Zobrazeno 1 - 10
of 30
pro vyhledávání: '"A. N. Evstropov"'
Publikováno v:
Бюллетень сибирской медицины, Vol 1, Iss 4, Pp 27-31 (2002)
In the present work the antiviral activity of water extract, received from Pеnthaphylloides fruticosa (L.) O. Scwarz, against Enteroviruses Coxsackie B (CVB) was studied. The maximal intoxic dose of the preparation for the cell-culture (CC) Нер-2
Externí odkaz:
https://doaj.org/article/eae53ca4fe3b446884fa7eef0a9981b6
Autor:
Anastasia I. Parakhina, Larisa I. Parakhina, Darya A. Troshina, Katerina E. Levina, Yulia A. Pimenova, Elena N. Koteneva, Aleksandr N. Evstropov, Liudmila N. Zakharova, Andrey Yu. Mironov, Tatyana G. Suranova
Publikováno v:
Epidemiology and Infectious Diseases. 27:280-289
BACKGROUND: Resistance of microorganisms to antimicrobial drugs (AMP) is one of the global problems of modern medicine, which poses a serious threat to human health. The formation of the resistance of pathogens to AMP forces us to look for new ways t
Autor:
D. V. Reshetnikov, L. G. Burova, T. V. Rybalova, E. A. Bondareva, S. S. Patrushev, A. N. Evstropov, E. E. Shults
Publikováno v:
Chemistry of Natural Compounds. 58:908-915
Autor:
Tatyana V. Rybalova, Alexander N. Evstropov, Lyubov G. Burova, Elvira E. Shults, Anna A. Shtro, Il’ya V. Shirokikh, Dmitry S. Baev, Sergey S. Patrushev
Publikováno v:
Letters in Drug Design & Discovery. 18:686-700
Background: Natural sesquiterpene lactones are an important class of heterocyclic compounds in drug discovery since they possess a wide range of biological properties, including antibacterial activity. Objective: The objective of this study was to sy
Autor:
Alla V. Lipeeva, Danila O. Zakharov, Liubov G. Burova, Tatyana S. Frolova, Dmitry S. Baev, Ilia V. Shirokikh, Alexander N. Evstropov, Olga I. Sinitsyna, Tatyana G. Tolsikova, Elvira E. Shults
Publikováno v:
Molecules, Vol 24, Iss 11, p 2126 (2019)
Synthesis of 1,2,3-triazole-substituted coumarins and also 1,2,3-triazolyl or 1,2,3-triazolylalk-1-inyl-linked coumarin-2,3-furocoumarin hybrids was performed by employing the cross-coupling and copper catalyzed azide-alkyne cycloaddition reaction ap
Externí odkaz:
https://doaj.org/article/b3ec096e033f4bf7b50bb3586caaef2f
Publikováno v:
Сахарный диабет, Vol 2, Iss 4, Pp 15-18 (1999)
Актуальность. Большой интерес представляют исследования о роли ИФН в патогенезе СД и его осложнений. При аберрантной экспрессии генов HL
Externí odkaz:
https://doaj.org/article/a17a70b42d8540019c7055e88efe253a
Autor:
Alexander N. Evstropov, Olga I. Sinitsyna, Ilia V. Shirokikh, Liubov G. Burova, Dmitry S. Baev, Danila O. Zakharov, A. V. Lipeeva, Elvira E. Shults, Tatyana G. Tolsikova, T. S. Frolova
Publikováno v:
Molecules, Vol 24, Iss 11, p 2126 (2019)
Molecules
Volume 24
Issue 11
Molecules
Volume 24
Issue 11
Synthesis of 1,2,3-triazole-substituted coumarins and also 1,2,3-triazolyl or 1,2,3-triazolylalk-1-inyl-linked coumarin-2,3-furocoumarin hybrids was performed by employing the cross-coupling and copper catalyzed azide-alkyne cycloaddition reaction ap
Autor:
T N, Elkina, L N, Zakharova, A N, Evstropov, I O, Marinkin, I A, Nesina, A A, Liutkevich, Z P, Khudonogova, M V, Sholar', M G, Pustovetova, V I, Grachev, O A, Gribanova, Iu A, Tatarenko
Publikováno v:
Voprosy kurortologii, fizioterapii, i lechebnoi fizicheskoi kultury. (6)
A series of investigations have demonstrated the anti-inflammatory, bactericidal, analgesic, and vegetocorrective effects of extraocular selective polarized chromotherapy using blue and red light and the possibility to optimize autonomous regulation
Publikováno v:
Сахарный диабет, Vol 2, Iss 4, Pp 15-18 (1999)
Актуальность. Большой интерес представляют исследования о роли ИФН в патогенезе СД и его осложнений. При аберрантной экспрессии генов HL
Autor:
V. E. Yavorovskaya, A. N. Evstropov, Yu. Yu. Straukas, N. Dirvyanskite, V. N. Kiseleva, R. Yankauskas
Publikováno v:
Pharmaceutical Chemistry Journal. 30:231-234
As was shown in a previous publication [I], both the Nacyl and O-acyl derivatives ofthreo-DL-phenylserine possess antiviral activity in vitro and are capable, in the maximum tolerable dose, of completely inhibiting reproduction of the A2 influenza vi