Understanding Pemigatinib: A Potent FGFR Inhibitor for Cholangiocarcinoma and Beyond
Exploring the science behind a targeted therapy that's changing the landscape of cancer treatment.
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FGFR Inhibitor
This advanced pharmaceutical compound is recognized for its potent and selective inhibition of Fibroblast Growth Factor Receptors (FGFRs), particularly FGFR1-3. Its efficacy against specific gatekeeper mutations, such as FGFR2 V564I, makes it a critical tool in the fight against certain cancers, offering a targeted approach to treatment.
- Discover the precise FGFR inhibitor mechanism of action that targets FGFR2 fusions in cholangiocarcinoma treatment.
- Learn about the structural basis for high potency, crucial for understanding pemigatinib's therapeutic effect.
- Analyze the pemigatinib gatekeeper mutation efficacy, especially its activity against FGFR2 V564I.
- Explore how this drug provides insights for next-generation FGFR inhibitor design and overcoming drug resistance.
Key Advantages
Targeted Efficacy
The drug offers potent and selective inhibition of FGFR1-3, a critical advantage in targeting specific cancer pathways, including those driven by FGFR2 fusions.
Resistance Management Insights
The research elucidates pemigatinib's effectiveness against certain gatekeeper mutations, providing vital clues for developing strategies to combat drug resistance in cancer therapy.
Structural Understanding
Detailed structural analysis reveals the intricate binding mechanism between the inhibitor and FGFR1, aiding in the design of more effective and selective future therapeutics.
Key Applications
Oncology
This inhibitor plays a crucial role in oncology, specifically in the treatment of cholangiocarcinoma driven by FGFR2 alterations.
Cancer Treatment Research
Its mechanism and efficacy are extensively studied to advance precision medicine and improve outcomes in various FGFR-driven malignancies.
Drug Discovery
The compound serves as a benchmark and provides valuable insights for the discovery and development of novel kinase inhibitors targeting cancer.
Pharmaceutical Development
As a pharmaceutical intermediate or API, it is crucial for the synthesis of advanced therapeutics aimed at specific molecular targets in cancer.