
Benhamou Research Group
Chemical Biology & Drug Design
About the lab
Our research laboratory is dedicated to the emerging field of RNA-targeted therapeutics, integrating chemical biology, medicinal chemistry, and molecular/cellular biology. We leverage organic chemistry to develop molecules that selectively bind to RNA complexes, aiming to modulate RNA function in disease-relevant models. These compounds serve as chemical probes to explore RNA biology or as therapeutic candidates to correct aberrant RNA processes. Furthermore, we are actively engaged in targeted degradation technologies, designing molecular glues, PROTAC-like degraders, and RNA-targeting chimeras that recruit endogenous cellular machinery to degrade pathogenic RNA complexes. This approach enables the selective elimination of disease-associated RNA complexes, offering a novel therapeutic strategy for conditions driven by RNA dysregulation. Our research spans a broad range of diseases, including cancer, genetic disorders, metabolic syndromes, brain diseases, and infectious diseases, with the ultimate goal of pioneering innovative RNA-targeted therapeutic solutions.

News & Events
26.10.25: We welcome to our lab two new Master students Esther and Leen!
15.10.25: Excited to share our new publication in Advanced Science! Congrats Elias! "RNA G-Quadruplex RIBOTAC-Mediated Targeted Degradation of lncRNA TERRA".
04.09.2025: Delighted to share our newest publication in ACS Pharmacology & Translational Science! Congrats Aseel! Development of PROTAC-Based Strategies for Cannabinoid Receptor Type 1 (CB1R) Degradation in Cancer
25.08.25: Thrilled to share that our work on druglike degraders of HuR has been selected for the JACS Au cover!
04.08.25: Congratulations to Elias for receiving the best poster award at the MCS-ICS 2025 annual conference!
25.07.25: Congratulations to Aseel Kashkush for receiving the Best Master's Student Prize from the Faculty of Medicine at the Hebrew University!
16.07.25: New published Article In JACS Au! Congrats Liann! "Druglike Molecular Degraders of the Oncogenic RNA-Binding Protein HuR".






