Related Experiment Video
Updated: Jun 13, 2025

Kinase Inhibitor Screening In Self-assembled Human Protein Microarrays
Published on: October 23, 2019
An updated patent review of rearranged during transfection (RET) kinase inhibitors (2022-present)
Daniel Armstrong1, Maha Hanafi1,2, Brendan Frett1
1Department of Pharmaceutical Sciences, College of Pharmacy, University of Arkansas for Medical Sciences, Little Rock, AR, USA.
Introduction:
Rearranged during transfection (RET) is a receptor tyrosine kinase essential for cell signaling processes such as proliferation, differentiation, and migration. RET alterations, including point mutations and gene fusions, contribute to oncogenesis. Recent advances in precision oncology have led to the development of selective RET inhibitors with improved safety and efficacy profiles.
Areas Covered:
This review discusses recent innovations in RET inhibitor development, with a focus on small-molecule patents published from 2022 to 2024. A comprehensive literature search was conducted using SciFinder and PatentScope with the keywords 'RET' and 'RET inhibitor.' The review summarizes the structural classes, target profiles, and potential advantages of newly patented compounds, particularly those designed to overcome known resistance mechanisms.
Expert Opinion:
While selective RET inhibitors such as selpercatinib have shown clinical success and expanded indications, their use is limited by adverse events and emerging resistance mechanisms. Next-generation RET inhibitors that address these limitations represent a critical frontier in drug development.
Insights
Recent patents reveal novel small-molecule Rearranged during transfection (RET) inhibitors designed to overcome resistance and improve safety. These next-generation drugs offer a critical advancement in precision oncology for RET-driven cancers.
Area of Science:
- Oncology
- Pharmacology
- Molecular Biology
Background:
- Rearranged during transfection (RET) is a receptor tyrosine kinase vital for cell signaling.
- Alterations in RET, including mutations and fusions, are implicated in cancer development.
- Selective RET inhibitors have emerged as a precision oncology strategy.
Purpose of the Study:
- To review recent innovations in RET inhibitor development.
- To focus on small-molecule patents from 2022-2024.
- To summarize structural classes, target profiles, and advantages of new compounds, especially in overcoming resistance.
Main Methods:
- Comprehensive literature search using SciFinder and PatentScope.
- Keywords: 'RET', 'RET inhibitor'.
- Analysis of patented small-molecule RET inhibitors.
Main Results:
- Identification of novel structural classes of RET inhibitors.
- Characterization of target profiles for new compounds.
- Highlighting compounds designed to address known resistance mechanisms.
Conclusions:
- Next-generation RET inhibitors are crucial for advancing cancer treatment.
- New patented compounds show promise in overcoming limitations of current therapies.
- Continued development of selective RET inhibitors is a key frontier in precision oncology.
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