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11HQ

Type-III c-MET Inhibitor Enabled by Free-Energy Perturbation Calculations

This is a non-PDB format compatible entry.
Summary for 11HQ
Entry DOI10.2210/pdb11hq/pdb
DescriptorHepatocyte growth factor receptor, (1R,6M)-1-benzyl-6-[(3P)-3-(1-ethyl-1H-pyrazol-4-yl)-5-fluorophenyl]-1,2-dihydro-3H-pyrrolo[3,4-c]pyridin-3-one (3 entities in total)
Functional Keywordstyrosine kinase, transferase
Biological sourceHomo sapiens (human)
Total number of polymer chains3
Total formula weight105983.48
Authors
Eiler, D.R.,Abraham, N.,Kutter, S.,Kroeck, K.G. (deposition date: 2026-02-25, release date: 2026-05-27)
Primary citationTherrien, E.,Feng, S.,Amberg-Johnson, K.,Shaikh, N.,Patil, P.,Majumdar, S.,Abraham, N.,Eiler, D.,Kutter, S.,Albanese, S.K.,Haldar, S.,Kroeck, K.G.,Atsriku, C.,Gerasyuto, A.I.,Levinson, A.M.
Discovery of 2H-Pyrrolo[3,4-c]pyridin-3-one Derivatives as Type-III c-MET Inhibitors Enabled by Free-Energy Perturbation Calculations
Acs Med.Chem.Lett., 2026
Cited by
DOI: 10.1021/acsmedchemlett.6c00158
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.65 Å)
Structure validation

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PDB entries from 2026-06-10

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