Development of a Potent Brain-Penetrant EGFR Tyrosine Kinase Inhibitor against Malignant Brain Tumors

• Published in: ACS medicinal chemistry letters Vol. 11; no. 10; pp. 1799 - 1809
• Main Authors: Tsang, Jonathan E, Urner, Lorenz M, Kim, Gyudong, Chow, Kingsley, Baufeld, Lynn, Faull, Kym, Cloughesy, Timothy F, Clark, Peter M, Jung, Michael E, Nathanson, David A
• Format: Journal Article
• Language: English
• Published: WASHINGTON American Chemical Society 08.10.2020; Amer Chemical Soc
• Subjects: Chemistry, Medicinal; Innovations; Life Sciences & Biomedicine; Pharmacology & Pharmacy; Science & Technology; EGFRvIII; brain-penetration; kinase inhibitor; glioblastoma; EGFR; RECOGNITION; NSCLC; FAMILY; FACTOR RECEPTOR EGFR; METABOLISM; FLUORINE; 4-ANILINOQUINAZOLINE; ERLOTINIB
• ISSN: 1948-5875; 1948-5875
• DOI: 10.1021/acsmedchemlett.9b00599

The epidermal growth factor receptor (EGFR) is genetically altered in nearly 60% of glioblastoma tumors; however, tyrosine kinase inhibitors (TKIs) against EGFR have failed to show efficacy for patients with these lethal brain tumors. This failure is attributed to the inability of clinically tested EGFR TKIs to cross the blood–brain barrier (BBB) and achieve adequate pharmacological levels to inhibit various oncogenic forms of EGFR that drive glioblastoma. Through SAR analysis, we developed compound 5 (JCN037) from an anilinoquinazoline scaffold by ring fusion of the 6,7-dialkoxy groups to reduce the number of rotatable bonds and polar surface area and by introduction of an ortho-fluorine and meta-bromine on the aniline ring for improved potency and BBB penetration. Relative to the conventional EGFR TKIs erlotinib and lapatinib, JCN037 displayed potent activity against EGFR amplified/mutant patient-derived cell cultures, significant BBB penetration (2:1 brain-to-plasma ratio), and superior efficacy in an EGFR-driven orthotopic glioblastoma xenograft model.