article · Future Medicinal Chemistry

Design and synthesis of novel 3,5-diphenyl pyrazolines acting as potent EGFR inhibitors with off-target antileukemic effect

2025Open accessSinai University

Abstract

AIM: bearing the terminal piperidine or morpholine moieties commonly observed in clinically approved EGFR inhibitors were synthesized as novel anti-cancer agents acting via EGFR inhibition. MATERIALS & METHODS: anti-cancer activity against 60 NCI cell lines. RESULTS: are expected to be bioavailable and drug-like compounds. CONCLUSION: has off-target antileukemic effect.

Research topics

Synthesis and biological activity
Lung Cancer Treatments and Mutations
HER2/EGFR in Cancer Research

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DOI: 10.1080/17568919.2025.2559579

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