Start Selective and Rigidify: The Discovery Path toward a Next Generation of EGFR Tyrosine Kinase Inhibitors.
Animals
Antineoplastic Agents
/ chemistry
Benzimidazoles
/ chemistry
Carcinoma, Non-Small-Cell Lung
/ drug therapy
Cell Line, Tumor
Crystallography, X-Ray
Cyclization
Entropy
ErbB Receptors
/ antagonists & inhibitors
Female
Hepatocytes
Humans
Lung Neoplasms
/ drug therapy
Mice
Mice, Transgenic
Mutation
Protein Conformation
Protein Kinase Inhibitors
/ chemistry
Structure-Activity Relationship
Xenograft Model Antitumor Assays
Journal
Journal of medicinal chemistry
ISSN: 1520-4804
Titre abrégé: J Med Chem
Pays: United States
ID NLM: 9716531
Informations de publication
Date de publication:
27 11 2019
27 11 2019
Historique:
pubmed:
7
11
2019
medline:
15
7
2020
entrez:
6
11
2019
Statut:
ppublish
Résumé
The epidermal growth factor receptor (EGFR), when carrying an activating mutation like del19 or L858R, acts as an oncogenic driver in a subset of lung tumors. While tumor responses to tyrosine kinase inhibitors (TKIs) are accompanied by marked tumor shrinkage, the response is usually not durable. Most patients relapse within two years of therapy often due to acquisition of an additional mutation in EGFR kinase domain that confers resistance to TKIs. Crucially, oncogenic EGFR harboring both resistance mutations, T790M and C797S, can no longer be inhibited by currently approved EGFR TKIs. Here, we describe the discovery of
Identifiants
pubmed: 31689114
doi: 10.1021/acs.jmedchem.9b01169
doi:
Substances chimiques
Antineoplastic Agents
0
Benzimidazoles
0
Protein Kinase Inhibitors
0
benzimidazole
E24GX49LD8
EGFR protein, human
EC 2.7.10.1
ErbB Receptors
EC 2.7.10.1
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM