Structure-Based Design and Optimization of Novel, Potent and Selective Covalent FGFR2/3 Inhibitors with a Tricyclic Core
Abstract
demonstrated favorable oral bioavailability (56%) in rats and achieved significant tumor growth inhibition in an SNU-16 gastric cancer xenograft model.
Fields of Study & Subjects
Fibroblast Growth Factor Research
Fluorine in Organic Chemistry
Multicomponent Synthesis of Heterocycles
Publication details
- Journal / source
- Journal of Medicinal Chemistry
- Publisher
- American Chemical Society (ACS)
- Volume
- 69
- Issue
- 12
- Pages
- 14627–14646
- Publication date
- 8 June 2026
- Language
- EN