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7VRE

The crystal structure of EGFR T790M/C797S with the inhibitor HCD2892

Summary for 7VRE
Entry DOI10.2210/pdb7vre/pdb
DescriptorEpidermal growth factor receptor, 5-chloranyl-N-[5-chloranyl-2-methoxy-4-[4-(4-methylpiperazin-1-yl)piperidin-1-yl]phenyl]-4-(1-ethylsulfonylindol-3-yl)pyrimidin-2-amine (3 entities in total)
Functional Keywordsegfr, inhibitor, complex, transferase, transferase-transferase inhibitor complex, transferase/transferase inhibitor
Biological sourceHomo sapiens (Human)
Total number of polymer chains1
Total formula weight38119.00
Authors
Zhu, S.J. (deposition date: 2021-10-22, release date: 2022-06-08, Last modification date: 2023-11-29)
Primary citationChen, H.,Lai, M.,Zhang, T.,Chen, Y.,Tong, L.,Zhu, S.,Zhou, Y.,Ren, X.,Ding, J.,Xie, H.,Lu, X.,Ding, K.
Conformational Constrained 4-(1-Sulfonyl-3-indol)yl-2-phenylaminopyrimidine Derivatives as New Fourth-Generation Epidermal Growth Factor Receptor Inhibitors Targeting T790M/C797S Mutations.
J.Med.Chem., 65:6840-6858, 2022
Cited by
PubMed: 35446588
DOI: 10.1021/acs.jmedchem.2c00168
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.507 Å)
Structure validation

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