Zobrazeno 1 - 10
of 670
pro vyhledávání: '"Mirskova, A. N."'
Autor:
Pavlova, Olga N. ⁎, Adamovich, Sergey N., Novikova, Angelina S., Gorshkov, Alexander G., Izosimova, Oksana N., Ushakov, Igor A., Oborina, Elizaveta N., Mirskova, Anna N., Zemskaya, Tamara I.
Publikováno v:
In Biotechnology Reports December 2019 24
Publikováno v:
Open Chemistry, Vol 13, Iss 1 (2014)
Externí odkaz:
https://doaj.org/article/2226e8c2d3dc4f24bd761a5a250097dd
Autor:
Adamovich, S. N.1,2, Mirskova, A. N.1, Zel'bst, E. A.3 zelbst@rambler.ru, Fundamensky, V. S.4
Publikováno v:
Journal of Structural Chemistry. May2018, Vol. 59 Issue 3, p707-710. 4p.
Publikováno v:
Journal of Structural Chemistry. 59:707-710
The crystal structure of a new compound Ca(4-ClC6H4SCH2COO)2·Н2О obtained as a part of the study of biologically active metal protatranes is determined by single crystal X-ray diffraction. The coordination polyhedron of the calcium atom is heptaco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::17c04ee159b4541d138f1b567e60a757
https://doi.org/10.1134/s0022476618030319
https://doi.org/10.1134/s0022476618030319
Synthesis and Pharmacological Activity of Tris(2-hydroxyethyl)ammonium 4-Chlorophenylsulfonylacetate
Publikováno v:
Russian Journal of Applied Chemistry. 91:701-705
Methods for the synthesis of 4-chlorophenylsulfonylacetic acid and its tris(2-hydroxyethyl)ammonium salt (“sulfacetamine”) were studied. The results of in vitro and in vivo experiments showed that sulfacetamine possesses high antithrombotic, anti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8c6829944e9d0b03eb0471a4af747fe7
https://doi.org/10.1134/s1070427218040249
https://doi.org/10.1134/s1070427218040249
Autor:
Sergey N. Adamovich, Mirskova Anna N
Publikováno v:
Russian Journal of Applied Chemistry. 91:469-472
Difficultly accessible 1-R-indol-3-ylsulfanyl(sulfonyl)acetic acids 1-R-IndYCH2CO2H (R = H, Me, Bn; Y = S, SO2) 1a–Id were prepared. Their reaction with tris(2-hydroxyethyl)amine yielded tris(2-hydroxyethyl) ammonium 1-R-indol-3-ylsulfanyl(sulfonyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d8af620c4f7f83519b5b27495ae82c1b
https://doi.org/10.1134/s1070427218030205
https://doi.org/10.1134/s1070427218030205
Publikováno v:
Journal of Structural Chemistry. 58:1468-1471
Sulfones are known to be biologically active compounds. X-ray diffraction is used to determine the crystal and molecular structure of methyl-(4-chlorophenyl)sulfone. The closest molecules are in pairs oriented to each other by their chlorine atoms. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::87d65dea4bfe2615ba8b9031f3db7999
https://doi.org/10.1134/s0022476617070307
https://doi.org/10.1134/s0022476617070307
Autor:
Adamovich, Sergei N., Ushakov, Igor A., Mirskova, Anna N., Mirskov, Rudolf G., Voronov, Vladimir K.
Publikováno v:
In Mendeleev Communications September-October 2014 24(5):293-294
Publikováno v:
Russian Chemical Bulletin. 66:1320-1324
A number of tris(2-hydroxyethyl)ammonium arylchalcogenylacetates ArYCH2CO2–• •HN+(CH2CH2OH)3 (1—4) (Ar = aryl; Y = O, S, SO2) were synthesized. Their structure was established by IR and 1H, 13C, 15N NMR spectroscopy. The influence of compound
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::055c6762407b3b2e60cf27c4ed233838
https://doi.org/10.1007/s11172-017-1893-6
https://doi.org/10.1007/s11172-017-1893-6
Autor:
Tamara I. Zemskaya, Sergey N. Adamovich, Igor A. Ushakov, O.N. Izosimova, A. S. Novikova, Mirskova Anna N, A. G. Gorshkov, O. N. Pavlova, E. N. Oborina
Publikováno v:
Biotechnology Reports
Biotechnology Reports, Vol 24, Iss, Pp-(2019)
Biotechnology Reports, Vol 24, Iss, Pp-(2019)
Highlights • We have synthesized a wide range of tris-(2-hydroxyethyl)ammonium arylchalcogenylacetates, “protatranes”. • “Protatranes” are growth stimulators of hydrocarbon-oxidizing Rhodococcus erythropolis bacteria isolated from Lake Ba
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46a70b27d3ed6fb9cd6ea66876169d0a
http://europepmc.org/articles/PMC6732725
http://europepmc.org/articles/PMC6732725