Cytotoxic evaluation of original pyrazolo[3,4-d]thiazoles and pyrazolo[3,4-c]pyrazoles - Archive ouverte HAL Access content directly
Journal Articles Farmacia Year : 2022

Cytotoxic evaluation of original pyrazolo[3,4-d]thiazoles and pyrazolo[3,4-c]pyrazoles

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Abstract

A concise and versatile synthetic strategy for the synthesis of original substituted heterobicycles was developed, relying on the use of aromatic hydrazines in one-pot condensations and Ullmann-type intramolecular cyclization sequences, as well as on chemoselective brominations and palladium-mediated cross-coupling reactions. In this study, the two series of novel heterobicycles were tested for their cytotoxic potential. The compounds were structurally characterized by nuclear magnetic resonance spectrometry (1H NMR and 13C NMR), infrared spectroscopy (IR) and high-resolution mass spectrometry (HRMS). The IC50 values of these compounds on five tumour cell lines (A-549, HS-683, MCF-7, SK-MEL-28 and B16-F1) were obtained by MTT colorimetric assay. Six of the compounds exhibited excellent activity compared to 5-fluorouracil against two of the five cell lines tested, with IC50 values ranging from 0.1 to 10 μM.

Dates and versions

hal-03890855 , version 1 (08-12-2022)

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Nicu-Cosmin Ostache, Arnaud Pâris, Marie-Aude Hiebel, Adriana-Luminita Fînaru, Richard Daniellou, et al.. Cytotoxic evaluation of original pyrazolo[3,4-d]thiazoles and pyrazolo[3,4-c]pyrazoles. Farmacia, 2022, 70 (2), pp.258-265. ⟨10.31925/farmacia.2022.2.10⟩. ⟨hal-03890855⟩
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