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Discovery of mobocertinib, a potent, oral inhibitor of EGFR exon 20 insertion mutations in non-small cell lung cancer.

Abstract
In the treatment of non-small cell lung cancer (NSCLC), patients harboring exon 20 insertion mutations in the epidermal growth factor receptor (EGFR) gene (EGFR) have few effective therapies because this subset of mutants is generally resistant to most currently approved EGFR inhibitors. This report describes the structure-guided design of a novel series of potent, irreversible inhibitors of EGFR exon 20 insertion mutations, including the V769_D770insASV and D770_N771insSVD mutants. Extensive structure-activity relationship (SAR) studies led to the discovery of mobocertinib (compound 21c), which inhibited growth of Ba/F3 cells expressing the ASV insertion with a half-maximal inhibitory concentration of 11 nM and with selectivity over wild-type EGFR. Daily oral administration of mobocertinib induced tumor regression in a Ba/F3 ASV xenograft mouse model at well-tolerated doses. Mobocertinib was approved in September 2021 for the treatment of adult patients with advanced NSCLC with EGFR exon 20 insertion mutations with progression on or after platinum-based chemotherapy.
AuthorsWei-Sheng Huang, Feng Li, Yongjin Gong, Yun Zhang, Willmen Youngsaye, Yongjin Xu, Xiaotian Zhu, Matthew T Greenfield, Anna Kohlmann, Paul M Taslimi, Angela Toms, Stephan G Zech, Tianjun Zhou, Biplab Das, Hyun G Jang, Meera Tugnait, Yihua E Ye, Francois Gonzalvez, Theresa E Baker, Sara Nadworny, Yaoyu Ning, Scott D Wardwell, Sen Zhang, Alexandra E Gould, Yongbo Hu, Weston Lane, Robert J Skene, Hua Zou, Tim Clackson, Narayana I Narasimhan, Victor M Rivera, David C Dalgarno, William C Shakespeare
JournalBioorganic & medicinal chemistry letters (Bioorg Med Chem Lett) Vol. 80 Pg. 129084 (01 15 2023) ISSN: 1464-3405 [Electronic] England
PMID36423823 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2022 The Authors. Published by Elsevier Ltd.. All rights reserved.
Chemical References
  • mobocertinib
  • ErbB Receptors
  • Protein Kinase Inhibitors
  • EGFR protein, human
Topics
  • Humans
  • Mice
  • Animals
  • Carcinoma, Non-Small-Cell Lung (drug therapy, genetics, pathology)
  • Lung Neoplasms (drug therapy, genetics, pathology)
  • Mutagenesis, Insertional
  • Mutation
  • ErbB Receptors
  • Exons
  • Protein Kinase Inhibitors (pharmacology, therapeutic use)

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