Bingül, MuratArndt, Greg M.Marshall, Glenn M.St. Black, David C.C.Cheung, BelamyKumar, Naresh Sampath2022-03-112022-03-112021Bingül, M., Arndt, G. M., Marshall, G. M., St. Black, D. C.C., Cheung, B. ve Kumar, N. S. (2021). Synthesis and characterisation of novel tricyclic and tetracyclic furoindoles: Biological evaluation as SAHA enhancer against neuroblastoma and breast cancer cells. Molecules, 26(19), 5745.1420-3049https://www.mdpi.com/1420-3049/26/19/5745https://hdl.handle.net/11468/9387PMID: 34641289WOS:000708237400001The dihydropyranoindole structures were previously identified as promising scaffolds for improving the anti-cancer activity of histone deacetylase inhibitors. This work describes the synthesis of related furoindoles and their ability to synergize with suberoylanilide hydroxamic acid (SAHA) against neuroblastoma and breast cancer cells. The nucleophilic substitution of hydroxyin-dole methyl esters with α-haloketones yielded the corresponding arylether ketones, which were subsequently cyclized to tricyclic and tetracyclic furoindoles. The furoindoles showed promising individual cytotoxic efficiency against breast cancer cells, as well as decent SAHA enhancement against cancer cells in select cases. Interestingly, the best IC50 value was obtained with the non-cyclized intermediate.eninfo:eu-repo/semantics/openAccessBreast cancerFuroindoleHDAC inhibitorsNeuroblastomaSAHA enhancementArticle26195745WOS:0007082374000012-s2.0-851157259373464128910.3390/molecules26195745Q1Q2