outsourced drug discovery campaign. The team can provide advice and contacts for conducting outsourced preclinical studies; can assist with the writing and filing of patent applications and,in concert with R&I, assist with finding suitable partners for a successful commercial conclusion to the project (where appropriate).
Furthermore, projects which are part of the Kosterlitz, have the added advantage of synergy with other projects, which may facilitate the sharing of data (e.g. common signalling pathways), resources (e.g. biological models and bioactive compounds) and personnel (e.g. chemistry and technical support may be split between projects), and joint grant applications.
Contacts:
Dr Iain Greig (i.greig@abdn.ac.uk) or Dr Ann Lewendon (a.lewendon@abdn.ac.uk)
University of Aberdeen
King's College
Aberdeen
AB24 3FX
