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ЖУРНАЛЫ // Mendeleev Communications // Архив

Mendeleev Commun., 2023, том 33, выпуск 1, страницы 73–76 (Mi mendc312)

Эта публикация цитируется в 6 статьях

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


Аннотация: 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.

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

Язык публикации: английский

DOI: 10.1016/j.mencom.2023.01.023



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