@article{2021-09-16,
author = {, , , , , , },
title = {},
year = {2021},
doi = {10.1134/S1070363221070045},
publisher = {NP «NEICON»},
abstract = {Abstract: 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. [Figure not available: see fulltext.]. © 2021, Pleiades Publishing, Ltd.},
URL = {https://repo.bashgmu.ru/publication/1660},
eprint = {https://repo.bashgmu.ru/files/1831},
}