New compounds can activate prodrugs at predetermined locations in the body

New compounds can activate prodrugs at predetermined locations in the body
Accelerated activation of prodrugs using improved activators developed in Milan Vrabel Group. Their discovery paves the way for the design of innovative activation strategies to achieve more effective treatments for diseases such as cancer, with fewer side effects. Credit: IOCB Prague

Researchers from IOCB Prague have succeeded in preparing compounds capable of activating prodrugs at predetermined locations in the body, enhancing their effectiveness and expediting their action. This will make it possible, for example, to more precisely target malignant tumors, which might greatly advance the potential of anti-cancer therapies.

Compounds referred to as new-generation prodrug activators have been developed in the laboratory of Dr. Milan Vrábel, and two research articles on the matter have been published in the journal Angewandte Chemie International Edition.

One objective of modern medicine is to utilize substances known as prodrugs, which are medicinal compounds that can be activated by being metabolically converted into drugs in specific parts of the body, for example near or inside cancerous tumors. It is not an easy process, because prodrugs tend to initiate their function in all sorts of places in the body.

This is where compounds known as activators come into play. With their application, a specific chemical reaction is used to “unpack” the prodrug in the right location. However, the current generation of activators is slow and ineffective. Molecules of an active substance are usually released only after several hours, and the body can typically utilize only about 60% of the administered dose.

Therefore, a research team at IOCB Prague, in collaboration with colleagues from the Technical University of Vienna, is working toward markedly enhancing the properties of prodrug activators.

“Our latest generation of activators allows for the complete release of the drug in a very short time of about half an hour,” says Vrábel. “We have proved the greater release speed and pharmacological efficacy in several exemplary in vitro cellular experiments.”

The use of prodrug activators is being explored not only by researchers in basic science, but also by the pharmaceutical industry, and the first phase of clinical trials have already been completed. Although these are early, imperfect versions of prodrug activators, there is already evidence that this concept works in the human body.

If, thanks to the research carried out at IOCB Prague, the properties of these molecules are successfully improved, more effective treatments for various diseases, including cancer, will be within reach.

More information:
Martin Wilkovitsch et al, Transforming Aryl‐Tetrazines into Bioorthogonal Scissors for Systematic Cleavage of trans‐Cyclooctenes, Angewandte Chemie International Edition (2024). DOI: 10.1002/anie.202411707

Michal Rahm et al, Sulfonated Hydroxyaryl‐Tetrazines with Increased pKa for Accelerated Bioorthogonal Click‐to‐Release Reactions in Cells, Angewandte Chemie International Edition (2024). DOI: 10.1002/anie.202411713

Provided by
Institute of Organic Chemistry and Biochemistry of the CAS

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New compounds can activate prodrugs at predetermined locations in the body (2024, October 15)
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