Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Anatolii R. Syniugin"'
Autor:
Galyna P. Volynets, Fabian Barthels, Stefan J. Hammerschmidt, Olena V. Moshynets, Sergiy S. Lukashov, Sergiy A. Starosyla, Hanna V. Vyshniakova, Olga S. Iungin, Volodymyr G. Bdzhola, Andrii O. Prykhod’ko, Anatolii R. Syniugin, Vladislav M. Sapelkin, Sergiy M. Yarmoluk, Tanja Schirmeister
Publikováno v:
The Journal of Antibiotics. 75:321-332
Staphylococcus aureus is one of the most dangerous pathogens commonly associated with high levels of morbidity and mortality. Sortase A is considered as a promising molecular target for the development of antistaphylococcal agents. Using hybrid virtu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9070f741f09bac54f92b8fed82646a1
https://doi.org/10.1038/s41429-022-00524-8
https://doi.org/10.1038/s41429-022-00524-8
Autor:
Galyna P, Volynets, Mariia O, Usenko, Olga I, Gudzera, Segiy A, Starosyla, Anatoliy O, Balanda, Anatolii R, Syniugin, Oksana B, Gorbatiuk, Andrii O, Prykhod'ko, Volodymyr G, Bdzhola, Sergiy M, Yarmoluk, Michael A, Tukalo
Publikováno v:
Future medicinal chemistry. 14(17)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::edcd957f6e47ed126447b0677cf8aeef
https://pubmed.ncbi.nlm.nih.gov/35876255
https://pubmed.ncbi.nlm.nih.gov/35876255
Autor:
Sergiy M. Yarmoluk, Anatolii R. Syniugin, Galyna P. Volynets, Volodymyr G. Bdzhola, N. O. Kachaput, I. M. Koleiev, M. V. Protopopov, L. V. Pletnova, V. M. Sapelkin, V. I. Matiushok, Sergiy A. Starosyla
Publikováno v:
Biopolymers and Cell. 36:348-357
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::362f737a6ba25c8616c9fc92c62362f7
https://doi.org/10.7124/bc.000a38
https://doi.org/10.7124/bc.000a38
Autor:
Maksym O. Chekanov, Dmytro O. Tverdiy, Andrey A. Fokin, Anatolii R. Syniugin, Sergiy M. Yarmoliuk, Pavlo V. Savitskiy
Publikováno v:
Synthesis. 48:4269-4277
We report a novel and efficient approach to the synthesis of imidazo[1,5-a]pyridine-1-carboxylic acids. By using the reaction of 2-(aminomethyl)pyridine with acyl chlorides followed by one-pot treatment with trifluoroacetic anhydride, 2,2,2-trifluoro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::688e8e741525676e5650bf5ed10bae0c
https://doi.org/10.1055/s-0035-1561489
https://doi.org/10.1055/s-0035-1561489
Autor:
Anatolii R. Syniugin, Alexander E. Pashenko, Maksym O. Chekanov, Sergiy M. Yarmoluk, Andrey A. Fokin, Pavel V. Savitskiy, Tatyana S. Zhuk
Publikováno v:
Tetrahedron Letters. 57:213-215
Intramolecular cyclization of [2-(2-chloroquinolin-3-yl)ethyl]amines, formed in situ from the reaction of N-phthaloyl-protected [2-(2-chloroquinolin-3-yl)ethyl]amines and hydrazine hydrate gave pyrrolo[2,3-b]dihydroquinolines in high yields.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c0ec7608d9167a13f25a13db4f6ef897
https://doi.org/10.1016/j.tetlet.2015.12.011
https://doi.org/10.1016/j.tetlet.2015.12.011
Autor:
Galyna P. Volynets, Anatolii R. Syniugin, Maksym O. Chekanov, Sergiy A. Starosyla, Olga V. Ostrynska, Volodymyr G. Bdzhola, Sergiy M. Yarmoluk
Publikováno v:
Journal of enzyme inhibition and medicinal chemistry. 31(sup4)
In this article, the derivatives of 3-quinoline carboxylic acid were studied as inhibitors of protein kinase CK2. Forty-three new compounds were synthesized. Among them 22 compounds inhibiting CK2 with IC50 in the range from 0.65 to 18.2 μM were ide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c77ff82436fcb2d65c39cb17e9705fb
https://pubmed.ncbi.nlm.nih.gov/27590574
https://pubmed.ncbi.nlm.nih.gov/27590574
Autor:
Andrey A. Fokin, Sergiy M. Yarmoluk, Pavel V. Savitskiy, Anatolii R. Syniugin, Alexander E. Pashenko, Tatyana S. Zhuk, Maksym O. Chekanov
Publikováno v:
ChemInform. 47
Intramolecular cyclization of (quinolin-3-yl)ethylamines, formed in situ via deprotection of the N-phthaloyl derivatives (I), affords title compounds (II) (9 examples) in good to high yields.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9a4b71155d6d1dc6b20c33628fd52400
https://doi.org/10.1002/chin.201619150
https://doi.org/10.1002/chin.201619150