Статья
2021
Synthesis of Triazolylisatins Glycoconjugates and Some Ammonium Hydrazones on Their Basis
A. V. Bogdanov, O. V. Andreeva, M. G. Belenok, A. D. Voloshina, K. I. Enikeeva, A. V. Samorodov, V. F. Mironov
Российский журнал общей химии
https://doi.org/10.1134/S1070363221070045
Abstract / Full Text
The click reaction of propargylisatins with some azido-sugars was used to synthesize new isatin derivatives, in which the carbohydrate residue is linked to the 2,3-dioxindole scaffold via the 1,2,3-triazole ring. A number of water-soluble acylhydrazones with various structure of cationic fragment were obtained on their basis. It was shown that the newly obtained compounds do not exhibit hemotoxic action and have a significant antiaggregatory and anticoagulant activity at the level of reference drugs such as acetylsalicylic acid and pentoxifylline.
Author information
- A.E. Arbuzov Institute of Organic and Physical Chemistry, Federal Research Center “Kazan Scientific Center of Russian Academy of Sciences”, 420088, Kazan, RussiaA. V. Bogdanov, O. V. Andreeva, M. G. Belenok, A. D. Voloshina & V. F. Mironov
- Bashkir State Medical University, 450000, Ufa, RussiaK. I. Enikeeva & A. V. Samorodov
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