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Al-Salem, Huda S; Arifuzzaman, Md; Alkahtani, Hamad M; Abdalla, Ashraf N; Issa, Iman S; Alqathama, Aljawharah; Albalawi, Fatemah S; Rahman, A F M Motiur
Molecules (Basel, Switzerland), 09/2020, Volume: 25, Issue: 19Journal Article
Isatin derivatives potentially act on various biological targets. In this article, a series of novel isatin-hydrazones were synthesized in excellent yields. Their cytotoxicity was tested against human breast adenocarcinoma (MCF7) and human ovary adenocarcinoma (A2780) cell lines using MTT assay. Compounds (IC = 1.51 ± 0.09 µM) and (IC = 3.56 ± 0.31) showed excellent activity against MCF7, whereas compound showed considerable cytotoxicity against both tested cell lines, MCF7 (IC = 5.46 ± 0.71 µM) and A2780 (IC = 18.96± 2.52 µM), respectively. Structure-activity relationships (SARs) revealed that, halogen substituents at 2,6-position of the C-ring of isatin-hydrazones are the most potent derivatives. In-silico absorption, distribution, metabolism and excretion (ADME) results demonstrated recommended drug likeness properties. Compounds (IC = 0.245 µM) and (IC = 0.300 µM) exhibited good inhibitory activity against the cell cycle regulator CDK2 protein kinase compared to imatinib (IC = 0.131 µM). A molecular docking study of and confirmed both compounds as type II ATP competitive inhibitors that made interactions with ATP binding pocket residues, as well as lacking interactions with active state DFG motif residues.
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