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Updated: May 8, 2026

In Vitro Chemical Mapping of G-Quadruplex DNA Structures by Bis-3-Chloropiperidines
Published on: May 12, 2023
Optimization of anti-proliferative activity using a screening approach with a series of bis-heterocyclic G-quadruplex
Stephan A Ohnmacht1, Cristina Ciancimino, Giulia Vignaroli
1UCL School of Pharmacy, University College London, London, UK.
Abstract:
Using a phenotypic screening and SAR optimization approach, a phenyl-bis-oxazole derivative has been identified with anti-proliferative activity, optimized with the use of a panel of cancer cell lines. The lead compound was synthesized by means of a short and effective two-step synthesis using Pd-catalyzed direct arylation. The compound stabilizes several quadruplex DNA sequences including a human telomeric DNA and one from the promoter of the HSP90 gene, although the structure-activity relationships of the series are not obviously related to the quadruplex binding.

