NUCLEOPHILIC SUBSTITUTION OF NITRO GROUP IN NITROTRIAZOLO- TRIAZINES AS A MODEL OF POTENTIAL INTERACTION WITH CYSTEINE-CONTAINING PROTEINS
DOI:
https://doi.org/10.1007/2244Keywords:
azolo[5, 1-с]triazines, cysteine, glutathione, nitro compounds, Triazavirin, metabolic transformations, , nucleophilic substitutionAbstract
The nucleophilic susbstitution of nitro group in [1,2,4]triazolo[5,1-c][1,2,4]triazinones upon treatment with cysteine and glutathione was studied as a model for the interaction with thiol groups of virus proteins, which mimics the metabolic transformations of antiviral drug Triazavirin® and its derivatives.
How to Cite
Rusinov, V. L.; Sapozhnikova, I. M.; Ulomskii, E. N.; Medvedeva, N. R.; Egorov, V. V.; Kiselev, O. I.; Deeva, E. G.; Vasin, A. V.; Chupakhin, O. N. Chem. Heterocycl. Compd. 2015, 51, 275. [Khim. Geterotsikl. Soedin. 2015, 51, 275.]
For this article in the English edition see DOI 10.1007/s10593-015-1695-4