@ARTICLE{Rusinov2015275,
author={Rusinov, V.L. and Sapozhnikova, I.M. and Ulomskii, E.N. and Medvedeva, N.R. and Egorov, V.V. and Kiselev, O.I. and Deeva, E.G. and Vasin, A.V. and Chupakhin, O.N.},
title={Nucleophilic substitution of nitro group in nitrotriazolotriazines as a model of potential interaction with cysteine-containing proteins},
journal={Chemistry of Heterocyclic Compounds},
year={2015},
volume={51},
number={3},
pages={275-280},
doi={10.1007/s10593-015-1695-4},
note={cited By 5},
url={https://www.scopus.com/inward/record.uri?eid=2-s2.0-84953354086&doi=10.1007%2fs10593-015-1695-4&partnerID=40&md5=d3ba1311a60e70bf3af9efa09f7884c4},
affiliation={Ural Federal University Named after the First President of Russia Boris Yeltsin, 19 Mira St., Yekaterinburg, 620002, Russian Federation; Institute of Organic Synthesis, Ural Branch, Russian Academy of Sciences, 22 S. Kovalevskoi St. / 20 Akademicheskaya St., Yekaterinburg, 620990, Russian Federation; Research Institute of Influenza, Ministry of Healthcare of the Russian Federation, 15/17 Prof. Popov St., Saint-Petersburg, 197376, Russian Federation},
abstract={[Figure not available: see fulltext.] 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. © 2015 Springer Science+Business Media New York.},
author_keywords={azolo[5,1-c]triazines;  cysteine;  glutathione;  metabolic transformations;  nitro compounds;  nucleophilic substitution;  Triazavirin},
correspondence_address1={Sapozhnikova, I.M.; Ural Federal University Named after the First President of Russia Boris Yeltsin, 19 Mira St., Russian Federation; email: i.m.sapozhnikova@urfu.ru},
publisher={Springer New York LLC},
issn={00093122},
coden={CHCCA},
language={English},
abbrev_source_title={Chem. Heterocycl. Compd.},
document_type={Article},
source={Scopus},
}

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Heterocycl. Compd.","document_type":"Article","source":"Scopus","bibtex":"@ARTICLE{Rusinov2015275,\r\nauthor={Rusinov, V.L. and Sapozhnikova, I.M. and Ulomskii, E.N. and Medvedeva, N.R. and Egorov, V.V. and Kiselev, O.I. and Deeva, E.G. and Vasin, A.V. and Chupakhin, O.N.},\r\ntitle={Nucleophilic substitution of nitro group in nitrotriazolotriazines as a model of potential interaction with cysteine-containing proteins},\r\njournal={Chemistry of Heterocyclic Compounds},\r\nyear={2015},\r\nvolume={51},\r\nnumber={3},\r\npages={275-280},\r\ndoi={10.1007/s10593-015-1695-4},\r\nnote={cited By 5},\r\nurl={https://www.scopus.com/inward/record.uri?eid=2-s2.0-84953354086&doi=10.1007%2fs10593-015-1695-4&partnerID=40&md5=d3ba1311a60e70bf3af9efa09f7884c4},\r\naffiliation={Ural Federal University Named after the First President of Russia Boris Yeltsin, 19 Mira St., Yekaterinburg, 620002, Russian Federation; Institute of Organic Synthesis, Ural Branch, Russian Academy of Sciences, 22 S. 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