Zobrazeno 1 - 8
of 8
pro vyhledávání: '"V. O. Sinenko"'
Autor:
Vlasyslav Buldenko, Oleksandr L. Kobzar, Yuriy Shulha, Andriy I. Vovk, Diana Hodyna, Stepan G. Pilyo, Volodymyr Brovarets, V. O. Sinenko
Publikováno v:
Ukr. Bioorg. Acta 2020, Vol. 15, N2. 15:33-40
Thiazole-containing derivatives of rhodanine-3-alkanoic acids with propanoic or undecanoic acid groups were synthesized and evaluated as inhibitors of some protein tyrosine phosphatases and glutathione S-transferases. The rhodanines bearing longer ca
Autor:
Larysa Metelytsia, Volodymyr Brovarets, Volodymyr Blagodatny, V. O. Sinenko, Ivan V. Semenyuta, Gennady Poda, S. R. Slivchuk, Diana Hodyna, Vasyl Kovalishyn
Publikováno v:
Current Drug Discovery Technologies. 17:365-375
Background: Tuberculosis (TB) is an infection disease caused by Mycobacterium tuberculosis (Mtb) bacteria. One of the main causes of mortality from TB is the problem of Mtb resistance to known drugs. Objective: The goal of this work is to identify po
Autor:
Oleksandr L. Kobzar, O.P. Trokhimenko, Vasyl Kovalishyn, O.V. Muzychka, V. O. Sinenko, Diana Hodyna, S. R. Slivchuk
Publikováno v:
Reports of the National Academy of Sciences of Ukraine. :70-77
Autor:
Gennady Poda, Diana Hodyna, V. O. Sinenko, Larysa Metelytsia, Julie Grouleff, Vasyl Kovalishyn, S. R. Slivchuk, Igor V. Tetko, Ivan V. Semenyuta, Volodymyr Brovarets, Volodymyr Blagodatny
Publikováno v:
Chem. Biol. Drug Des. 92, 1272-1278 (2018)
The problem of designing new antitubercular drugs against multiple drug‐resistant tuberculosis (MDR‐TB) was addressed using advanced machine learning methods. As there are only few published measurements against MDR‐TB, we collected a large lit
Publikováno v:
Current Chemistry Letters, Vol 7, Iss 1, Pp 1-8 (2018)
The reaction of lithiation of 2-bromo-4-(1,3-dioxolan-2-yl)-1,3-thiazole with in position 5 of the thiazole ring and double lithiation with t-butyllithium (t-BuLi) in positions 2 and 5 lithium diisopropylamide (LDA) are investigated. When lithiated a
Publikováno v:
Russian Journal of General Chemistry. 87:2766-2775
H-Lithiation and Br-lithiation reactions of 1,3-thiazole were studied in order to obtain new thiazole derivatives. Four isomeric chloromethyl derivatives of 1,3-thiazole containing a protected aldehyde group like 2-(1,3-dioxolan-2-yl)-5-(chloromethyl
Publikováno v:
Russian Journal of General Chemistry. 86:1597-1603
Reactions of substituted 2-hydroxyalkyl-1,3-thiazole-5-carbaldehydes and 5-hydroxyalkyl-1,3-thiazole-2-carbaldehydes with phenylhydrazine, isoniazid, N-substituted rhodanines were performed as well as Biginelli reaction with acetoacetic ester and ure
Publikováno v:
Russian Journal of General Chemistry. 85:1855-1861
A general approach towards synthesis of 2(5)-hydroxyalkyl-substituted 1,3-thiazole derivatives has been proposed. The method includes lithiation of 1,3-thiazole ring followed by reacting the formed thiazole lithium derivatives with electrophiles.