Author:
Mohamed Magda F.,Ibrahim Nada S.,Saddiq Amna A.,Abdelhamid Ismail A.
Abstract
AbstractA novel series of α-cyano indolylchalcones was prepared, and their chemical structures were confirmed based on the different spectral data. Among them, compound 7f was observed to be the most effective bioactive chalcone with distinguished potency and selectivity against colorectal carcinoma (HCT116) with IC50 value (6.76 µg/mL) relative to the positive control (5 FU) (77.15 µg/mL). In a preliminary action study, the acrylonitrile chalcone 7f was found to enhance apoptotic action via different mechanisms like inhibition of some anti-apoptotic protein expression, regulation of some apoptotic proteins, production of caspases, and cell cycle arrest. All mechanisms suggested that compound 7f could act as a professional chemotherapeutic agent. Also, a molecular docking study was achieved on some selected proteins implicated in cancer (Caspase 9, XIAP, P53 mutant Y220C, and MDM2) which showed variable interactions with compound 7f with good Gibbs free energy scores.
Publisher
Springer Science and Business Media LLC
Reference92 articles.
1. Faubert, B., Solmonson, A. & DeBerardinis, R. J. Metabolic reprogramming and cancer progression. Science 368, 1–10 (2020).
2. Plass, C. et al. Mutations in regulators of the epigenome and their connections to global chromatin patterns in cancer. Nat. Rev. Genet. 14, 765–780 (2013).
3. Erturk, E., Tuna, G., Coskun, D. & Ari, F. Investigation of anti-cancer activity of newly synthesized 2,4-pentadien-1-one derivative containing benzofuran in human lung and colon cancer cells. Eurasian J. Med. Oncol. 7, 24–33 (2023).
4. Song, J. J. et al. Construction of the indole nucleus through C-H functionalization reactions. Arkivoc 2010, 390–449 (2010).
5. Shiri, M. Indoles in multicomponent processes (MCPs). Chem. Rev. 112, 3508–3549 (2012).
Cited by
4 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献