Convenient synthesis and X-ray determination of 2-amino-6H-1,3,4-thiadiazin-3-ium bromides endowed with antiproliferative activity

HN Tawfeek, Alshaimaa Abdelmoez, Kholood A. Dahlous, Bahaa G. M. Youssif, Stefan Bräse, K Rissanen, M Nieger, Essmat M. El-Sheref

Forskningsoutput: KonferensbidragKonferenspapperPeer review

Sammanfattning

A new series of 1,3,4-thiadiazin-3-ium bromide derivatives 9a-g were prepared as a six-member ring by interactions between 4-substituted thiosemicarbazides 8a-e and alpha-halo ketones 2a,b. The reaction was conducted using hydrazine-NH2 and yielded a hexagonal shape. The structures of all obtained compounds have been verified using IR, NMR spectra, mass spectrometry, elemental analysis, and X-ray crystallography. The X-ray crystallographic analysis of compounds 9a and 9b has revealed that the salt is formed with the nitrogen atom N(3 )when the aromatic substituents 9a and 9d are present, but in the case of compounds 9b, 9c, 9e, 9f, and 9g with the aliphatic substituent, the salt is formed outside the ring. Compounds 9a-g were evaluated for antiproliferative activity as multitargeted inhibitors. Results revealed that targets 9a-g displayed good antiproliferative activity, with GI50 ranging from 38 nM to 66 nM against a panel of four cancer cell lines compared to the reference Erlotinib (GI(50 )= 33 nM). Compounds 9a, 9c, and 9d were the most potent antiproliferative derivatives, with GI(50 )values of 43, 38, and 47 nM, respectively. Compounds 9a, 9c, and 9d were evaluated for their inhibitory activity against EGFR, BRAF(V600E), and VEGFR-2. The in vitro experiments demonstrated that the compounds being examined exhibit potent antiproliferative properties and have the potential to function as multitargeted inhibitors. In addition, the western blotting investigation demonstrated the inhibitory effects of 9c on EGFR, BRAF(V600E), and VEGFR-2.
Originalspråkengelska
Sidor17866-17876
Antal sidor11
DOI
StatusPublicerad - 28 maj 2024
MoE-publikationstypEj behörig

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