7Y4T
Crystal structure of cMET kinase domain bound by compound 9I
Summary for 7Y4T
Entry DOI | 10.2210/pdb7y4t/pdb |
Descriptor | Hepatocyte growth factor receptor, 2-[2-[3-(1-methylpyrazol-4-yl)quinolin-6-yl]ethyl]-6-(3-nitrophenyl)pyridazin-3-one (3 entities in total) |
Functional Keywords | transferase inhibitor, transferase, transferase-inhibitor complex, transferase/inhibitor |
Biological source | Homo sapiens (human) |
Total number of polymer chains | 1 |
Total formula weight | 35294.78 |
Authors | Qu, L.Z.,Chen, Y.H. (deposition date: 2022-06-16, release date: 2022-11-23, Last modification date: 2023-11-29) |
Primary citation | Wang, C.,Li, J.,Qu, L.,Tang, X.,Song, X.,Yang, F.,Chen, X.,Lin, Q.,Lin, W.,Zhou, Y.,Tu, Z.,Chen, Y.,Zhang, Z.,Lu, X. Discovery of D6808, a Highly Selective and Potent Macrocyclic c-Met Inhibitor for Gastric Cancer Harboring MET Gene Alteration Treatment. J.Med.Chem., 65:15140-15164, 2022 Cited by PubMed: 36355693DOI: 10.1021/acs.jmedchem.2c00981 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.16 Å) |
Structure validation
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