Integrated fragment-based approach reveals enzymatic inhibitors with potential therapeutic application

Supported by:

25 October 2018

ABOUT THIS WEBINAR:

• Overview of IDO1 structure and functions
• Rise and fall of current IDO1 inhibitors in immune-oncology
•  The quest for next generation ligands of IDO1.
• Our integrated fragment-based approaches: focus on MST
• Discovery of chemical modulators of IDO1 non-catalytic signalling function

Indoleamine 2,3 dioxygenase 1 (IDO1) is an heme-containing enzyme that catalyses the conversion of L-Tryptophan (Trp) into a series of bioactive metabolites along the kynurenine pathway, eventually leading to immunoregulatory effects. These effects include induction of regulatory T-cell differentiation and activation, suppression of T-cell immune responses and inhibition of dendritic cell function.

On this basis, IDO1 is widely recognised as a valuable drug target for the development of immunotherapeutic small molecules in oncology. Although numerous chemical classes of potent IDO1 inhibitors that have been discovered, few compounds have progressed in clinical trials, while the most advanced drug candidate (Epacadostat) has unfortunately failed in phase III clinical trials in metastatic melanoma patients.

These disappointing results highlight the complexity of targeting IDO1 for drug discovery, and perhaps suggest a still elusive knowledge on its biological functions. Accordingly, next generation ligands are sought with the aim of investigating hidden and relevant aspects of IDO1 biology.

In this webinar, speakers presented results of integrated fragment-based approaches that have led to the discovery of the first ligands of IDO1 that are able to modulate non-catalytic signalling functions of the enzyme. They focused on MicroScale Thermophoresis (MST) as the cornerstone methodology of their discovery pipeline and concluded with an outlook on the impact of fragment-based approaches in the drug discovery of the post-genomic era.