Zobrazeno 1 - 10
of 29
pro vyhledávání: '"S M, Vinogradova"'
Autor:
S. M. Vinogradova, I. S. Silin
Publikováno v:
Humanitarian Vector. 12:79-87
Autor:
Yu. N. Sheinker, K. F. Turchin, M. D. Mashkovskii, I. V. Golovanova, O. S. Anisimova, S. M. Vinogradova, A. P. Pleshkova, S. D. Yuzhakov
Publikováno v:
Pharmaceutical Chemistry Journal. 31:224-228
Autor:
S. D. Sokolov, O. S. Anisimova, O. G. Azarevich, S. D. Yuzhakov, M. V. Berg, K. F. Turchin, M. D. Mashkovskii, S. M. Vinogradova
Publikováno v:
Pharmaceutical Chemistry Journal. 29:119-123
Novel 3-amino-2-hydroxypropoxy derivatives of 5-phenoxymethyl-1,2,4-oxadiazole were synthesized. Compounds were discovered among them that had pronounced Β-adrenergic blocking activity combined with moderate α-adrenergic blocking properties.
[Study of the antiviral activity of Russian anti-influenza agents in cell culture and animal models]
Autor:
I A, Leneva, I T, Fediakina, M Iu, Eropkin, N V, Gudova, A A, Romanovskaia, D M, Danilenko, S M, Vinogradova, A Iu, Lepeshkin, A M, Shestopalov
Publikováno v:
Voprosy virusologii. 55(3)
The study of the antiviral activity of Russian anti-influenza agents in the cultured MDCK cells demonstrated that arbidol and ribavirin inhibited the reproduction of various influenza A virus strains, including rimantadine- and ozeltamivir-resistant
Autor:
S. M. Vinogradova, S. D. Sokolov, M. D. Mashkovskii, O. G. Azarevich, M. V. Berg, B. A. Medvedev
Publikováno v:
Pharmaceutical Chemistry Journal. 25:864-868
Autor:
M D, Mashkovskiĭ, S D, Iuzhakov, S M, Vinogradova, S D, Sokolov, N N, Suvorov, L Kh, Vinograd, V I, Shvedov
Publikováno v:
Vestnik Rossiiskoi akademii meditsinskikh nauk. (11)
Results of search for new beta-adrenoreceptor blocking agents of different effects are summarized. Derivatives of 4-hydroxyindolyl-3-acetic acid are characterized by a prolonged beta-adrenoblocking effect, cardioselective beta-adrenoblockers were fou
Publikováno v:
Chemistry of Heterocyclic Compounds. 16:506-511
The reaction of 2- and 4-vinylpyridines with 3-substituted phenacylpyridinium ylids takes place regioselectively with the formation of only 6-substituted 1-pyridyl-3-aroylindolizines. The reaction of the same ylids with dimethyl acetylenedicarboxylat
Autor:
S. D. Yuzhakov, M. D. Mashkovskii, M. V. Berg, S. M. Vinogradova, V. N. Ermakova, S. D. Sokolov
Publikováno v:
Pharmaceutical Chemistry Journal. 18:30-36
Autor:
N. S. Bogdanova, V. S. Ignatov, I. S. Nikolaeva, S. D. Sokolov, V. V. Paramonova, G. N. Pershin, S. M. Vinogradova
Publikováno v:
Pharmaceutical Chemistry Journal. 15:854-857
Publikováno v:
Chemistry of Heterocyclic Compounds. 16:997-1000
The indicated compounds are reduced on a dropping-mercury electrode in aqueous alcohol solutions at pH > 7 in one two-electron wave to 1,2-disubstituted hydrazines; four-electron reduction with the formation of amines takes place in acidic media. Two