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8UDT

The X-RAY co-crystal structure of human FGFR3 and KIN-3248

Summary for 8UDT
Entry DOI10.2210/pdb8udt/pdb
DescriptorFibroblast growth factor receptor 3, D-MALATE, 3-[(1-cyclopropyl-4,6-difluoro-1H-benzimidazol-5-yl)ethynyl]-1-[(3R,5R)-5-(methoxymethyl)-1-propanoylpyrrolidin-3-yl]-5-(methylamino)-1H-pyrazole-4-carboxamide, ... (4 entities in total)
Functional Keywordsfgfr inhibitor, covalent drug, kin-3248, alteration, mutation, structure-based drug design, kinase inhibitor, signaling, proliferation, transferase, transferase-inhibitor complex, transferase/inhibitor
Biological sourceHomo sapiens (human)
Total number of polymer chains3
Total formula weight103070.87
Authors
Primary citationTyhonas, J.S.,Arnold, L.D.,Cox, J.M.,Franovic, A.,Gardiner, E.,Grandinetti, K.,Kania, R.,Kanouni, T.,Lardy, M.,Li, C.,Martin, E.S.,Miller, N.,Mohan, A.,Murphy, E.A.,Perez, M.,Soroceanu, L.,Timple, N.,Uryu, S.,Womble, S.,Kaldor, S.W.
Discovery of KIN-3248, An Irreversible, Next Generation FGFR Inhibitor for the Treatment of Advanced Tumors Harboring FGFR2 and/or FGFR3 Gene Alterations.
J.Med.Chem., 67:1734-1746, 2024
Cited by
PubMed: 38267212
DOI: 10.1021/acs.jmedchem.3c01819
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.829 Å)
Structure validation

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