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Novel N-heterocyclic carbene Gold-Selenium complexes: Green Synthesis and Anticancer Activity

Sector: Chemical (Industrial) • Location: Belgium

Source: EU Funding & Tenders Portal

Project
Ongoing

"This project aims to design new anticancer drugs by using N-heterocyclic carbenes (NHC), gold (Au), and selenium (Se), which have not been explored before. NHCs are chosen as key ligands in homogeneous catalysis with transition metals. Gold compounds, like auranofin, disrupt tumor growth by inhibiting key enzymes. Se triggers cancer cell death by inducing oxidative stress and blocking sulfur-bas

Status
Under Construction
Sector
Chemical (Industrial), Manufacturing (Industrial), Road, Government, Education
Location
Belgium
Updated
22 Jul 2026
Source
EU Funding & Tenders Portal

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The project “Novel N-heterocyclic carbene Gold-Selenium complexes: Green Synthesis and Anticancer Activity” is an infrastructure initiative in the Chemical (Industrial) sector, located in Belgium. Taiyo aggregates data on it from EU Funding & Tenders Portal.

Participants

Sponsoring Agency

Status

Original status

ongoing

Taiyo status

Under Construction

Taiyo last update

2026-07-22

Contact

Not available for this record.

Description

Description

"This project aims to design new anticancer drugs by using N-heterocyclic carbenes (NHC), gold (Au), and selenium (Se), which have not been explored before. NHCs are chosen as key ligands in homogeneous catalysis with transition metals. Gold compounds, like auranofin, disrupt tumor growth by inhibiting key enzymes. Se triggers cancer cell death by inducing oxidative stress and blocking sulfur-based cell components. Cancer poses a global threat, causing millions of deaths and huge economic losses, while available chemotherapy often leads to severe side effects and drug resistance. Therefore, there is a need for more effective and less toxic drugs. I synthesized and tested several drug candidates in in vitro cancer models, showing selective anticancer activity superior to cisplatin. The project uses a ""weak base route"" to synthesize these new compounds, following green chemistry principles to reduce the ecological impact of chemical synthesis. The proposed synthetic strategy uses non-toxic solvents and energy-saving protocols to promote sustainable drug development. Cell-free and cell-based assays will assess cytotoxicity, efficacy, and selectivity towards the TrxR1 enzyme, which is critical to cancer growth. Molecular docking will confirm the inhibition of the biological target, allowing structure-activity relationship (SAR) analysis to optimize drug structure. By refining the NHC ligand, Au-Se linker, and low core scaffold, the project aims to develop highly effective, targeted anticancer drugs. This research seeks to advance cancer treatment by creating targeted drugs that reduce side effects and improve patient outcomes. Additionally, it aligns with the EU's sustainability goals, promoting environmentally responsible drug development. The project also strengthens European cooperation in cancer research, both in academia and industry, and will inspire future chemists, with broader economic benefits through innovation in healthcare."

Location

Country

Belgium

Source

Source

EU Funding & Tenders Portal

URL

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Record type

Project

Sector

Chemical (Industrial), Manufacturing (Industrial), Road, Government, Education

Article published date

2026-01-01

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