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8Y22

FGFR1 kinase domain with a covalent inhibitor 9g

This is a non-PDB format compatible entry.
Summary for 8Y22
Entry DOI10.2210/pdb8y22/pdb
DescriptorFibroblast growth factor receptor 1, ~{N}-[4-[[4-azanyl-3-(7-methoxy-5-methyl-1-benzothiophen-2-yl)pyrazolo[3,4-d]pyrimidin-1-yl]methyl]phenyl]propanamide, SULFATE ION, ... (4 entities in total)
Functional Keywordsfibroblast growth factor receptor 1, transferase
Biological sourceHomo sapiens (human)
Total number of polymer chains2
Total formula weight71838.27
Authors
Chen, X.J.,Chen, Y.H. (deposition date: 2024-01-25, release date: 2024-06-26)
Primary citationDeng, W.,Chen, X.,Liang, H.,Song, X.,Xiang, S.,Guo, J.,Tu, Z.,Zhou, Y.,Chen, Y.,Lu, X.
Design, synthesis and biological evaluation of 5-amino-1H-pyrazole-4-carboxamide derivatives as pan-FGFR covalent inhibitors.
Eur.J.Med.Chem., 275:116558-116558, 2024
Cited by
PubMed: 38870833
DOI: 10.1016/j.ejmech.2024.116558
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.792 Å)
Structure validation

222624

數據於2024-07-17公開中

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