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Updated: May 20, 2026

Functionalized Spirocyclic Heterocycle Synthesis and Cytotoxicity Assay
Published on: February 9, 2021
Conformationally-restricted cyclic sulfones as potent and selective mTOR kinase inhibitors
Kevin K-C Liu1, Simon Bailey, Dac M Dinh
1Pfizer Global Research and Development, Chemistry Department, La Jolla, CA 92120, USA. Liu_Kang_Zhi_Kevin@Lilly.com
Abstract:
Novel conformationally-restricted mTOR kinase inhibitors with cyclic sulfone scaffold were designed. Synthesis and structure-activity relationship (SAR) studies are described with emphasis on optimization of the mTOR potency and selectivity against class I PI3Kα kinase. PF-05139962 was identified with excellent mTOR biochemical inhibition, cellular potency, kinase selectivity and in vitro ADME properties.
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