Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Evsey A. Ruchko"'
Autor:
Dmitry S. Sheikin, Evgeniya S. Titova, Evsey А. Ruchko, Maxim B. Nawrozkij, Anastasiya Kotlyarova, Ivan А. Novakov, Leila L. Brunilina, Tatyana G. Tolstikova, Alla Pavlova, Ivan А. Kirillov, Mariya D. Robinovich
Publikováno v:
Chemistry of Heterocyclic Compounds. 56:769-775
New structural analogs of 3-phenacyluridine were obtained as a result of N(3)-alkylation of 1-(2-acetoxyethyl)- and 1-(2-acetoxyethoxymethyl) uracil. Biological studies of the title compounds in an acute in vivo experiment did not reveal their hypnot
Autor:
Dmitry S. Sheikin, A. Yu. Maryshev, A. S. Babushkin, Dominique Schols, V. V. Chapurkin, Ivan A. Novakov, M. B. Navrotskii, Evsey A. Ruchko
Publikováno v:
Russian Journal of General Chemistry. 90:352-356
The Tscherniac–Einhorn reaction of 6-methyl and 6-(trifluoromethyl) derivatives of 2-thiouracil with N-(bromomethyl)phthalimide in under basic catalysis leads to the formation of S-amidomethylation products. When using 6-amino-2-thiouracil, decompo
Autor:
Evsey A. Ruchko, Vladimir Egorovich Fedorov, Anton Vladimirovich Omelkov, Pharm-Synthesis\\', Jsc \\'Pharm-Synthesis\\'
Publikováno v:
Butlerov Communications. 61:21-32
The discovery in 2002 among derivatives of 6-bromo-3-benzyl-2-methoxyquinolines the highly active compounds against M. Tuberculosis bacterium and its drug-resistant strains led to the creation of the innovative anti-TB drug TMS-207 in 2013 by Janssen
Autor:
Anton Yu. Maryshev, Viktor V. Chapurkin, Dmitry S. Sheikin, Dominique Schols, Yaroslav P. Kuznetsov, Maksim B. Nawrozkij, Ivan A. Novakov, Alexande S. Babushkin, Evsey A. Ruchko, Vadim V. Kachala
Publikováno v:
Chemistry of Heterocyclic Compounds. 56:67-72
The interaction of N-(2-bromoethyl)- and N-(3-bromopropyl)phthalimides with 2-thiouracils substituted at position 6 was studied in alkaline medium, providing S-monoamidoalkylation products and, depending on the substituents, the products of S,O(4)- a
Autor:
L. L. Brunilina, V. V. Chapurkin, Evsey A. Ruchko, Dmitry S. Sheikin, Dominique Schols, Y. P. Kuznetsov, I. A. Novakov, M. B. Nawrozkij
Publikováno v:
AIP Conference Proceedings.
Synthesis of the novel Isothiobarbamine analogues with lowered basicity has been prepared. The peculiarities of their synthesis and preliminary data on their biological activity are presented.
Autor:
Maksim B. Nawrozkij, Alexandre S. Babushkin, Vadim V. Kachala, Dominique Schols, Sergey N. Lavrenov, Evsey A. Ruchko
Publikováno v:
Chemistry of Heterocyclic Compounds. 51:978-983
We report new carboanalogs of umifenovir – regioisomeric derivatives of ethyl 5-hydroxy-(trans-2-phenylcyclopropyl)-1Н-indole-3-carboxylate. The inhibition of HIV replication by umifenovir and its carboanalogs at micromolar concentration range has
Autor:
Ivan A. Novakov, M. B. Nawrozkij, V. N. Charushin, Evgeniy B. Gorbunov, G. L. Rusinov, Alexandre S. Babushkin, Evsey A. Ruchko
Publikováno v:
Macroheterocycles
A convenient way to 1-(pyridin-2-yl)ethan-1,2-diol, 2-(oxiran-2-yl)pyridine and two diastereomeric forms of 1-(piperidin-2-yl)ethan-1,2-diol, valuable building-blocks for the synthesis of functionalized crown ethers, has been developed. It is based o
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