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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2023 Volume 33, Issue 1, Pages 73–76 (Mi mendc312)

This article is cited in 6 papers

Communications

2-Amino-4-(aminomethyl)thiazole-based derivatives as potential antitumor agents: design, synthesis, cytotoxicity and apoptosis inducing activities

M. Liaoa, D. Huangab, Y.-X. Chengab

a School of Pharmaceutical Sciences, Health Science Center, Shenzhen University, Shenzhen, China
b Institute for Inheritance-Based Innovation of Chinese Medicine, School of Pharmaceutical Sciences, Health Science Center, Shenzhen University, Shenzhen, China

Abstract: Novel 2-amino-4-(aminomethyl)thiazole derivatives were designed and synthesized by a facile method including the Hantzsch construction of thiazole core followed by amidation and nucleophilic substitution steps. Bioassay results showed that 4-(tert-butyl)-N-[4-(piperazin-1-ylmethyl)thiazol-2-yl]-benzamide and 4-(tert-butyl)-N-{4-[(4-piperidinopiperidin-1-yl)methyl]thiazol-2-yl}benzamide possessed similar activities compared with 5-fluorouracil. The 4-piperidino-piperidin-1-yl-containing derivative also suppressed proliferation of cultured tumor cells by inducing apoptosis.

Keywords: thiazole derivatives, antitumor, drug design, Hantzsch reaction, amidation, structure–activity relationship, apoptosis.

Language: English

DOI: 10.1016/j.mencom.2023.01.023



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