Dual Kit/Aur Inhibitors as Chemosensitizing Agents for the Treatment of Melanoma: Design, Synthesis, Docking Studies and Functional Investigation

Luca Quattrini, Vito Coviello, Stefania Sartini, Teresa Di Desidero, Paola Orlandi, Yi Yu Ke, Kai Lun Liu, Hsing Pang Hsieh, Guido Bocci, Concettina La Motta

研究成果: Article同行評審

1 引文 斯高帕斯(Scopus)

摘要

Melanoma is the most serious form of skin cancer but its medication is still far from being safe and thoroughly effective. The search of novel therapeutic approaches represents therefore a health emergency to push through eagerly. In this study, we describe a novel class of dual c-Kit/Aur inhibitors, characterized by a 1,2,4-triazole core and developed by a structure-based optimization of a previously developed hit, and report the evidence of their significance as drug candidates for the treatment of melanoma. Compound 6a, merging the best inhibitory profile against the target kinases, showed anti-proliferative efficacy against the human melanoma cell lines A2058, expressing the BRAF V600D mutation, and WM266-4, expressing BRAF V600E. Significantly, it displayed also a highly synergistic profile when tested in combination with vemurafenib, thus proving its efficacy not only per se but even in a combination therapy, which is nowadays acknowledged as the cornerstone approach of the forthcoming tumour management.

原文English
文章編號9943
期刊Scientific reports
9
發行號1
DOIs
出版狀態Published - 2019 十二月 1

All Science Journal Classification (ASJC) codes

  • General

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