Zobrazeno 1 - 10 of 85 pro vyhledávání: '"T. S. Stytsenko"'
1
Akademický článek
Optimization of the 9α-hydroxylation of steroid substrates using an original culture of Rhodococcus erythropolis
Autor: V. A. Andryushina, N. V. Karpova, T. S. Stytsenko, V. V. Yaderets, E. D. Voskresenskaya, V. V. Dzhavakhia
Publikováno v: Regulatory Mechanisms in Biosystems, Vol 9, Iss 3, Pp 430-434 (2018)
To obtain inoculation material (cultivation stage 1), the biomass of Rhodococcus erythropolis VKPM AC-1740 was transferred from agar slants into 750 ml conic flasks containing 100 ml of vegetation media of the following composition (g/l): medium 1
Externí odkaz: https://doaj.org/article/c8cfcbc6b03c4874a7beb3dad428df17
Zobrazit plný text záznamu
2
Study of biotransformation of cholesterol 3β-methyl ether by mycobacteria Mycobacterium sp
Autor: I. V. Zavarzin, V. V. Yaderets, D. V. Kurilov, T. S. Stytsenko, N. V. Karpova, V. A. Andryushina
Publikováno v: Russian Chemical Bulletin. 70:533-538
The influence of exogenous factors on the selectivity of biotransformation of cholesterol 3β-methyl ether by Mycobacterium sp. was studied. The main product of the microbiological transformation was Δ5-dehydroepiandrosterone 3β-methyl ether. The p
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::078045ead7cad3d316a2e072489f92d4
https://doi.org/10.1007/s11172-021-3120-8
Zobrazit plný text záznamu
3
Preparation of Plant and Animal Sterol Ethers and Esters as Key Intermediates for the Synthesis of Dehydroepiandrosterone
Autor: N. V. Karpova, V. V. Dzhavakhiya, V. V. Yaderets, T. S. Stytsenko, V. A. Andryushina
Publikováno v: Pharmaceutical Chemistry Journal. 53:1086-1089
Series of cholesterol and β-sitosterol ethers and esters were obtained and could be used for subsequent enzymatic cleavage of the steroid C-17 side chain to dehydroepiandrosterone using mycobacteria cultures.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e9a0806bed0d4a0b04d367bb1c08843f
https://doi.org/10.1007/s11094-020-02127-9
Zobrazit plný text záznamu
4
Synthesis of 3β-methyl ether of dehydroepiandrosterone by biotransformation of 3β-methyl ether of cholesterol with cells of mycobacteria Mycobacterium sp
Autor: T. S. Stytsenko, I. V. Zavarzin, V. V. Yaderets, D. V. Kurilov, V. A. Andryushina, N. V. Karpova
Publikováno v: Russian Chemical Bulletin. 68:2355-2358
3p-Methyl ether of dehydroepiandrosterone was obtained by microbiological transformation of 3s-methyl ether of cholesterol with Mycobacterium sp. Androstane-3,17-dione, androst-4-ene-3,17-dione, and androsta-1,4-diene-3,17-dione were minor transforma
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::de17101d3b2563aae174cf8b71fff732
https://doi.org/10.1007/s11172-019-2711-0
Zobrazit plný text záznamu
5
Optimization of the Method of Obtaining 9α-Hydroxy-androst-4-ene-3,17-dione—the Key Intermediate in the Synthesis of Highly Active Fluorinated Corticosteroids from Phytosterols
Autor: N. V. Karpova, V. V. Dzhavakhiya, T. S. Stytsenko, V. V. Yaderets, V. A. Andryushina
Publikováno v: Applied Biochemistry and Microbiology. 55:37-40
A method of phytosterol conversion into 9α-hydroxy-androstenedione under high loads of steroid substrate has been developed with the use of mixed cultures of the actinobacteria M. neoaurum and R. erythropolis. The introduction of a 9α-hydroxylating
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::9097373b8d8b298978a8aa3f0e95c31e
https://doi.org/10.1134/s0003683819010071
Zobrazit plný text záznamu
6
Efficient Synthesis of 21-Acetoxypregna-1,4,9(11),16-Tetraene-3,20-Dione, a Key Intermediate in the Synthesis of Highly Active Fluorinated Corticosteroids from 9α-Hydroxyandrostenedione
Autor: T. S. Stytsenko, V. A. Andryushina, V. V. Yaderets, N. V. Karpova, V. V. Dzhavakhiya
Publikováno v: Pharmaceutical Chemistry Journal. 52:776-780
An efficient synthesis of 21-acetoxypregna-1,4,9(11),16-tetraene-3,20-dione, a key intermediate in the synthesis of highly active fluorinated corticosteroids from phytosterols, was developed. The method consisted of an original sequence of chemical a
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1f871d56f839789d996de3cb4e46104b
https://doi.org/10.1007/s11094-018-1898-y
Zobrazit plný text záznamu
7
A search for microscopic fungi with directed hydroxylase activity for the synthesis of steroid drugs
Autor: A. V. Kurakov, T. S. Stytsenko, V. A. Andryushina, N. V. Karpova, T. D. Feofanova, A. V. Druzhinina
Publikováno v: Applied Biochemistry and Microbiology. 52:316-323
The hydroxylase activities of new strains such as Curvularia lunata, C. geniculata, C. eragrostidis, C. prasadii, Ulocladium botrytis, Alternaria tenuis, and Fusarium oxysporum toward three steroid substrates, namely, androstenedione (AD), cortexolon
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::12b1b94906220f95215ee14cda636aa0
https://doi.org/10.1134/s000368381603008x
Zobrazit plný text záznamu
9
Novel immobilized biocatalyst for microbiological synthesis of pharmaceutical steroids
Autor: T. S. Stytsenko, A. N. Ryabev, A. V. Druzhinina, E. A. Podorozhko, Vladimir I. Lozinsky, V. A. Andryushina, N. V. Karpova
Publikováno v: Applied Biochemistry and Microbiology. 51:530-538
The steroid-transforming activity of free and immobilized cells of Pimelobacter simplex VKPM Ac-1632 entrapped in an operationally stable macroporous poly(vinyl alcohol) cryogel was studied. It was shown that the macroporous matrix of the carrier did
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::a2a198a72ce933450eac77997fd9cc7b
https://doi.org/10.1134/s0003683815050026
Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání

Omezení vyhledávání
Plný text Recenzováno Digitální knihovna AV ČR
Zdroje