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| Title | Structure-Based Design of 4-(1-Methyl-1 H -indol-3-yl)pyrimidin-2-amine Derivatives as the First Covalent FGFR3 Selective Inhibitors. |
|---|---|
| Journal, issue, pages | J. Med. Chem., Vol. 69, Page 5199-5218, Year 2026 |
| Publish date | Jun 25, 2025 (structure data deposition date) |
Authors | Zhu, W. / Chen, X. / Li, X. / Lin, J. / Lin, X. / Liu, X. / Deng, W. / Song, X. / Tu, Z. / Patterson, A.V. ...Zhu, W. / Chen, X. / Li, X. / Lin, J. / Lin, X. / Liu, X. / Deng, W. / Song, X. / Tu, Z. / Patterson, A.V. / Smaill, J.B. / Chen, Y. / Lu, X. |
External links | J. Med. Chem. / PubMed:41648938 |
| Methods | X-ray diffraction |
| Resolution | 1.81 - 2.65 Å |
| Structure data | ![]() PDB-9vlj: ![]() PDB-9vlm: ![]() PDB-9vm9: ![]() PDB-9vmb: |
| Chemicals | ![]() PDB-1esp: ![]() ChemComp-SO4: ![]() ChemComp-HOH: ![]() ChemComp-GOL: ![]() PDB-1esw: ![]() ChemComp-MG: ![]() PDB-1esx: |
| Source |
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Keywords | TRANSFERASE / FGFR1 / FGFR2 / FGFR3 |
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homo sapiens (human)
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