Development and In Vivo Evaluation of Fused Benzazole Analogs of Anti-Melanoma Agent HA15

Background: In line with our recent discovery of an efficient anticancer thiazolebenzenesulfonamide framework HA15 (1) based on a remarkable endoplasmic reticulum stress inducement mode of action, we report herein a series of innovative constrained HA15 analogs, featuring four types of bicylic deriv...

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Veröffentlicht in:Future medicinal chemistry 2021-07, Vol.13 (14), p.1157-1173
Hauptverfasser: Millet, Antoine, Filho, Mauro Safir, Hamouda-Tekaya, Nedra, Cavazza, Elisa, Abbe, Patricia, Rüdiger, Johanna, Plaisant, Magali, Mayen, Julie, Rocchi, Stéphane, Ronco, Cyril, Benhida, Rachid
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Sprache:eng
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Zusammenfassung:Background: In line with our recent discovery of an efficient anticancer thiazolebenzenesulfonamide framework HA15 (1) based on a remarkable endoplasmic reticulum stress inducement mode of action, we report herein a series of innovative constrained HA15 analogs, featuring four types of bicylic derivatives. Results: The structure–activity relationship analysis, using a cell line assay, led us to identify a novel version of HA15: a new benzothiazole derivative (10b) exhibiting important anti-melanoma effect against sensitive and resistant melanoma cells. Meanwhile, compound 10b induced a significant tumor growth inhibition in vivo with no apparent signs of toxicity. Conclusion: These results consistently open new directions to improve and develop more powerful anticancer therapeutics harboring this type of fused framework.
ISSN:1756-8919
1756-8927
DOI:10.4155/fmc-2021-0001