Zobrazeno 1 - 10
of 99
pro vyhledávání: '"N. A. Bragina"'
Publikováno v:
Российский кардиологический журнал, Vol 0, Iss 4, Pp 7-13 (2018)
Aim. Assessment of prognostic significance of endothelial dysfunction markers: stable metabolites of nitric oxide (NOx), von Willebrand factor (vWF), endothelin-1 (E1), homocysteine and tissue plasminogen activator (tPA) in essential hypertension (EA
Externí odkaz:
https://doaj.org/article/8ea9f90e9eb84800aa8cd29334a180d5
Publikováno v:
Тонкие химические технологии, Vol 13, Iss 2, Pp 21-30 (2018)
This work is dedicated to the synthesis of porphyrin metal complexes for creation of dyesensitized solar cells (DSSC). Three different dyes were synthesized - zinc complexes of porphyrins containing alkoxyl substituents: with symmetric structure (Zn-
Externí odkaz:
https://doaj.org/article/20845435857048b8bcb5c7b4ee1d6bd0
Publikováno v:
Тонкие химические технологии, Vol 7, Iss 5, Pp 28-33 (2012)
In this paper we report the synthesis donor - acceptor systems based on fullerene C60 and lipophilic meso - arylporphyrins . The obtained conjugates were characterized by IR, UV-vis,1H,13C NMR spectroscopy and MALDI-TOF mass spectrometry. The fluores
Externí odkaz:
https://doaj.org/article/e4f00ad8190747cc926b7edb043638ba
Publikováno v:
Тонкие химические технологии, Vol 4, Iss 6, Pp 52-55 (2009)
The organization and methodical support of the theoretical education of the graduate students specializing in the «Bioorganic chemistry» and «Biotechnology» are presented. Experience accumulated upon teaching the graduate students on the Departme
Externí odkaz:
https://doaj.org/article/b39991401c50440496c3c912a0b7e532
Autor:
N. V. Novikov, V. V. Starkov, K. A. Formirovskiy, N. A. Bragina, I. P. Ushakova, A. F. Mironov
Publikováno v:
Тонкие химические технологии, Vol 4, Iss 4, Pp 26-30 (2009)
Synthesis of amphyphilic cationic meso-pyridilsubstituted porphyrins bearing long chain alkyl groups is described. An improved methods of preparation of tetra- and mono-alkylsubstituted meso-pyridil porphyrins are proposed. The data porphyrins will b
Externí odkaz:
https://doaj.org/article/b7a887d36a044c15a63e653c164e1348
Publikováno v:
Тонкие химические технологии, Vol 3, Iss 2, Pp 74-78 (2008)
Synthesis of 1,2-di-(11,13-tetradecadienoyl)-sn-glycero-3-phosphocholine and 1,2-di- (2,4-hexadienoyl)-sn-glycero-3-phosphocholine, containing terminal polymerizable diene groups has been carried out. It is supposed that using of synthesized phosphor
Externí odkaz:
https://doaj.org/article/2c9ed7875f1d403d80348792951d613d
Autor:
I. N. Fedulova, N. V. Novikov, O. A. Ugolnikova, N. A. Bragina, I. P. Ushakova, A. F. Mironov
Publikováno v:
Тонкие химические технологии, Vol 2, Iss 4, Pp 83-89 (2007)
Synthesis of amphiphilic meso-arylsubstituted porphyrins with hydrophobic long chain groups and with terminal carboxylic and hydroxylic groups via dipyrrolylmethanes and with the use of monopyrrolic condensation is described. The synthesized porphyri
Externí odkaz:
https://doaj.org/article/735eca27e31a467a867748dfffabacac
Publikováno v:
Тонкие химические технологии, Vol 1, Iss 4, Pp 67-70 (2006)
Synthesis of meso-arylsubstituted porphyrins with hydrophobic long chain groups by using the dipyrromethanes method and monopyrrolic condensation is described. Data lypoporphyrins possess liquid crystalline properties and will be used to design supra
Externí odkaz:
https://doaj.org/article/2d1f17c12c89491f9a23c008d3b9746f
Publikováno v:
Тонкие химические технологии, Vol 1, Iss 1, Pp 50-52 (2006)
Synthesis of meso-arylsubstituted dipyrromethanes with hydrophobic long chain groups and their application in the synthesis of trans-substituted tetraphenylporphyrins are described. The data lypoporphyrins will be investigated in the structure of mod
Externí odkaz:
https://doaj.org/article/be310642972e4085a66aa0243deaf939
Publikováno v:
Вестник интенсивной терапии, Iss 4 (2023)
ЦЕЛЬ ИССЛЕДОВАНИЯ: Описать имеющиеся данные о показаниях, осложнениях, реализации и альтернативных стратегиях использования физическо
Externí odkaz:
https://doaj.org/article/b8862910defa43a99b35dc32dca36054