Synthesis of novel indeno[1,2-c]isoquinoline derivatives, functionalized at the D ring and bearing 1,2,3-triazole unit, has been reported. These hybrid compounds display cytotoxic activity against two human cancer cell lines – KB and HepG2 with half maximal inhibitory concentration (IC50) values in a range of 20–40 μM.
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The authors acknowledge the Vietnamese National Foundation for Science and Technology Development (grant 104.01-2017.27) for financial support.
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Published in Khimiya Geterotsiklicheskikh Soedinenii, 2020, 56(9), 1167–1172
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Pham, H.T., Le-Nhat-Thuy, G., Thi, T.A.D. et al. Synthesis and Evaluation of the Cytotoxicity of Indeno[1,2-c]Isoquinoline Derivatives Bearing Ester Functional Group and 1,2,3-Triazole Moiety. Chem Heterocycl Comp 56, 1167–1172 (2020). https://doi.org/10.1007/s10593-020-02792-4
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DOI: https://doi.org/10.1007/s10593-020-02792-4